Next Article in Journal
Effects of Transgenic Insect-Resistant Maize HGK60 on Rhizosphere Soil Bacterial Communities
Previous Article in Journal
Investigating the Alleviating Effects of Dihydromyricetin on Subclinical Mastitis in Dairy Cows: Insights from Gut Microbiota and Metabolomic Analysis
Previous Article in Special Issue
Diversity, Composition, and Ecological Function of Endophytic Fungal Communities Associated with Erigeron breviscapus in China
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Bioeconomy-Based Approaches for the Microbial Valorization of Citrus Processing Waste

by
Ioannis Stavrakakis
1,
Paraschos Melidis
1,
Nektarios Kavroulakis
2,
Michael Goliomytis
3,
Panagiotis Simitzis
3 and
Spyridon Ntougias
1,*
1
Laboratory of Wastewater Management and Treatment Technologies, Department of Environmental Engineering, Democritus University of Thrace, Vas. Sofias 12, 67132 Xanthi, Greece
2
Institute for Olive Tree, Subtropical Plants and Viticulture, Hellenic Agricultural Organization—Dimitra (ELGO-DIMITRA), Agrokipio-Souda, 73164 Chania, Greece
3
Laboratory of Animal Breeding and Husbandry, Department of Animal Science, Agricultural University of Athens, 75 Iera Odos, 11855 Athens, Greece
*
Author to whom correspondence should be addressed.
Microorganisms 2025, 13(8), 1891; https://doi.org/10.3390/microorganisms13081891
Submission received: 6 June 2025 / Revised: 9 August 2025 / Accepted: 12 August 2025 / Published: 13 August 2025
(This article belongs to the Special Issue Earth Systems: Shaped by Microbial Life)

Abstract

The citrus processing industry is an economically important agro-industrial sector worldwide; however, it produces significant amounts of waste annually. The biorefinery concept and the recovery of bio-based materials from agro-industrial residues, including citrus processing waste, are emphasized in the European Green Deal, reflecting the EU’s commitment to fostering circularity. Biotreatment of citrus processing waste, including bioconversion into biomethane, biohydrogen, bioethanol and biodiesel, has been applied to valorize biomass for energy recovery. It can also be composted into a valuable soil conditioners and fertilizers, while raw and fermented citrus residues may exhibit phytoprotective activity. Citrus-derived residues can be converted into materials such as nanoparticles with adsorptive capacity for heavy metals and recalcitrant organic pollutants, and materials with antimicrobial properties against various microbial pathogens, or the potential to remove antibiotic-resistance genes (ARGs) from wastewater. Indeed, citrus residues are an ideal source of industrial biomolecules, like pectin, and the recovery of bioactive compounds with added value in food processing industry. Citrus processing waste can also serve as a source for isolating specialized microbial starter cultures or as a substrate for the growth of bioplastic-producing microorganisms. Solid-state fermentation of citrus residues can enhance the production of hydrolytic enzymes, with applications in food and environmental technology, as well as in animal feed. Certain fermented products also exhibit antioxidant properties. Citrus processing waste may be used as alternative feedstuff that potentially improves the oxidative stability and quality of animal products.

1. Citrus Processing Waste

The citrus processing industry is an economically important sector worldwide and a key agro-industrial sector in the Mediterranean region. In particular, China, the Mediterranean countries, Brazil, India, the United States and Mexico produce more than 80% of the world’s citrus crops, with orange being the most abundant citrus fruit in the globe [1] (Figure 1).
As a consequence, a massive amount of waste is generated annually by the citrus processing industry, which is characterized by high content of pectin, cellulose and hemicellulose. The peel portion of various citrus fruits and the key bioactive compounds as well as pectin, lignocellulose and lipid/fat content of the peels of the major citrus crops are illustrated in Table 1.
For instance, orange peels contain a high pectin content, followed by hemicellulose and cellulose, each constituting nearly 10% of the composition, whereas soluble sugars represent up to 7% of the content [37]. Moreover, D- limonene and hesperidin are the key bioactive compounds found in the peels of the major citrus crops (Table 1).
Thus, more than 60 million tons of citrus waste are generated annually worldwide by this agro-industrial sector [49]. In Greece, more than one million tons of citrus fruits, with most of them being oranges, were produced in 2023 [1], of which approximately half were considered as food waste. Land disposal of untreated citrus processing waste may induce adverse effects on soil, compromising soil fertility and health [50]. Orange processing waste disposal can induce detrimental effects on soil fauna, e.g., on the earthworm Lumbricus terrestris [50]. Due to citrus processing waste decomposition, the rich in organic matter leachate generated by heavy rainfall can lead to increased total suspended solids and under certain circumstances, to oxygen depletion in local aquatic bodies [51]. Soil dumping of citrus processing waste can also result in pH decrease, affecting soil microbial community structure and nutrient cycling processes [51]. The presence of residual pesticides in citrus crops [52] may further affect soil fertility and quality if the waste is improperly disposed off. Thus, proper treatment of citrus processing waste is required to prevent soil deterioration and improve soil health for sustainable land use.

2. Legislative Framework for the Valorization of Citrus Processing Waste in the EU

The current EU strategy towards sustainable use of organic waste as input material, shifting from a linear to a circular economy and bioeconomy model in food waste management and valorization. Towards a circular economy—waste management of food waste in the EU, anaerobic digestion for energy and fuels is “near the bottom of the bio-refining value pyramid” [53], whereas the recovery of high value-added substrates and biological agents for enhanced plant productivity as well as for improved food and animal feed is positioned on the top of the pyramid. Thus, the vast streams of citrus processing wastes should be valorized within the circular economy prism.
The Circular Economy Action Plan [54], as part of the European Green Deal, prioritizes the valorization of bio-waste, with a particular focus on the food industry and food supply chain sectors. Biorefineries’ concept and recovery of bio-based materials from agro-industrial by-products and residues are prominently featured in European Green Deal, reflecting the EU’s commitment to fostering a circular bioeconomy. In this direction, the EU Bioeconomy Strategy encourages local bioeconomy development through the sustainable use of biological resources, unlocking the biotechnological potential of microbial inocula to produce innovative products and converting the wastes and by-products of the agri-food sector into high value-added products. In alignment with the implementation of Fertilizing Products Regulation (Regulation (EU) 2019/1009) [55] and Animal By-Products Regulation (Regulation (EC) No 1069/2009) [56], there is a growing need for efficient, cost-effective, green technologies capable of biotransforming citrus processing waste into high value-added products, serving as plant-protective agents in sustainable agriculture, as well as a safe and nutritionally valuable component in animal feed. Although EU policy through the Green Deal supports circular bioeconomy approaches in valorizing citrus processing waste, practical implementation of such methods faces barriers, like regulatory uncertainty, misaligned incentives and lengthy product safety approvals for food and feed, as well as for biobased materials, a fact that may increase time to market and overall costs, posing an obstacle for private investors [57].

3. Biomass Valorization of Citrus Processing Waste for Energy Recovery

Anaerobic digestion can be considered as an environmental-friendly bioprocessing approach for citrus processing waste [58,59]. Limonene, a major component of citrus essential oils, can pose an obstacle in the anaerobic digestion of such waste due to its inhibitory properties [60]. On the other hand, Jiménez-Castro et al. [61] carried out two-stage anaerobic digestion of orange residues without the need of pretreatment.
Dark fermentation for biohydrogen production is also an alternative treatment method for citrus processing waste [62]. Camargo et al. [63] reported on biohydrogen production from citrus peels through dark fermentation preliminarily carried out by Clostridium and Paraclostridium strains. However, pretreatment steps are often required to enhance biohydrogen production during dark fermentation of citrus processing waste [64]. Indeed, the high essential oil content of citrus processing waste can inhibit its bioconversion to biomethane or biohydrogen, often requiring pretreatment steps that raise operating cost.
Bioethanol is another valuable biomolecule produced during yeast fermentation of citrus processing waste for energy generation [65]. For instance, orange peels were served as immobilization carriers of Saccharomyces yeasts to act as biocatalysts in alcoholic fermentation [66]. However, the removal of D-limonene is still a necessary step to enhance bioethanol yields.
Citrus processing waste can serve as substrate for oleaginous yeasts cultivation for further use in biodiesel production [67]. Cultivation of Candida parapsilosis Y19 on orange peels resulted in increased lipid content and a fatty acid composition consisting of unsaturated fatty acids, mainly oleic acid, suggesting that orange processing residues can serve as suitable substrates for growth of oleaginous yeasts for biodiesel production. In particular, they served as growth substrate for enhanced lipid production during fermentation with the oleaginous yeast C. parapsilosis, reporting total lipids production of 4.78 g/L that corresponded to lipid content in the microbial biomass of 39% [68]. Seeds of Citrus sinensis were also found to be rich in lipids, consisting of 37% of their content, with the lipid fraction comprising linoleic, palmitic and oleic acids [69], making them suitable for biodiesel production.
Bioconversion of citrus processing waste through ensiling can resulting in bioethanol and lactic acid production [70]. In this case, volatile solids and limonene can be reduced by approximately 65% and 75%, respectively, so increasing the anaerobic digestibility of the silage [71]. The main bioenergy recovery approaches from citrus processing waste are presented in Table 2.

4. Bioconversion of Citrus Processing Waste for Enhanced Soil Fertility and Phytoprotective Properties

Biotreated citrus processing waste can enhance soil fertility and induce phytoprotection. It has been found that biotreated citrus waste can improve physical properties, like soil porosity and water retention, as well as nutrient availability, resulted in enhanced microbial activity and population of beneficial microorganisms [72]. Interestingly, Kato-Noguchi and Kato [73] attributed the phytoprotective properties of citrus processing waste against weeds, herbivore insects, parasitic nematodes and phytopathogenic fungi to the direct effects of some compounds of these residues, like essential oils.
Co-composting is an aerobic treatment method for citrus processing waste, in which citrus peels are initially colonized by mesophilic yeasts, followed by thermophilic microbiota, resulting in a mature compost with acceptable phytotoxicity levels [74]. Vermicomposting with the earthworm Eisenia fetida is also a composting approach applied for treating orange processing waste [75]. The application of compost derived from citrus processing waste, following pH adjustment with phosphoric acid, resulted in optimal seedling development in tomato and zucchini at a 7.5% compost-amended substrate [76]. By applying 4 kg of orange waste per square meter of land, Tuttobene et al. [77] found that durum wheat yields were comparable to those achieved with mineral fertilizer.
Citrus processing waste can also be applied in weed management strategies. Shehata et al. [78] found that orange processing waste can contribute to weed control during onion cultivation, reporting double bulb yield. Ugolini et al. [79] found that an orange juice processing residue rich in limonene could inhibit the germination of the weed Chenopodium album and delay the germination in Lactuca sativa in manner that its plant biomass was not affected, thus exhibiting bioherbicidal properties.
Agricultural solid wastes, including citrus processing residues, have shown potential for the adsorption and partial removal of pesticides such as diazinon and parathion. This suggests a possible low-cost, sustainable approach for mitigating pesticide contamination in water and soil systems [80]. Essential oils from citrus processing waste have the potential to be applied as bioinsecticides. For example, Citrus aurantium extract has been used for the phytoprotection of chickpea plants against Callosobruchus maculatus [81]. Essential oils from citrus peels are also capable of preventing post-harvest plant diseases, such as anthracnose induced by Colletotrichum gloeosporioides and C. scovillei [82]. Sala et al. [83] used agro-industrial by-products, including orange peels, as growth substrates for the cultivation of bioprotective fungal agents Beauveria bassiana and Trichoderma harzianum. Even though nutrient immobilization or phytotoxic effects induced by residual essential oils may occur during land application. The bioconversion of citrus processing waste to soil fertility enhancers and phytoprotective agents is illustrated in Table 3.

5. Valorization of Citrus Processing Waste into Biobased Polymers, Antimicrobial Materials, and Adsorbents

Citrus processing waste can be used in sustainable applications within the prism of circular economy [84]. Citrus peels can be used as substrate to enhance the growth of polyhydroxyalkanoate (PHA)-producing microbes for bioplastics production. For instance, a Bacillus cereus strain growing on orange peels produced more than 0.4 g/kg polyhydroxybutyrate (PHB) [85]. A biocomposite consisting of Arabic gum and carboxymethyl cellulose as well as orange peel extract exerted antimicrobial properties against Salmonella enterica and Escherichia coli O157 and high antioxidant activity (0.45 mM Trolox/mg extract), also having ameliorated barrier properties regarding water vapor and oxygen transmission rates [86]. Pagliarini et al. [87] fabricated a biobased polymer composite consisted of poly(butylene succinate-co-adipate) and up to 20% w/w orange peels to be used as natural filler, exhibiting both antioxidant and antibacterial activity. Citrus by-products are also considered as eco-friendly resources for producing functional and smart food packaging [88]. Citrus processing waste essential oils can also be used as antimicrobial agents in food-packaging applications. Interestingly, waste eggshell together with essential oil from orange peels, to act as a bioactive agent, and pectin, has been used to make a biocomposite film [89]. This fabricated film performed effectively under hydrological stress and exhibited antimicrobial properties against Staphylococcus aureus and Bacillus cereus [89]. Moreover, submerged fermentation of orange processing waste using Bacillus haynesii E1 resulted in the production of a biosurfactant compound [90].
Citrus-derived residues can be converted into material with antimicrobial properties against various microbial pathogens. Notably, orange peel extracts have been used for the synthesis of nanoparticles with antimicrobial properties. Kifle et al. [91] recently synthesized silver nanoparticles (AgNPs) using the extract derived from Citrus sinensis peels, exhibiting protecting properties against bacterial pathogens, i.e., Bacillus cereus, Escherichia coli, Morganella morganii and Staphylococcus aureus, and spoilage fungi like Alternaria alternata, Aspergillus niger, Fusarium oxysporum and Penicillium digitatum. Citrus-derived, chitosan-coated, selenium nanocomposite was fabricated and tested as a fungicide against common plant pathogens, such as the fungus Sclerotinia sclerotiorum, resulting in almost complete pathogen suppression at a minimum inhibitory concentration of 0.5 ppm [92].
Citrus processing waste can find applications as adsorbent material to remove heavy metals and recalcitrant organic pollutants. Activated carbon derived from orange peels and modified by TiO2 has been examined in terms of its ability to remove As from water. In particular, a maximum adsorbent capacity of 10.9 mg/g was recorded by applying an adsorbent concentration of 3.3 g/L in the presence of 50 mg As/L, under a treatment time of approximately 5 h and pH 4.2 [93]. Kukowska et al. [94] stated that activated carbon derived from orange peels through microwave furnace activation at 800 °C can serve as an efficient, environmental-friendly adsorbent, reporting arsenic (As) (V), selenium (Se) (IV), copper (Cu) (II) and cadmium (Cd) (II) removal efficiencies greater than 15%, 20%, 98% and 80% when metal concentration of 200 μg/L was treated with 0.02 g orange peel-derived activated carbon. Bouchelkia et al. [95] reported that orange peels can be used as bioadsorbents, resulting in removing approximately 112 mg methylene blue dye/g of adsorbent. Valorization of citrus processing residues can be achieved by converting into innovative nanoporous materials [96]. Orange peels have been utilized to fabricate organometallic adsorbent nanomaterials like ZnO-based orange peel-derived composites (ZnO-NR@PC) to serve as porous material of high adsorbent efficacy and stability, with removal efficiency greater than 90% in the case of the dyes crystal violet and methylene blue [97]. Moreover, biochar made from orange peels was capable of adsorbing extracellular DNA, indicating its potential to reduce the environmental dissemination of antibiotic-resistance genes (ARGs) [98].
Citrus processing residues can also be transformed into high-sensitivity sensors for monitoring pollution. An electrochemical nitrate sensor was developed by using activated carbon derived from orange peels and decorated with Cu2O crystals, displaying a linear response up to 1 mM and a detection limit of 1.2 μM [99]. Moreover, the highly lignocellulosic orange peel waste can also be transformed into innovative acoustic material through ultrasonic treatment [100]. The bioconversion of citrus processing waste to biobased polymers, antimicrobial materials, and adsorbents, is reported in Table 4.

6. Solid-State Fermentation of Citrus Processing Waste for Food and Environmental Processing Applications

Solid-state fermentation of citrus processing waste has gained ground for various applications in food and environmental technology (Table 5). A biorefinery approach to valorize orange peels by extracting essential oils, i.e., limonene, and recovering high-activity peroxidase, while bioconverting the remaining cellulose via enzymatic hydrolysis into lactic acid and the bioplastic polyhydroxybutyrate using Weizmannia coagulans and Priestia megaterium, respectively, was conducted by Mihalyi et al. [101]. Mondal et al. [102] also reported on the enzymatic bioconversion of a mixture of agricultural residues containing orange peels carried out by the fungal strains Aspergillus niger SKN1 and Trametes hirsuta SKH1 and subsequently valorization of the hydrolysate through fermentation with Clostridium acetobutylicum ATCC824 to produce biobutanol. Raw orange bagasse pellets were also subjected to fermentation with a Clostridium beijerinckii strain to produce butanol [103]. Citrus processing waste can be utilized by various Lactobacillus spp. to achieve lactic acid fermentation. Lactobacillus casei 2246 fermented orange peels through a yield of 0.88 g lactic acid/g d.w. under static cultivation [104]. Another example is L. delbrueckii subsp. delbrueckii, which could utilize the hydrolysate of orange peels to produce D-lactic acid [105]. Solid-state fermentation of orange peels can be achieved by Aspergillus spp., e.g., A. oryzae and A. niger bioconverted orange peels and sugarcane bagasse as well as orange peels to galacturonic acid [106] and citric acid [37], respectively. In addition, cultivation of the alga Euglena gracilis on orange peels resulted in β-glucan production [107].
The solid-state fermentation of orange peels and grape pomace by the fungus Aspergillus awamori was carried out by Díaz et al. [108] in both packed bed and tray-type bioreactors. They produced a fermentation product with high xylanolytic, cellulolytic and pectinolytic activity that was then applied effectively for orange juice clarification. Moreover, the pectinolytic, cellulolytic and xylanolytic potential of the fungi Aspergillus niger BTL, Fusarium oxysporum F3, Neurospora crassa DSM 1129 and a Penicillium decumbens sp. were evaluated under solid-state fermentation of orange peels, revealing that A. niger BTL exhibited the highest β-xylosidase, polygalacturonase, invertase and pectate lyase activity, whereas N. crassa DSM 1129 demonstrated the highest endoglucanase activity [109]. In addition, Tao et al. [110] performed solid-state fermentation of sweet orange processing waste using a Eupenicillium javanicum strain, reporting endoglucanase, β-glucosidase and pectinase activities of approximately 50 U/g and xylanase activity near 105 U/g. Solid-sate fermentation of orange peels using a Trichoderma viride strain resulted in high cellulolytic activity, exceeding 400 U/mL [111], while, using Aspergillus brasiliensis, led to polygalacturonase activity up to 45 U/g [112]. Cladosporium strains were also found to exhibit enhanced endoglucanase, exoglucanase, xylanase, pectinase and amylase activities during both submerged and solid-state fermentation of orange peels [113]. Solid-state fermentation of a mixture of orange peels and exhausted sugar beet cossettes caused the induction of high xylanase and exo-polygalacturonase activities, whereas addition of commercially available cellulases to the fermented material permitted the effective hydrolysis of this food waste [114]. Giese et al. [115] proceeded orange bagasse by the fungal strain Botryosphaeria rhodina MAMB-05 to produce a solid-state fermentation product with high pectinase activity. An α-amylase activity of 8.5 U/mL was recorded by Ben Hadj Hmida et al. [116] during treatment of orange peels with Bacillus cereus, whereas Ousaadi et al. [117] determined α-amylase activity of 12.19 U/mL by growing a halophilic Streptomyces strain in orange peel-derived medium. In addition, Serra et al. [118] achieved the heterologous expression of a polygalacturonase gene from the thermophile Thermomyces lanuginosus to the Komagataella phaffii yeast, recording recombinant pectinase activity up to 460 U/mL. Moreover, yeasts of Wickerhamomyces subpelliculosus could exhibit L-methioninase activity of 94.08 U/mL during orange pulp processing [119].

7. Bioactive Compounds and Antioxidant Properties of Raw and Biotreated Citrus Processing Waste

Citrus processing residues can be used as a source for the recovery of bioactive compounds (Table 6) that can be applied as dietary supplements in functional foods [120]. Essential oils, phenolics and pectin as well as cellulosic material can be obtained from orange peels through the implementation of a biorefinery approach [121]. Pulsed electric field of 7 kV/cm, which assists the extraction of bioactive compounds, led to increased recovery of naringin and hesperidin from orange residues, which possess high antioxidant capacity [122], while hesperidin from orange peels could biotransform to the antioxidant diosmetin [123]. Application of a recombinant α-L-rhamnosidase resulted in the hydrolysis of naringin to rhamnose [124], whereas enzymatic hydrolysis combined with ultrasonic treatment permitted the bioconversion of orange processing waste to β-carotene [125].
Apart from the production of hydrolytic enzymes for the food and beverage industry, citrus processing waste through biotreatment can serve as a potential source of recovering high value-added products for food applications, such as antioxidants. Bier et al. [126] evaluated the antioxidant activity of the solid-state fermentation product derived from the bioconversion of limonene present in orange processing waste after inoculation with a Diaporthe strain. Sepúlveda et al. [127] valorized the high polyphenolic content of orange processing waste to produce the antioxidant and antibacterial compound ellagic acid at a yield of 19 mg/g of dry orange peel through submerged fermentation. Yu et al. [128] also applied mixed-type fermentation of orange peel pomace using Lactobacillus casei, Aspergillus oryzae and Trichoderma koningii at a microbial species ratio of 7:5:1, resulting in increased antioxidant capacity of the fermented byproduct, with metabolomics analysis indicating the positive impact of biomolecules such as pinoresinol, gentisic acid, quercetin 3-galactoside 7-rhamnoside and quercetin 3-lathyroside. However, a key factor in the development of bioconversion strategies for citrus processing waste into high-value products is the standardization of the bioconversion process.

8. Citrus Processing Waste as a Source of Specialized Microbial Starter Cultures

Citrus processing waste is also considered a source for selecting microbial starting cultures. For instance, Zerva et al. [129] reported that spontaneous fermentation of orange processing waste led almost exclusively to the proliferation of lactic acid bacteria and yeasts with potential applications as starting inocula in food and environmental applications. Despite the broad diversity of indigenous microorganisms in citrus processing waste capable of degrading pectin, cellulose and hemicellulose, which are perfectly adapted to citrus residues environment, their application is restricted, and allochthonous microbial strains are often applied during solid-state fermentation [129,130,131]. Therefore, citrus processing waste is considered a valuable source for the isolation of pectin-, cellulose- and hemicellulose-degrading microorganisms or the recovery of specialized mixed cultures consisting of such indigenous microbiota, with potential uses in the food and beverage industry, like in must [132] and juice [130] clarification. Despite the broad diversity of these degrading microbiota in citrus processing waste, the application of indigenous microorganisms capable of degrading pectin, cellulose and hemicellulose, which their growth is perfectly adapted to citrus residues, is restricted, and allochthonous microbial strains are often applied during solid-state fermentation. Indeed, solid-state fermentation of citrus waste with autochthonous microbiota, either in pure or mixed cultures, appears to be advantageous for biotechnological applications in food and environmental technology, and in animal feeding.

9. Valorization of Citrus Processing Waste as a Sustainable Ingredient in Animal Feeding

Citrus processing waste can also be valorized in animal feeding by substituting common nutrient compounds in animal diets. For instance, orange processing waste was used as a substitute ingredient in fish diets, such as that of Labeo rohita, to replace basic dietary materials like wheat flour and rice bran [133]. Rego et al. [134] evaluated the effects of substituting corn with orange pulp in lamb diets and found that while lamb weight remained unchanged, increasing the proportion of orange pulp in the diet led to reduced fat deposition and muscle area. Researchers have also highlighted orange peels as a promising feed option for small ruminants like dairy ewes [135], which with proper processing, could serve as supplements to improve animal health and nutritional status [136]. Varela et al. [137] reported that rabbit diets with up to 30% orange pulp can be used as a substitute of conventional diets without affecting their digestibility. By using orange pulp as a dietary supplement of laying hens at 7% and 10%, Hussein et al. [138] found that a range of parameters, such as body weight gain, feed intake and feed conversion ratio, as well as egg production, weight and mass, were ameliorated compared to the control. Moreover, the use of orange pulp in the diet of the laying hens increased eggshell weight and thickness and intensified egg yolk color, resulting in a better antioxidant capacity and a more preferable fatty acid composition. However, in a study by Goliomytis et al. [139] where laying hens were dietary supplemented with 9% orange pulp, the improved egg yolk oxidative capacity observed was accompanied with deteriorated performance because of reduced feed intake, which was attributed to the reduced palatability of the citrus pulp. The differences in citrus pulp composition and constituents, such as the percentage of seeds that are rich in tannins and pectin and may affect palatability, may explain discrepancies among published studies. On the other hand, improved meat oxidative stability during refrigerated storage without any adverse effects on the performance of broiler chickens fed with a diet containing 5% citrus pulp [140] suggests that citrus pulp may successfully incorporate in broiler diets. Although citrus processing waste can be used in animal feed as stated, the lack of agronomic standardization may hinder its wider application [141].

10. Conclusions

Citrus processing waste is an abundant resource for the recovery of high value-added products, including antioxidants, hydrolytic enzymes and biodegradable packaging materials, and the synthesis of innovative adsorbent nanostructured material. Bioconversion of citrus residues like peels, seeds and pulp, following various biotreatment techniques, such as solid-state fermentation, which is not inhibited by their high content in essential oils, can result in the effective waste management of this agricultural byproduct, reducing environmental impact and resulting simultaneously to the formation of innovative functional compounds within the bioeconomy prism. Bioconverted citrus residues may result in enhanced soil fertility and phytoprotection, whereas citrus processing waste can comprise an alternative feedstuff in animal diets. Such biotreatment approaches can boost agri-food, pharmaceutical and energy sectors in citrus producing countries. Although the employment of the above-mentioned valorization bioengineering methods can boost the economy of local communities in citrus processing countries, issues like the variation in the composition of citrus residues and the type of fermentation method employed should be addressed. Moreover, the legislation framework dealing with the use of agro-industrial residues, including citrus processing waste, and their substrates as functional food and feed additives should be reconsidered and simplified. These biotechnological approaches should also be evaluated through detailed life cycle assessment and advanced techno-economic analyses to assess the feasibility of their implementation. Further research on optimizing the recovery of bioactive compounds and the fermentation process will facilitate the adoption of such sustainable technological solutions.

Author Contributions

Investigation, I.S. and S.N.; writing—original draft preparation, I.S. and S.N.; writing—review and editing, I.S., S.N., P.M., N.K., M.G. and P.S.; Conceptualization, I.S. and S.N.; project administration and supervision, S.N. All authors have read and agreed to the published version of the manuscript.

Funding

This work was conducted in the frame of the research project entitled “Multipurpose solid state fermentation as an integrated biorefinery approach to valorize orange processing waste for food and animal feed”, acronym “FERONIA”, which is implemented in the framework of H.F.R.I call “Basic research Financing (Horizontal support of all Sciences)” under the National Recovery and Resilience Plan “Greece 2.0” funded by the European Union—NextGenerationEU (H.F.R.I. Project Number: 014995).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

No new data were created or analyzed in this study. Data sharing is not applicable to this article.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Food and Agriculture Organization of the United Nations (FAO). FAOSTAT. Available online: https://www.fao.org/faostat/en/#data/QCL (accessed on 5 June 2025).
  2. Romelle, F.D.; Rani, A.; Manohar, R.S. Chemical composition of some selected fruit peels. Eur. J. Food Sci. Technol. 2016, 4, 12–21. [Google Scholar]
  3. Olabinjo, O.O.; Ogunlowo, A.S.; Ajayi, O.O.; Olalusi, A.P. Analysis of physical and chemical composition of sweet orange (Citrus sinensis) peels. Int. J. Environ. Agric. Biotechnol. 2017, 2, 2201–2206. [Google Scholar] [CrossRef]
  4. Jentzsch, M.; Badstöber, M.C.; Umlas, F.; Speck, T. Damage protection in fruits: Comparative analysis of the functional morphology of the fruit peels of five Citrus species via quasi-static compression tests. Front. Mater. 2022, 9, 979151. [Google Scholar] [CrossRef]
  5. Jentzsch, M.; Becker, S.; Thielen, M.; Speck, T. Functional anatomy, impact behavior and energy dissipation of the peel of Citrus limon: A comparison of Citrus limon and Citrus maxima. Plants 2022, 11, 991. [Google Scholar] [CrossRef]
  6. Ahmad, M.M.; Qureshi, T.M.; Nadeem, M.; Asghar, M. Variability in peel composition and quality evaluation of peel oils of citrus varieties. J. Agric. Res. 2016, 54, 747–756. [Google Scholar]
  7. Kumar, P.G.; Paul, S.K.; Khobragade, C.B.; Bania, B.K.; Sengupta, D.K. Requirements of mixed tangerine (Citrus tangerina) and pineapple (Ananas comosus) powdered peel wastes fermentation for citric acid production. Agric. Eng. Int. CIGR J. 2020, 22, 194–207. [Google Scholar]
  8. Patil, B.N.; Gupta, S.V.; Bharad, S.G.; Gahukar, S.J.; Patil, N.B. Physicochemical properties and mass modelling of Nagpur mandarin (Citrus reticulata) fruit. J. Pharm. Innov. 2021, 10, 1784–1791. [Google Scholar]
  9. Kalompatsios, D.; Palaiogiannis, D.; Makris, D.P. Optimized production of a hesperidin-enriched extract with enhanced antioxidant activity from waste orange peels using a glycerol/sodium butyrate deep eutectic solvent. Horticulturae 2024, 10, 208. [Google Scholar] [CrossRef]
  10. Kanaze, F.I.; Termentzi, A.; Gabrieli, C.; Niopas, I.; Georgarakis, M.; Kokkalou, E. The phytochemical analysis and antioxidant activity assessment of orange peel (Citrus sinensis) cultivated in Greece–Crete indicates a new commercial source of hesperidin. Biomed. Chromatogr. 2009, 23, 239–249. [Google Scholar] [CrossRef]
  11. Toprakçı, G.; Toprakçı, İ.; Şahin, S. Highly clean recovery of natural antioxidants from lemon peels: Lactic acid-based automatic solvent extraction. Phytochem. Anal. 2022, 33, 554–563. [Google Scholar] [CrossRef]
  12. Li, P.; Yao, X.; Zhou, Q.; Meng, X.; Zhou, T.; Gu, Q. Citrus peel flavonoid extracts: Health-beneficial bioactivities and regulation of intestinal microecology in vitro. Front. Nutr. 2022, 9, 888745. [Google Scholar] [CrossRef] [PubMed]
  13. da Cunha, C.T.; Oliveira, A.F.; Fernandes, V.B.; Mendes, F.N.P.; Vieira, Í.G.P. Development of a functional ingredient rich in hesperidin from citrus fruit wastes. Res. Soc. Dev. 2021, 10, e369101220530. [Google Scholar] [CrossRef]
  14. Castro-Vazquez, L.; Alañón, M.E.; Rodríguez-Robledo, V.; Pérez-Coello, M.S.; Hermosín-Gutierrez, I.; Díaz-Maroto, M.C.; Arroyo-Jimenez, M.D.M. Bioactive flavonoids, antioxidant behaviour, and cytoprotective effects of dried grapefruit peels (Citrus paradisi Macf.). Oxid. Med. Cell. Longev. 2016, 2016, 8915729. [Google Scholar] [CrossRef]
  15. Ngoc, T.N.T.; Van Hung, P.; Phi, N.T.L. Extraction of flavonoids in pomelos’ peels using Box-Behnken response surface design and their biological activities. Viet. J. Sci. Technol. Eng. 2021, 63, 52–57. [Google Scholar]
  16. Helmy, M.G.; Khalil, M.; Zein, R. Phenolics content, antioxidant, antibacterial and anticancer activities of pomelo peels. J. Microbiol. Biotechnol. Food Sci. 2025, e12039. [Google Scholar] [CrossRef]
  17. Karne, H.; Kelkar, V.; Mundhe, A.; Ikar, M.; Betawar, S.; Chaudhari, N. Essential oil extraction from orange and lemon peel. E3S Web Conf. 2023, 455, 01005. [Google Scholar] [CrossRef]
  18. Li, Z.; Ma, Y.; Hollmann, F.; Wang, Y. Study on green extraction of limonene from orange peel and cascade catalysis to produce carvol and carvone in deep eutectic solvents. Flavour Fragr. J. 2022, 37, 254–261. [Google Scholar] [CrossRef]
  19. El Aboubi, M.; Hdech, D.B.; Bikri, S.; Benayad, A.; El Magri, A.; Aboussaleh, Y.; Aouane, E.M. Chemical composition of essential oils of Citrus limon peel from three Moroccan regions and their antioxidant, anti-inflammatory, antidiabetic and dermatoprotective properties. J. Herbmed Pharmacol. 2022, 12, 118–127. [Google Scholar] [CrossRef]
  20. Himed, L.; Merniz, S.; Monteagudo-Olivan, R.; Barkat, M.; Coronas, J. Antioxidant activity of the essential oil of citrus limon before and after its encapsulation in amorphous SiO2. Sci. Afr. 2019, 6, e00181. [Google Scholar] [CrossRef]
  21. Okunowo, W.O.; Oyedeji, O.; Afolabi, L.O.; Matanmi, E. Essential oil of grape fruit (Citrus paradisi) peels and its antimicrobial activities. Am. J. Plant Sci. 2013, 4, 1–9. [Google Scholar] [CrossRef]
  22. Tran, T.H.; Dao, T.P.; Le, X.T.; Huynh, B.L.; Minh, L.T.N. Volatile compounds of grapefruit (Citrus Grandis (L.) Osbeck) peel essential oil by cold pressing and hydrodistillation methods. IOP Conf. Ser. Earth Environ. Sci. 2023, 1241, 012070. [Google Scholar] [CrossRef]
  23. Das, S.C.; Hossain, M.; Hossain, M.Z.; Jahan, N.; Uddin, M.A. Chemical analysis of essential oil extracted from pomelo sourced from Bangladesh. Heliyon 2022, 8, e12137. [Google Scholar] [CrossRef]
  24. Sirisomboon, P.; Duangchang, J.; Phanomsophon, T.; Lapcharoensuk, R.; Shrestha, B.P.; Kasemsamran, S.; Tsuchikawa, S. Analysis of the pomelo peel essential oils at different storage durations using a visible and near-infrared spectroscopic on intact fruit. Foods 2024, 13, 2379. [Google Scholar] [CrossRef] [PubMed]
  25. Dao, T.P.; Ngo, T.C.Q.; Le, T.D.; Ngo, H.D.; Thao, P.; Tran, T.G.; Huynh, X.P. Comparative study of mandarin (Citrus reticulata Blanco) essential oil extracted by microwave-assisted hydrodistillation, microwave extraction and hydrodistillation methods. IOP Conf. Ser. Mater. Sci. Eng. 2020, 991, 012129. [Google Scholar] [CrossRef]
  26. Meryem, S.; Mohamed, D.; Nour-Eddine, C.; Faouzi, E. Chemical composition, antibacterial and antioxidant properties of three Moroccan citrus peel essential oils. Sci. Afr. 2023, 20, e01592. [Google Scholar] [CrossRef]
  27. Fakayode, O.A.; Abobi, K.E. Optimization of oil and pectin extraction from orange (Citrus sinensis) peels: A response surface approach. J. Anal. Sci. Technol. 2018, 9, 1–16. [Google Scholar] [CrossRef]
  28. Kamal, M.M.; Kumar, J.; Mamun, M.A.H.; Ahmed, M.N.U.; Shishir, M.R.I.; Mondal, S.C. Extraction and characterization of pectin from Citrus sinensis peel. J. Biosyst. Eng. 2021, 46, 16–25. [Google Scholar] [CrossRef]
  29. Pei, C.C.; Hsien, T.S.; Hsuan, F.C.; Hsuan, H.L.; Chi, C.C.; Yi, L.M. Microwave- and ultrasound-assisted extraction of pectin yield and physicochemical properties from lemon peel. J. Agric. Food Res. 2024, 15, 101009. [Google Scholar] [CrossRef]
  30. Salma, M.A.; Jahan, N.; Islam, M.A.; Hoque, M.M. Extraction of pectin from lemon peel: Technology development. J. Chem. Eng. 2012, 27, 25–30. [Google Scholar] [CrossRef]
  31. Mohamed, H. Extraction and characterization of pectin from grapefruit peels. MOJ Food Process. Technol. 2016, 2, 31–38. [Google Scholar] [CrossRef]
  32. Wang, W.; Ma, X.; Xu, Y.; Cao, Y.; Jiang, Z.; Ding, T.; Liu, D. Ultrasound-assisted heating extraction of pectin from grapefruit peel: Optimization and comparison with the conventional method. Food Chem. 2015, 178, 106–114. [Google Scholar] [CrossRef]
  33. Pagarra, H.; Rachmawaty, R.; Sahribulan, S. Optimization of pectin extraction from pomelo peels (Citrus maxima) using response surface methodology. Bionature 2024, 25, 28–36. [Google Scholar] [CrossRef]
  34. Quoc, L.P.T. Effect of the assistance of microwave and oxalic acid on the extraction yield of pectin from pomelo (Citrus maxima) peel. Bulg. J. Agric. Sci. 2019, 25, 192–196. [Google Scholar]
  35. Colodel, C.; Vriesmann, L.C.; Teófilo, R.F.; de Oliveira Petkowicz, C.L. Extraction of pectin from Ponkan (Citrus reticulata Blanco cv. Ponkan) peel: Optimization and structural characterization. Int. J. Biol. Macromol. 2018, 117, 385–391. [Google Scholar] [CrossRef]
  36. Twinomuhwezi, H.; Godswill, A.C.; Kahunde, D. Extraction and characterization of pectin from orange (Citrus sinensis), lemon (Citrus limon) and tangerine (Citrus tangerina). Am. J. Phys. Sci. 2020, 1, 17–30. [Google Scholar] [CrossRef]
  37. Rivas, B.; Torrado, A.; Torre, P.; Converti, A.; Domínguez, J.M. Submerged citric acid fermentation on orange peel autohydrolysate. J. Agric. Food Chem. 2008, 56, 2380–2387. [Google Scholar] [CrossRef]
  38. Orozco, R.S.; Hernández, P.B.; Morales, G.R.; Núñez, F.U.; Villafuerte, J.O.; Lugo, V.L.; Vázquez, P.C. Characterization of lignocellulosic fruit waste as an alternative feedstock for bioethanol production. BioResources 2014, 9, 1873–1885. [Google Scholar] [CrossRef]
  39. Núñez-Gómez, V.; San Mateo, M.; González-Barrio, R.; Periago, M.J. Chemical composition, functional and antioxidant properties of dietary fibre extracted from lemon peel after enzymatic treatment. Molecules 2024, 29, 269. [Google Scholar] [CrossRef] [PubMed]
  40. Ververis, C.; Georghiou, K.; Danielidis, D.; Hatzinikolaou, D.G.; Santas, P.; Santas, R.; Corleti, V. Cellulose, hemicelluloses, lignin and ash content of some organic materials and their suitability for use as paper pulp supplements. Bioresour. Technol. 2007, 98, 296–301. [Google Scholar] [CrossRef]
  41. Rivas-Cantu, R.C.; Jones, K.D.; Mills, P.L. A citrus waste-based biorefinery as a source of renewable energy: Technical advances and analysis of engineering challenges. Waste Manag. Res. 2013, 31, 413–420. [Google Scholar] [CrossRef] [PubMed]
  42. Nor Fazelin, M.Z.; Salma Mohamad Yusop, S.M.Y.; Ishak Ahmad, I.A. Preparation and characterization of cellulose and nanocellulose from pomelo (Citrus grandis) albedo. J. Nutr. Food Sci. 2015, 5, 334. [Google Scholar]
  43. Wang, H.; Wang, P.; Kasapis, S.; Truong, T. Pomelo (Citrus grandis L.) peels as effective sorbents for diverse gel matrices: The influence of particle size and powder concentration. J. Food Eng. 2024, 370, 111966. [Google Scholar] [CrossRef]
  44. Boluda-Aguilar, M.; García-Vidal, L.; González-Castañeda, F.P.; López-Gómez, A. Mandarin peel wastes pretreatment with steam explosion for bioethanol production. Bioresour. Technol. 2010, 101, 3506–3513. [Google Scholar] [CrossRef]
  45. Prajapati, P.; Porwal, C.; Garg, M.; Singh, N.; Sadhu, S.D.; Chopra, R.; Tripathi, A.D. Transforming lemon peel into a sustainable reservoir of bioactives: A green osmotic dehydration strategy. Food Chem. X 2025, 25, 102172. [Google Scholar] [CrossRef]
  46. Umaña, M.; Simal, S.; Dalmau, E.; Turchiuli, C.; Chevigny, C. Evaluation of different pectic materials coming from citrus residues in the production of films. Foods 2024, 13, 2138. [Google Scholar] [CrossRef] [PubMed]
  47. Yun, D.; Liu, J. Preparation, characterization and application of active food packaging films based on sodium alginate and twelve varieties of mandarin peel powder. Foods 2024, 13, 1174. [Google Scholar] [CrossRef]
  48. Nithish, S.; Kumar, R.P.; Rawat, L.K.; Afzia, N.; Ghosh, T. Extraction of pectin from Assam lemon (Citrus limon) peel and its use in preparation of low-fat mayonnaise. Sustain. Food Technol. 2025, 3, 1128–1135. [Google Scholar]
  49. Mahato, N.; Sinha, M.; Sharma, K.; Koteswararao, R.; Cho, M.H. Modern extraction and purification techniques for obtaining high purity food-grade bioactive compounds and value-added co-products from citrus wastes. Foods 2019, 8, 523. [Google Scholar] [CrossRef]
  50. Mvumi, B.M.; Gwenzi, W.; Mhandu, M.G. Ecotoxicological effects of citrus processing waste on earthworms, Lumbricus terrestris L. Ind. Crops Prod. 2017, 110, 123–129. [Google Scholar] [CrossRef]
  51. Andiloro, S.; Calabrò, P.S.; Folino, A.; Zema, D.A.; Zimbone, S.M. Evaluating the pollution risk of soil due to natural drainage of orange peel: First results. Environments 2021, 8, 43. [Google Scholar] [CrossRef]
  52. Karunya, S.K.; Saranraj, P. Toxic effects of pesticide pollution and its biological control by microorganisms: A review. Appl. J. Hyg. 2014, 3, 01–10. [Google Scholar]
  53. Hollins, O.; Lee, P.; Sims, E.; Bertham, O.; Symington, H.; Bell, N.; Pfaltzgraff, L.; Sjögren, P. Towards a Circular Economy—Waste Management in the EU. Study, Science and Technology Options Assessment; PE 581.913; European Parliamentary Research Service (EPRS), Scientific Foresight Unit (STOA): Brussels, Belgium, 2017. [Google Scholar]
  54. A new Circular Economy Action Plan—For a cleaner and more competitive Europe. In Communication from the Commission to the European Parliament, the Council, the European Economic and Social Committee and the Committee of the Regions; COM(2020) 98 Final; European Commission: Brussels, Belgium, 2020; Available online: https://eur-lex.europa.eu/legal-content/EN/TXT/HTML/?uri=CELEX:52020DC0098 (accessed on 5 June 2025).
  55. Regulation (EU) 2019/1009 of the European Parliament and of the Council of 5 June 2019 Laying Down Rules on the Making Available on The market of EU Fertilising Products and Amending Regulations (EC) No 1069/2009 and (EC) No 1107/2009 and Repealing Regulation (EC) No 2003/2003 (Text with EEA Relevance). Available online: http://data.europa.eu/eli/reg/2019/1009/oj (accessed on 5 June 2025).
  56. Regulation (EC) No 1069/2009 of the European Parliament and of the Council of 21 October 2009 Laying Down Health Rules as Regards Animal By-Products and Derived Products Not Intended for Human Consumption and Repealing Regulation (EC) No 1774/2002 (Animal by-Products Regulation). Available online: http://data.europa.eu/eli/reg/2009/1069/oj (accessed on 5 June 2025).
  57. Rao, M.; Bilić, L.; Bast, A.; de Boer, A. What does it take to close the loop? Lessons from a successful citrus waste valorisation business. Br. Food J. 2024, 126, 143–161. [Google Scholar] [CrossRef]
  58. Wikandari, R.; Millati, R.; Cahyanto, M.N.; Taherzadeh, M.J. Biogas production from citrus waste by membrane bioreactor. Membranes 2014, 4, 596–607. [Google Scholar] [CrossRef] [PubMed]
  59. Zema, D.A.; Fòlino, A.; Zappia, G.; Calabrò, P.S.; Tamburino, V.; Zimbone, S.M. Anaerobic digestion of orange peel in a semi-continuous pilot plant: An environmentally sound way of citrus waste management in agro-ecosystems. Sci. Total Environ. 2018, 630, 401–408. [Google Scholar] [CrossRef]
  60. Carvalho, A.; Fragoso, R.; Gominho, J.; Duarte, E. Effect of minimizing d-limonene compound on anaerobic co-digestion feeding mixtures to improve methane yield. Waste Biomass Valorization 2019, 10, 75–83. [Google Scholar] [CrossRef]
  61. Jimenez-Castro, M.P.; Buller, L.S.; Zoffreo, A.; Timko, M.T.; Forster-Carneiro, T. Two-stage anaerobic digestion of orange peel without pre-treatment: Experimental evaluation and application to São Paulo state. J. Environ. Chem. Eng. 2020, 8, 104035. [Google Scholar] [CrossRef]
  62. Torquato, L.D.; Pachiega, R.; Crespi, M.S.; Nespeca, M.G.; de Oliveira, J.E.; Maintinguer, S.I. Potential of biohydrogen production from effluents of citrus processing industry using anaerobic bacteria from sewage sludge. Waste Manag. 2017, 59, 181–193. [Google Scholar] [CrossRef]
  63. Camargo, F.P.; Sakamoto, I.K.; Bize, A.; Duarte, I.C.S.; Silva, E.L.; Varesche, M.B.A. Screening design of nutritional and physicochemical parameters on bio-hydrogen and volatile fatty acids production from citrus peel waste in batch reactors. Int. J. Hydrogen Energy 2021, 46, 7794–7809. [Google Scholar] [CrossRef]
  64. Saadatinavaz, F.; Karimi, K.; Denayer, J.F. Hydrothermal pretreatment: An efficient process for improvement of biobutanol, biohydrogen, and biogas production from orange waste via a biorefinery approach. Bioresour. Technol. 2021, 341, 125834. [Google Scholar] [CrossRef] [PubMed]
  65. Choi, I.S.; Lee, Y.G.; Khanal, S.K.; Park, B.J.; Bae, H.J. A low-energy, cost-effective approach to fruit and citrus peel waste processing for bioethanol production. Appl. Energy 2015, 140, 65–74. [Google Scholar] [CrossRef]
  66. Plessas, S.; Bekatorou, A.; Koutinas, A.A.; Soupioni, M.; Banat, I.M.; Marchant, R. Use of Saccharomyces cerevisiae cells immobilized on orange peel as biocatalyst for alcoholic fermentation. Bioresour. Technol. 2007, 98, 860–865. [Google Scholar] [CrossRef]
  67. Carota, E.; Petruccioli, M.; D’Annibale, A.; Gallo, A.M.; Crognale, S. Orange peel waste–based liquid medium for biodiesel production by oleaginous yeasts. Appl. Microbiol. Biotechnol. 2020, 104, 4617–4628. [Google Scholar] [CrossRef] [PubMed]
  68. Matouk, A.M.; Abu-Elreesh, G.M.; Abdel-Rahman, M.A.; Desouky, S.E.; Hashem, A.H. Response surface methodology and repeated-batch fermentation strategies for enhancing lipid production from marine oleaginous Candida parapsilosis Y19 using orange peel waste. Microb. Cell Factories 2025, 24, 16. [Google Scholar] [CrossRef] [PubMed]
  69. Moser, B.R.; Dorado, C.; Bantchev, G.B.; Winkler-Moser, J.K.; Doll, K.M. Production and evaluation of biodiesel from sweet orange (Citrus sinensis) lipids extracted from waste seeds from the commercial orange juicing process. Fuel 2023, 342, 127727. [Google Scholar] [CrossRef]
  70. Fazzino, F.; Mauriello, F.; Paone, E.; Sidari, R.; Calabrò, P.S. Integral valorization of orange peel waste through optimized ensiling: Lactic acid and bioethanol production. Chemosphere 2021, 271, 129602. [Google Scholar] [CrossRef]
  71. Calabrò, P.S.; Fazzino, F.; Sidari, R.; Zema, D.A. Optimization of orange peel waste ensiling for sustainable anaerobic digestion. Renew. Energy 2020, 154, 849–862. [Google Scholar] [CrossRef]
  72. Consoli, S.; Caggia, C.; Russo, N.; Randazzo, C.L.; Continella, A.; Modica, G.; Cacciola, S.O.; Faino, L.; Reverberi, M.; Baglieri, A.; et al. Sustainable use of citrus waste as organic amendment in orange orchards. Sustainability 2023, 15, 2482. [Google Scholar] [CrossRef]
  73. Kato-Noguchi, H.; Kato, M. Pesticidal activity of citrus fruits for the development of sustainable fruit-processing waste management and agricultural production. Plants 2025, 14, 754. [Google Scholar] [CrossRef] [PubMed]
  74. Van Heerden, I.; Cronjé, C.; Swart, S.H.; Kotzé, J.M. Microbial, chemical and physical aspects of citrus waste composting. Bioresour. Technol. 2002, 81, 71–76. [Google Scholar] [CrossRef]
  75. De Medina-Salas, L.; Giraldi-Díaz, M.R.; Castillo-González, E.; Morales-Mendoza, L.E. Valorization of orange peel waste using precomposting and vermicomposting processes. Sustainability 2020, 12, 7626. [Google Scholar] [CrossRef]
  76. Sorgonà, A.; Abenavoli, M.R.; Cacco, G.; Gelsomino, A. Growth of tomato and zucchini seedlings in orange waste compost media: pH and implication of dosage. Compost Sci. Util. 2011, 19, 189–196. [Google Scholar] [CrossRef]
  77. Tuttobene, R.; Avola, G.; Gresta, F.; Abbate, V. Industrial orange waste as organic fertilizer in durum wheat. Agron. Sustain. Dev. 2009, 29, 557–563. [Google Scholar] [CrossRef]
  78. Shehata, S.A.; El-Metwally, I.M.; Abdelgawad, K.F.; Elkhawaga, F.A. Efficacy of agro-industrial wastes on the weed control, nutrient uptake, growth, and yield of onion crop (Allium cepa L.). J. Soil Sci. Plant Nutr. 2022, 22, 2707–2718. [Google Scholar] [CrossRef]
  79. Ugolini, F.; Crisci, A.; Baronti, S.; Cencetti, G.; Dal Prà, A.; Albanese, L.; Michelozzi, M.; Zabini, F.; Meneguzzo, F. Effects of orange waste extract produced by hydrodynamic cavitation on the germination of Chenopodium album L. and Lactuca sativa L. Sustainability 2024, 16, 3039. [Google Scholar] [CrossRef]
  80. Hussain, O.A.; Rahim, E.A.A.; Badr, A.N.; Hathout, A.S.; Rashed, M.M.; Fouzy, A.S. Total phenolics, flavonoids, and antioxidant activity of agricultural wastes, and their ability to remove some pesticide residues. Toxicol. Rep. 2022, 9, 628–635. [Google Scholar] [CrossRef]
  81. El Kasimi, R.; Douiri, F.; Haddi, K.; Boughdad, A. Bioactivity of essential oil from Citrus aurantium peel against the pulse beetle Callosbruchus maculatus F. on chickpea. Agriculture 2023, 13, 232. [Google Scholar] [CrossRef]
  82. Duong, C.T.; Thao, H.T.P.; Tien, D.T.K.; Nga, N.T.T.; Nhan, T.C.; Huong, B.T.C.; Ercisli, S.; Truc, N.T.N.; Danh, L.T. Application of essential oils extracted from peel wastes of four orange varieties to control anthracnose caused by Colletotrichum scovillei and Colletotrichum gloeosporioides on mangoes. Plants 2023, 12, 2761. [Google Scholar] [CrossRef] [PubMed]
  83. Sala, A.; Vittone, S.; Barrena, R.; Sánchez, A.; Artola, A. Scanning agro-industrial wastes as substrates for fungal biopesticide production: Use of Beauveria bassiana and Trichoderma harzianum in solid-state fermentation. J. Environ. Manag. 2021, 295, 113113. [Google Scholar] [CrossRef]
  84. Suri, S.; Singh, A.; Nema, P.K. Current applications of citrus fruit processing waste: A scientific outlook. Appl. Food Res. 2022, 2, 100050. [Google Scholar] [CrossRef]
  85. Ríos Sosa, A.; Prado Barragán, L.A.; Ríos Reyes, A.; Aréchiga Carvajal, E.T. Genomic analysis and potential polyhydroxybutyrate (PHB) production from Bacillus strains isolated from extreme environments in Mexico. BMC Microbiol. 2025, 25, 15. [Google Scholar] [CrossRef]
  86. Gouda, M.; Abd El-Lateef, H.M.; Abou Taleb, M.F.; Abdelaziz, M.A.; Khalaf, M.M. Insight into the physicochemical characterization of composite orange peel fabricated packaging film: Fighting foodborne pathogens and oxidative stress. Int. J. Biol. Macromol. 2025, 306, 141777. [Google Scholar] [CrossRef]
  87. Pagliarini, E.; Minichiello, C.; Sisti, L.; Totaro, G.; Baffoni, L.; Di Gioia, D.; Saccani, A. From food waste to eco-friendly functionalized polymer composites: Investigation of orange peels as active filler. New Biotechnol. 2024, 80, 37–45. [Google Scholar] [CrossRef] [PubMed]
  88. Bertolo, M.R.; Pereira, T.S.; Dos Santos, F.V.; Facure, M.H.; Dos Santos, F.; Teodoro, K.B.R.; Mercante, L.A.; Correa, D.S. Citrus wastes as sustainable materials for active and intelligent food packaging: Current advances. Compr. Rev. Food Sci. Food Saf. 2025, 24, e70144. [Google Scholar] [CrossRef]
  89. Iffath, R.; Ara, R.; Ahmed, T.; Biswas, A. Fabrication and characterization of waste eggshell microparticles reinforced biodegradable composite packaging films enriched with pectin and orange peel essential oil. Appl. Food Res. 2025, 5, 100735. [Google Scholar] [CrossRef]
  90. Rastogi, S.; Tiwari, S.; Ratna, S.; Kumar, R. Utilization of agro-industrial waste for biosurfactant production under submerged fermentation and its synergistic application in biosorption of Pb2+. Bioresour. Technol. Rep. 2021, 15, 100706. [Google Scholar] [CrossRef]
  91. Kifle, D.; Bacha, K.; Gonfa, G. Antimicrobial activities of biosynthesized nanosilver using Musa paradisiaca and Citrus sinensis peel extracts against major human and plant pathogens. Sci. Rep. 2025, 15, 6600. [Google Scholar] [CrossRef]
  92. Desouky, M.M.; Abou-Saleh, R.H.; Moussa, T.A.; Fahmy, H.M. Nano-chitosan-coated, green-synthesized selenium nanoparticles as a novel antifungal agent against Sclerotinia sclerotiorum: In vitro study. Sci. Rep. 2025, 15, 1004. [Google Scholar] [CrossRef]
  93. Neisan, R.S.; Saady, N.M.C.; Bazan, C.; Zendehboudi, S. Optimization of arsenic removal from water using novel renewable adsorbents derived from orange peels. Waste Manag. Bull. 2025, 3, 21–35. [Google Scholar] [CrossRef]
  94. Kukowska, S.; Nowicki, P.; Szewczuk-Karpisz, K. New fruit waste-derived activated carbons of high adsorption performance towards metal, metalloid, and polymer species in multicomponent systems. Sci. Rep. 2025, 15, 1082. [Google Scholar] [CrossRef]
  95. Bouchelkia, N.; Tahraoui, H.; Benazouz, K.; Mameri, A.; Boudraa, R.; Moussa, H.; Hamri, N.; Merdoud, R.; Belkacemi, H.; Zoukel, A.; et al. Optimizing adsorption efficiency: A novel application of SVM_Boosting_IGWO for methylene blue dye removal using low-cost fruit peels adsorbents. Chemom. Intell. Lab. Syst. 2025, 261, 105377. [Google Scholar] [CrossRef]
  96. Balu, A.M.; Budarin, V.; Shuttleworth, P.S.; Pfaltzgraff, L.A.; Waldron, K.; Luque, R.; Clark, J.H. Valorisation of orange peel residues: Waste to biochemicals and nanoporous materials. ChemSusChem 2012, 5, 1694. [Google Scholar] [CrossRef]
  97. Abdelrazek, E.J.; Gahlan, A.A.; Gouda, G.A.; Ahmed, A.S. Cost-effective adsorption of cationic dyes using ZnO nanorods supported by orange peel-derived carbon. Sci. Rep. 2025, 15, 4123. [Google Scholar] [CrossRef]
  98. Schmidt, M.P.; Rupp, S.; Ashworth, D.J.; Phan, D.; Bhattacharjee, A.; Ferreira, J.F.S.; Men, Y.; Ibekwe, A.M. Feedstock selection influences performance and mechanism of DNA adsorption onto biochar. Environ. Nanotechnol. Monit. Manag. 2025, 23, 101040. [Google Scholar] [CrossRef]
  99. Wangchuk, S.; Promsuwan, K.; Saichanapan, J.; Soleh, A.; Saisahas, K.; Samoson, K.; Numnuam, A.; Kanatharana, P.; Thavarungkul, P.; Limbut, W. Cuprous oxide-functionalized activated porous carbon-modified screen-printed carbon electrode integrated with a smartphone for portable electrochemical nitrate detection. Talanta 2025, 287, 127581. [Google Scholar] [CrossRef] [PubMed]
  100. Singh, P.P.; Nath, G. Ultrasonic processing and thermo-acoustic analysis of orange peel waste as smart acoustic material: Waste and biomass valorization. Waste Biomass Valorization 2022, 13, 2905–2916. [Google Scholar] [CrossRef]
  101. Mihalyi, S.; Putz, A.; Draxler, M.; Mautner, A.; Sumetzberger-Hasinger, M.; Fabbri, F.; Pellis, A.; Neureiter, M.; Quartinello, F.; Guebitz, G.M. The orange gold: Biotechnological production of PLA/P(3HB)/limonene based polyesters from orange peel waste. Sustain. Mater. Technol. 2024, 41, e01110. [Google Scholar] [CrossRef]
  102. Mondal, S.; Santra, S.; Rakshit, S.; Halder, S.K.; Hossain, M.; Mondal, K.C. Saccharification of lignocellulosic biomass using an enzymatic cocktail of fungal origin and successive production of butanol by Clostridium acetobutylicum. Bioresour. Technol. 2022, 343, 126093. [Google Scholar] [CrossRef] [PubMed]
  103. da Silva, G.F.; Mathias, S.L.; de Menezes, A.J.; Vicente, J.G.P.; Delforno, T.P.; Varesche, M.B.A.; Duarte, I.C.S. Orange bagasse pellets as a carbon source for biobutanol production. Curr. Microbiol. 2020, 77, 4053–4062. [Google Scholar] [CrossRef]
  104. Ricci, A.; Diaz, A.B.; Caro, I.; Bernini, V.; Galaverna, G.; Lazzi, C.; Blandino, A. Orange peels: From by-product to resource through lactic acid fermentation. J. Sci. Food Agric. 2019, 99, 6761–6767. [Google Scholar] [CrossRef]
  105. De la Torre, I.D.; Acedos, M.G.; Ladero, M.; Santos, V.E. On the use of resting L. delbrueckii spp. delbrueckii cells for D-lactic acid production from orange peel wastes hydrolysates. Biochem. Eng. J. 2019, 145, 162–169. [Google Scholar] [CrossRef]
  106. Leh, D.S.; Biz, A.; De Paula, D.H.F.; Richard, P.; Gonçalves, A.G.; Noseda, M.D.; Mitchell, D.A.; Krieger, N. Conversion of citric pectin into D-galacturonic acid with high substrate loading using a fermented solid with pectinolytic activity. Biocatal. Agric. Biotechnol. 2017, 11, 214–219. [Google Scholar] [CrossRef]
  107. Yu, J.; Fang, L.; Kim, S.; Kim, K.; Kim, M.; Lee, T. Valorization of fruit and vegetable byproducts for the beta-glucan production from Euglena gracilis. Bioresour. Technol. 2024, 394, 130213. [Google Scholar] [CrossRef]
  108. Díaz, A.B.; Alvarado, O.; De Ory, I.; Caro, I.; Blandino, A. Valorization of grape pomace and orange peels: Improved production of hydrolytic enzymes for the clarification of orange juice. Food Bioprod. Process. 2013, 91, 580–586. [Google Scholar] [CrossRef]
  109. Mamma, D.; Kourtoglou, E.; Christakopoulos, P. Fungal multienzyme production on industrial by-products of the citrus-processing industry. Bioresour. Technol. 2008, 99, 2373–2383. [Google Scholar] [CrossRef] [PubMed]
  110. Tao, N.G.; Shi, W.Q.; Liu, Y.J.; Huang, S.R. Production of feed enzymes from citrus processing waste by solid-state fermentation with Eupenicillium javanicum. Int. J. Food Sci. Technol. 2011, 46, 1073–1079. [Google Scholar] [CrossRef]
  111. Irshad, M.; Anwar, Z.; But, H.I.; Afroz, A.; Ikram, N.; Rashid, U. The industrial applicability of purified cellulase complex indigenously produced by Trichoderma viride through solid-state bio-processing of agro-industrial and municipal paper wastes. BioResources 2013, 8, 145–157. [Google Scholar] [CrossRef]
  112. Laswai, F.C.; Matofari, J.W.; Nduko, J.M. Pectinolytic enzyme production from orange processing waste using Aspergillus brasiliensis strain. Biomass Conver. Biorefin. 2024, 14, 25173–25186. [Google Scholar] [CrossRef]
  113. Moharram, A.M.; Zohri, A.N.A.; Hesham, A.E.L.; Maher, M.A.A.; Shaban Al-Bedak, O.A.H.M. Production of cocktail enzymes by three Cladosporium isolates and bioconversion of orange peel wastes into valuable enzymes. J. Pure Appl. Microbiol. 2021, 15, 2336–2346. [Google Scholar] [CrossRef]
  114. Marzo, C.; Díaz, A.B.; Caro, I.; Blandino, A. Valorization of agro-industrial wastes to produce hydrolytic enzymes by fungal solid-state fermentation. Waste Manag. Res. 2019, 37, 149–156. [Google Scholar] [CrossRef]
  115. Giese, E.C.; Dekker, R.F.; Barbosa, A.M. Orange bagasse as substrate for the production of pectinase and laccase by Botryosphaeria rhodina MAMB-05 in submerged and solid state fermentation. BioResources 2008, 3, 335–345. [Google Scholar] [CrossRef]
  116. Ben Hadj Hmida, B.; Ben Mabrouk, S.; Fendri, A.; Hmida-Sayari, A.; Sayari, A. Optimization of newly isolated Bacillus cereus α-amylase production using orange peels and crab shells and application in wastewater treatment. 3 Biotech 2024, 14, 119. [Google Scholar] [CrossRef]
  117. Ousaadi, M.I.; Merouane, F.; Berkani, M.; Almomani, F.; Vasseghian, Y.; Kitouni, M. Valorization and optimization of agro-industrial orange waste for the production of enzyme by halophilic Streptomyces sp. Environ. Res. 2021, 201, 111494. [Google Scholar] [CrossRef]
  118. Serra, L.A.; Mendes, T.D.; De Marco, J.L.; de Almeida, J.R.M. Application of Thermomyces lanuginosus polygalacturonase produced in Komagataella phaffii in biomass hydrolysis and textile bioscouring. Enzyme Microb. Technol. 2024, 177, 110424. [Google Scholar] [CrossRef]
  119. Hassabo, A.A.; Mostafa, E.E.; Saad, M.M.; Selim, M.H. Utilization of orange pulp and corn steep liquor for L-methioninase production by Wickerhamomyces subpelliculosus. Egypt. Pharm. J. 2021, 20, 8–16. [Google Scholar] [CrossRef]
  120. Fathy, H.M.; Abd El-Maksoud, A.A.; Cheng, W.; Elshaghabee, F.M. Value-added utilization of citrus peels in improving functional properties and probiotic viability of Acidophilus-bifidus-thermophilus (ABT)-type synbiotic yoghurt during cold storage. Foods 2022, 11, 2677. [Google Scholar] [CrossRef]
  121. Tsouko, E.; Maina, S.; Ladakis, D.; Kookos, I.K.; Koutinas, A. Integrated biorefinery development for the extraction of value-added components and bacterial cellulose production from orange peel waste streams. Renew. Energy 2020, 160, 944–954. [Google Scholar] [CrossRef]
  122. Luengo, E.; Álvarez, I.; Raso, J. Improving the pressing extraction of polyphenols of orange peel by pulsed electric fields. Innov. Food Sci. Emerg. Technol. 2013, 17, 79–84. [Google Scholar] [CrossRef]
  123. Victor, M.M.; David, J.M.; Cortez, M.V.; Leite, J.L.; da Silva, G.S. A high-yield process for extraction of hesperidin from orange (Citrus sinensis L. osbeck) peels waste, and its transformation to diosmetin, a valuable and bioactive flavonoid. Waste Biomass Valorization 2021, 12, 313–320. [Google Scholar] [CrossRef]
  124. Kaur, A.; Singh, S.; Singh, R.S.; Schwarz, W.H.; Puri, M. Hydrolysis of citrus peel naringin by recombinant α-L-rhamnosidase from Clostridium stercorarium. J. Chem. Technol. Biotechnol. 2010, 85, 1419–1422. [Google Scholar] [CrossRef]
  125. Shahram, H.; Dinani, S.T. Optimization of ultrasonic-assisted enzymatic extraction of β-carotene from orange processing waste. J. Food Process Eng. 2019, 42, e13042. [Google Scholar] [CrossRef]
  126. Bier, M.C.J.; Medeiros, A.B.P.; De Kimpe, N.; Soccol, C.R. Evaluation of antioxidant activity of the fermented product from the biotransformation of R-(+)-limonene in solid-state fermentation of orange waste by Diaporthe sp. Biotechnol. Res. Innov. 2019, 3, 168–176. [Google Scholar] [CrossRef]
  127. Sepúlveda, L.; Laredo-Alcalá, E.; Buenrostro-Figueroa, J.J.; Ascacio-Valdés, J.A.; Genisheva, Z.; Aguilar, C.; Teixeira, J. Ellagic acid production using polyphenols from orange peel waste by submerged fermentation. Electron. J. Biotechnol. 2020, 43, 1–7. [Google Scholar] [CrossRef]
  128. Yu, H.; Xu, X.; Hao, J.; Zuo, X.; Wang, J.; Zhu, L.; Chen, M.; Lyu, Y.; Yan, Z.; Shen, Y.; et al. Mixed fermentation of citrus peel pomace with Trichoderma koningii, Aspergillus oryzae and Lactobacillus casei: Process optimization, antioxidant activities and non-targeted metabolomics analysis. Food Biosci. 2025, 66, 106180. [Google Scholar] [CrossRef]
  129. Zerva, I.; Remmas, N.; Ntougias, S. Diversity and biotechnological potential of xylan-degrading microorganisms from orange juice processing waste. Water 2019, 11, 274. [Google Scholar] [CrossRef]
  130. Zerva, I.; Remmas, N.; Ntougias, S. Biocatalyst potential of cellulose-degrading microorganisms isolated from orange juice processing waste. Beverages 2019, 5, 21. [Google Scholar] [CrossRef]
  131. Zerva, I.; Remmas, N.; Melidis, P.; Tsiamis, G.; Ntougias, S. Microbial succession and identification of effective indigenous pectinolytic yeasts from orange juice processing wastewater. Waste Biomass Valorization 2021, 12, 4885–4899. [Google Scholar] [CrossRef]
  132. Díaz, A.B.; Bolívar, J.; De Ory, I.; Caro, I.; Blandino, A. Applicability of enzymatic extracts obtained by solid state fermentation on grape pomace and orange peels mixtures in must clarification. LWT-Food Sci. Technol. 2011, 44, 840–846. [Google Scholar] [CrossRef]
  133. Deka, A.; Sahu, N.P.; Jain, K.K. Utilization of fruit processing wastes in the diet of Labeo rohita fingerling. Asian-Australas. J. Anim. Sci. 2003, 16, 1661–1665. [Google Scholar] [CrossRef]
  134. Rego, F.C.D.A.; Lima, L.D.D.; Baise, J.; Gasparini, M.J.; Eleodoro, J.I.; Santos, M.D.D.; Zundt, M. Performance, carcass and meat characteristics of lambs in feedlot fed diets with increasing levels of fresh orange pulp replacing corn. Ciênc. Anim. Bras. 2019, 20, e50129. [Google Scholar] [CrossRef]
  135. Fegeros, K.; Zervas, G.; Stamouli, S.; Apostolaki, E. Nutritive value of dried citrus pulp and its effect on milk yield and milk composition of lactating ewes. J. Dairy Sci. 1995, 78, 1116–1121. [Google Scholar] [CrossRef]
  136. Onwuka, C.F.I.; Adetiloye, P.O.; Afolami, C.A. Use of household wastes and crop residues in small ruminant feeding in Nigeria. Small Rumin. Res. 1997, 24, 233–237. [Google Scholar] [CrossRef]
  137. Varela, J.A.R.; Diaz-Vargas, M.; Duque-Ramírez, C.F.; Sierra, L.M.P. Dehydrated citrus pulp in rabbit feeding. Trop. Anim. Health Prod. 2023, 55, 346. [Google Scholar] [CrossRef]
  138. Hussein, E.; Alhotan, R.A.; Ebrahim, A.; Selim, S. Unraveling the potential of orange pulp for improving laying rate, egg quality, oxidative stability, fatty acids composition, and reproductive tract morphology of laying hens. Animals 2023, 13, 2199. [Google Scholar] [CrossRef] [PubMed]
  139. Goliomytis, M.; Kostaki, A.; Avgoulas, G.; Lantzouraki, D.Z.; Siapi, E.; Zoumpoulakis, P.; Simitzis, P.; Deligeorgis, S.G. Dietary supplementation with orange pulp (Citrus sinensis) improves egg yolk oxidative stability in laying hens. Anim. Feed Sci. Technol. 2018, 244, 28–35. [Google Scholar] [CrossRef]
  140. Zoidis, E.; Simitzis, P.; Kampantais, D.; Katsoulas, P.; Pappas, A.C.; Papadomichelakis, G.; Goliomytis, M. Dietary orange pulp and organic selenium effects on growth performance, meat quality, fatty acid profile, and oxidative stability parameters of broiler chickens. Sustainability 2022, 14, 1534. [Google Scholar] [CrossRef]
  141. Tripodo, M.M.; Lanuzza, F.; Micali, G.; Coppolino, R.; Nucita, F. Citrus waste recovery: A new environmentally friendly procedure to obtain animal feed. Bioresour. Technol. 2004, 91, 111–115. [Google Scholar] [CrossRef] [PubMed]
Figure 1. The major citrus producing countries (A) and citrus crops worldwide (B).
Figure 1. The major citrus producing countries (A) and citrus crops worldwide (B).
Microorganisms 13 01891 g001
Table 1. Peel content and key biomolecules and bioactive compounds of major citrus peel residues.
Table 1. Peel content and key biomolecules and bioactive compounds of major citrus peel residues.
OrangeLemonGrapefruitPomeloTangerine
Peel Portion
(% of the whole fruit)
14.3–26.0 [2,3,4]36.4–48.0 [4,5]27.8–41.0 [4,6]46.9–48.6 [4,5]24.0–55.0 [7,8]
Hesperidin (mg/g dw)21.8–48.0 [9,10]6.7–24.5 [11,12]5.0–7.2 [13,14]0.7–4.2 [15,16]21.6–41.3 [12,13]
D-Limonene
(% of the EO)
70.0–90.0 [17,18]48.6–67.1 [19,20]74.8–75.1 [21,22]67.6–84.6 [23,24]71.7–85.1 [25,26]
Pectin (%)12.5–29.1 [27,28]15.0–37.9 [29,30]22.6–27.3 [31,32]18.8–28.5 [33,34]12.8–25.6 [35,36]
Cellulose (%)9.2–11.9 [37,38]8.2–12.7 [39,40]27.2 [41]15.7–21.3 [42,43]22.5 [44]
Hemicellulose (%)10.5–14.5 [37,38]5.3–18.7 [39,40]6.3 [41]8.1 [43]6 [44]
Lignin (%)0.8–2.2 [37,38]1.7 [40]13.1 [41]0.1 [43]8.6 [44]
Lipids (%)1.9 [37]5 [45]0.2 [31]1.6 [43]1–8.7 [46,47]
Moisture (%)7 [37]11.5 [48]75 [31]16.1 [43]6.1 [46]
Ash (%)3.5 [37]1.9 [40]1.5 [31]3.4 [43]3.1–4 [46,47]
Table 2. Bioenergy recovery from citrus processing waste.
Table 2. Bioenergy recovery from citrus processing waste.
ProcessProductsReference
Anaerobic digestionBiogas (without pretreatment); Biogas of high methane yield (via D-limonene minimization)[58,59,60,61]
Dark fermentationBiohydrogen production[62,63]
Hydrothermal pretreatment + fermentationEnhanced biohydrogen production, biobutanol production[64]
Yeast fermentationBioethanol, Lipids for biodiesel production (39% lipid content) [65,66,67,68]
Lipid extraction from orange seedsLipids for biodiesel production (37% content; Fatty Acids: oleic, linoleic and palmitic acids) [69]
EnsilingLactic acid and bioethanol—Enhanced anaerobic digestibility (65% VS, 75% limonene reduction)[70,71]
Table 3. Bioconversion of citrus processing waste to soil fertility enhancers and phytoprotective agents.
Table 3. Bioconversion of citrus processing waste to soil fertility enhancers and phytoprotective agents.
ProcessProductsReference
Direct application of CPWPhytoprotection (against weeds, insects, nematodes, fungi) via essential oils[73]
Co-compostingMature compost with low phytotoxicity (mesophilic → thermophilic microbiota)[74]
Vermicomposting (with Eisenia fetida)Stabilized compost from orange waste[75]
Compost amendment to soilOptimal seedling growth (tomato, zucchini) at 7.5% compost rate[76]
Field application (4 kg/m2 orange waste)Comparable wheat yield to mineral fertilizer[77]
Application in onion fieldsWeed control and doubled onion bulb yield[78]
Extract of orange juice wasteBioherbicidal effect (weed germination inhibition/delay without harming crop biomass)[79]
Use of CPW in pesticide removalRemoval of diazinon and parathion; CPW as biosorbent[80]
Citrus essential oilInsecticidal protection against Callosobruchus maculatus on chickpeas[81]
Orange peel essential oilsControl of postharvest anthracnose (Colletotrichum gloeosporioides, C. scovillei) on mangoes[82]
CPW as fungal growth substrateCultivation of bioprotective fungi (Beauveria bassiana, Trichoderma harzianum) for biopesticide use[83]
Table 4. Bioconversion of citrus processing waste to produce biobased polymers, antimicrobial materials, and adsorbents.
Table 4. Bioconversion of citrus processing waste to produce biobased polymers, antimicrobial materials, and adsorbents.
ProcessProductsReference
Microbial growth on orange peelsPHB (bioplastic) production by Bacillus cereus (0.4 g/kg)[85]
Orange peel extract in biocomposite filmAntimicrobial and antioxidant packaging film (against Salmonella enterica and Escherichia coli)[86]
Orange peels in biopolymer compositeFunctional packaging: antioxidant and antibacterial activity[87]
Film with eggshell, pectin and orange EOAntimicrobial biocomposite (vs Staphylococcus aureus, B. cereus); good barrier and stress resistance[89]
Submerged fermentation of CPWBiosurfactant production by Bacillus haynesii E1[90]
AgNP synthesis using orange peel extractAntimicrobial silver nanoparticles (active against bacteria and fungi)[91]
Citrus chitosan-coated selenium nanocompositeAntifungal activity vs. Sclerotinia sclerotiorum (complete inhibition at 0.5 ppm)[92]
Activated carbon from CPW (TiO2-modified)Arsenic removal (10.9 mg/g, pH 4.2, 3.3 g/L dosage)[93]
Microwave-activated orange peel carbonHeavy metal removal: As (V), Se (IV), Cu (II), Cd (II)[94]
Orange peel as bioadsorbentMethylene blue dye removal (~112 mg/g capacity)[95]
Conversion to nanoporous materialsAdsorptive materials for biochemical use[96]
ZnO-orange-peel porous nanocompositeDye removal (>90% for crystal violet and methylene blue)[97]
Orange peel biocharDNA adsorption (potential to remove antibiotic resistance genes)[98]
Electrochemical nitrate sensor (Cu2O–carbon)Pollution monitoring; linear detection to 1 mM, limit: 1.2 μM[99]
Ultrasonic-treated orange peelAcoustic insulation material[100]
Table 5. Key fermentation end products of citrus processing waste.
Table 5. Key fermentation end products of citrus processing waste.
ProcessProductsReference
Biorefinery of orange peels with Weizmannia coagulans and Priestia megateriumLimonene, high-activity peroxidase, lactic acid, polyhydroxybutyrate[101]
Enzymatic bioconversion of orange peel-based agricultural residues using Aspergillus niger SKN1 and Trametes hirsuta SKH1Hydrolysate fermented into biobutanol by Clostridium acetobutylicum[102]
Fermentation of orange bagasse pellets by Clostridium beijerinckiiButanol[103]
Lactic acid fermentation by Lactobacillus casei 2246Lactic acid (0.88 g/g d.w.)[104]
Fermentation by L. delbrueckii subsp. delbrueckiiD-lactic acid[105]
Solid-state fermentation by Aspergillus oryzaeGalacturonic acid[106]
Solid-state fermentation by Aspergillus nigerCitric acid[106]
Cultivation of Euglena gracilis on orange peelsβ-glucan[107]
Solid-state fermentation by Aspergillus awamoriHydrolytic enzymes (xylanolytic, cellulolytic and pectinolytic enzymes) for juice clarification[108]
Solid-state fermentation by Aspergillus niger BTL, Fusarium oxysporum F3, Neurospora crassa DSM 1129, Penicillium decumbens sp.β-xylosidase, polygalacturonase, invertase, pectate lyase, endoglucanase[109]
Fermentation with Eupenicillium javanicumEndoglucanase, β-glucosidase, pectinase (~50 U/g), xylanase (~105 U/g)[110]
Fermentation with Trichoderma virideCellulolytic activity (>400 U/mL)[111]
Fermentation with Aspergillus brasiliensisPolygalacturonase (up to 45 U/g)[112]
Fermentation with Cladosporium spp.Endoglucanase, exoglucanase, xylanase, pectinase, amylase[113]
Fermentation of orange peels + sugar beet cossettesXylanase, exo-polygalacturonase; improved hydrolysis with added cellulases[114]
Fermentation by Botryosphaeria rhodina MAMB-05Pectinase[115]
Treatment of orange peels with Bacillus cereusα-amylase (8.5 U/mL)[116]
Fermentation with a halophilic Streptomyces sp.α-amylase (12.19 U/mL)[117]
Heterologous expression in Komagataella phaffiiRecombinant pectinase (460 U/mL)[118]
Processing by Wickerhamomyces subpelliculosusL-methioninase (94.08 U/mL)[119]
Table 6. Valorization of citrus processing waste to produce bioactive compounds.
Table 6. Valorization of citrus processing waste to produce bioactive compounds.
ProcessProductsReference
Biorefinery approach on orange peelsEssential oils, phenolics, pectin, cellulosic material[121]
Pulsed electric field treatment (7 kV/cm)Increased recovery of naringin and hesperidin[122]
Biotransformation of hesperidin from orange peelsAntioxidant diosmetin[123]
Recombinant α-L-rhamnosidase hydrolysis of naringinRhamnose[124]
Enzymatic hydrolysis combined with ultrasonic treatmentBioconversion of orange waste to β-carotene[125]
Solid-state fermentation of orange waste by Diaporthe sp.Antioxidant products from bioconversion of limonene[126]
Submerged fermentation of orange peel wasteAntioxidant and antibacterial ellagic acid (19 mg/g yield)[127]
Mixed fermentation of orange peel pomace (with microbes)Increased antioxidant capacity; biomolecules like pinoresinol, gentisic acid and quercetin derivatives[128]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Stavrakakis, I.; Melidis, P.; Kavroulakis, N.; Goliomytis, M.; Simitzis, P.; Ntougias, S. Bioeconomy-Based Approaches for the Microbial Valorization of Citrus Processing Waste. Microorganisms 2025, 13, 1891. https://doi.org/10.3390/microorganisms13081891

AMA Style

Stavrakakis I, Melidis P, Kavroulakis N, Goliomytis M, Simitzis P, Ntougias S. Bioeconomy-Based Approaches for the Microbial Valorization of Citrus Processing Waste. Microorganisms. 2025; 13(8):1891. https://doi.org/10.3390/microorganisms13081891

Chicago/Turabian Style

Stavrakakis, Ioannis, Paraschos Melidis, Nektarios Kavroulakis, Michael Goliomytis, Panagiotis Simitzis, and Spyridon Ntougias. 2025. "Bioeconomy-Based Approaches for the Microbial Valorization of Citrus Processing Waste" Microorganisms 13, no. 8: 1891. https://doi.org/10.3390/microorganisms13081891

APA Style

Stavrakakis, I., Melidis, P., Kavroulakis, N., Goliomytis, M., Simitzis, P., & Ntougias, S. (2025). Bioeconomy-Based Approaches for the Microbial Valorization of Citrus Processing Waste. Microorganisms, 13(8), 1891. https://doi.org/10.3390/microorganisms13081891

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop