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Article

Phytoene and Phytoene-Rich Microalgae Extracts Extend Lifespan in C. elegans and Protect against Amyloid-β Toxicity in an Alzheimer’s Disease Model

by
Ángeles Morón-Ortiz
1,
Antonis A. Karamalegkos
2,
Paula Mapelli-Brahm
1,
Marina Ezcurra
2,*,† and
Antonio J. Meléndez-Martínez
1,†
1
Food Colour and Quality Laboratory, Facultad de Farmacia, Universidad de Sevilla, 41012 Sevilla, Spain
2
School of Biosciences, University of Kent, Canterbury CT2 7NJ, UK
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Antioxidants 2024, 13(8), 931; https://doi.org/10.3390/antiox13080931 (registering DOI)
Submission received: 25 May 2024 / Revised: 26 July 2024 / Accepted: 28 July 2024 / Published: 31 July 2024
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Abstract

:
Phytoene is a colourless carotenoid widely available from dietary sources and a precursor for the synthesis of other carotenoids. Although present at high concentrations across different tissues, phytoene is largely viewed as not having physiological activity. Here, we utilize the model organism C. elegans to show that phytoene is bioactive and has anti-ageing properties. Supplementation with phytoene protects against oxidative damage and amyloid-β42 proteotoxicity (a major pathology of Alzheimer’s disease), and extends lifespan. We also examine extracts from two microalgae, Chlorella sorokiniana and Dunaliella bardawil. We show that the extracts contain high levels of phytoene, and find that these phytoene-rich extracts have protective effects similar to pure phytoene. Our findings show that phytoene is a bioactive molecule with positive effects on ageing and longevity. Our work also suggests that phytoene-rich microalgae extracts can utilized to produce foods or supplements that promote healthy ageing and prevent the development of chronic age-related diseases.

1. Introduction

Carotenoids are widespread and versatile compounds that are precursors of derivatives termed apocarotenoids. Both carotenoids and apocarotenoids play key roles in processes that are essential for plant development and resilience (light collection and photoprotection in photosynthesis, communication between plants, pollinators, and seed dispersers, regulation of many plant processes, etc.) and are therefore essential for food security. Carotenoids also function as pigments contributing to the colours of many vegetables and fruits, and as important nutritional components of foods, e.g., as precursors of vitamin A. Many studies indicate that carotenoids have health-promoting properties and contribute to the amelioration or the reduction in the risk of developing diverse diseases (cancer, cardiovascular disease, skin and bone conditions, eye disorders, metabolic disorders, age-related macular degeneration, cognitive impairment, etc.). They can also contribute to skin health, colour, and other aesthetic parameters. Therefore, carotenoids are of great interest for the development of a variety of products for human consumption including functional foods, nutraceuticals, supplements, botanicals, cosmeceuticals, or (nutri)cosmetics [1].
The main bulk of dietary intake of carotenoids comes from plant-derived foods (mainly fruits and vegetables), although they are also present in animal-derived foods (e.g., egg yolk, salmon, mussels, dairy), food colorants, and supplements [1]. Microalgae also synthesise carotenoids, as well as many other bioactive compounds with health benefits, and are rich in polysaturated fatty acids and in essential amino acids. Compared to terrestrial plants, cultivation of microalgae is more sustainable due to their rapid growth, ease of cultivation, and non-need for agricultural land, and the commercial importance of microalgae for sustainable production of health-promoting foods is growing. Thus, microalgae are a potential source of nutrition that would reduce the need for agricultural land use, decreasing the environmental impact of food production, while improving health [2].
Biosynthesis of carotenoids occurs through the production of phytoene from geranylgeranyl pyrophosphate by the enzyme phytoene synthase. Phytoene subsequently undergoes consecutive desaturation and isomerization steps to form lycopene, which is later cyclised to α- and β-carotene. The latter two can be oxygenated to form xanthophylls such as lutein and zeaxanthin. Zeaxanthin is precursor of other typical carotenoids of green microalga, such as violaxanthin and neoxanthin (Figure 1). In contrast to most other carotenoids, phytoene is colourless, does not contribute to the characteristic colours of carotenoid-rich foods, and is generally viewed as a precursor without bioactivity in the human body. Phytoene is typically not reported in epidemiological studies and the understanding of its impact on physiology is minimal. However, a few studies have shown that daily intake of phytoene is higher than most other carotenoids, and have detected phytoene in plasma and tissues at concentrations suggesting high levels of bioavailability and bioaccumulation [3,4,5]. Whether phytoene has bioactivity affecting health is largely unknown. Moreover, nothing is known about its effect on ageing and age-related disease.
Here, we examine the bioactivity of phytoene-rich carotenoid extractions from the microalgae Dunaliella bardawil and Chlorella sorokiniana, and pure phytoene, in the model organism C. elegans. We show that phytoene protects against oxidative stress and amyloid-β toxicity in a model of Alzheimer’s disease, and extends lifespan. Phytoene-rich extracts from both microalgae species also have protective effects, similar pure phytoene. Our findings demonstrate for the first time in this model that phytoene has bioactivity and protects against ageing, and suggest that phytoene-containing microalgae can be utilized to produce foods or supplements that promote healthy ageing.
For the present study, D. bardawil and C. sorokiniana were selected. These are species from two microalgae genera that are exploited commercially and widely studied for their ability to accumulate carotenoids [2]. More specifically, both species have proven amenable for phytoene accumulation [8,9].

2. Materials and Methods

2.1. Reagents

Tert-butyl methyl ether (HPLC-grade) and CaCl2 were purchased from Honeywell (Seelze, Germany); 2-methyltetrahydrofuran (2-MeTHF), KH2PO4, Na2HPO4, KPO4, 5-fluoro-2′-deoxyuridine (FUDR), cholesterol, phytoene standard, and 5-hydroxy-1,4-naphthoquinone (juglone) from Sigma-Aldrich (Steinheim, Germany); methanol (HPLC-grade) and ethyl acetate (HPLC-grade) from VWR Chemicals (Leuven, Belgium); dimethyl sulfoxide (DMSO) was purchased from Duchefa Biochemie (Haarlem, The Netherlands); sodium chloride were obtained from Fisher Chemical (Hampton, UK). Agar, peptone, and LB media were obtained from Thermo Fisher Scientific (Hampshire, UK); MgSO4 from Melford (Suffolk, UK).

2.2. Microalgae Cultivation

Chlorella sorokiniana (211-32) was kindly provided by the algal collection of the Institute of Plant Biochemistry and Photosynthesis (IBVF-CSIC, Seville, Spain) and cultured photo-mixotrophically in liquid Tris-acetate phosphate (TAP) medium [10].
Dunaliella bardawil (UTEX 2538) was supplied from the UTEX Culture Collection of Microalgae (University of Texas, Austin, TX, USA), and cultured using Johnson’s modified medium for Dunaliella, as described by Johnson et al. (1968) [11].

2.3. Phytoene Microalgae Enrichment

Cultures of C. sorokiniana in the middle of the exponential phase were harvested by centrifugation, resuspended in fresh TAP culture medium, divided into 50 mL cultures, and incubated with 1 µg/mL of norflurazon, an inhibitor of the carotenoid pathway, for 48–72 h to induce accumulation of phytoene [9]. D. bardawil cultures were harvested in the middle of the exponential growth phase and incubated with 10 µg/mL of norflurazon [8].

2.4. Extraction of Carotenoids from Microalgae

2-MeTHF, an emerging green solvent that has proved appropriate for the extraction of carotenoids in microalga, was used [9,12]. For extraction, ultrasound-assisted extraction was applied using a frequency of 20 kHz, and amplitude of 30%, and treatment time of 2 min. Samples were centrifuged and the supernatant was transferred to another tube. The procedure was repeated until the sample showed no colour. Subsequently, the samples were concentrated in a rotary evaporator (Eppendorf Concentrator plus™, Eppendorf, Hamburg, Germany), either for use as a worm supplementation or for HPLC analysis.

2.5. HPLC Analysis

Quantification of carotenoids was carried out using an Agilent 1260 Infinity II Prime LC system (Waldbronn, Germany). This system was equipped with a diode array detector and a C30 column (3 µm, 150 × 4.6 mm) (YMC, Wilmington, NC, USA). Carotenoid extracts were dissolved in 500 µL of ethyl acetate and 10 µL were injected into the system for analysis. Phytoene was detected at 285 nm. The mobile phase consisted of a mixture of methanol, tert-butyl methyl ether, and water, delivered at a flow rate of 1 mL/min via a linear gradient, as described in a study by Stinco et al. (2019) [13]. The quantification was performed by external calibration as explained in that study.

2.6. Bacterial Growth

Bacterial growth curve methodology was implemented in order to ensure no effects of carotenoids in the growth of Escherichia coli (OP50). A growth curve was created over 24 h. A 96-well microplate assay was employed using OP50 bacteria, and absorbance was measured using a SPECTROstar Nano spectrophotometer (BMG Labtech, Ortenberg, Germany). The plate was incubated at 37 °C with shaking for 25 h. The absorbance was measured at 600 nm every 100 s for 900 cycles, and measurements repeated three time for accuracy. Three biological replicates were performed for each condition.

2.7. C. elegans Culture Methods and Strains

C. elegans were maintained at 20 °C on Nematode Growth Medium (NGM) plates seeded with Escherichia coli OP50. C. elegans strains used in this study included N2 and GMC101 dvIs100 [unc-54p::A-beta-1-42::unc-54 3′-UTR + mtl-2p::GFP], both obtained from Caenorhabditis Genetics Center (CGC, University of Minnesota).

2.8. Preparation of Experimental Plates

35 mm NGM plates were seeded 150 µL OP50 and supplemented with either 50 µL of DMSO control, or 50 µL of 0.2 µg/mL, 1 µg/mL, 2 µg/mL extraction or phytoene standard 48 h later and allowed to dry overnight.

2.9. Developmental Assays

Thirty adult C. elegans were placed on experimental plates and allowed to lay eggs for 2 h. After 52–54 h, the number of animals at L4 and adult stages was counted to evaluate effects on developmental rate. The experiment was repeated three times.

2.10. Oxidative Stress Assays

Assays were performed as previously described [14]. Egg lays were performed on experimental plates; approximately 60 h after the egg lay, 50 nematodes at L4 stage were transferred to plates with 400 µM juglone. Survival was recorded hourly over a period of 8 h. Nematodes were counted as dead if they failed to respond after stimulation with a platinum wire. Any animals that died due to bagging or crawling off the plate were censored. Experiments were carried out in triplicate.

2.11. Proteotoxicity Assay

The GMC101 strain was used in this assay. Egg lays were performed on experimental plates. Approximately 60 h after the egg lay, animals at L4 stage were transferred to new experimental plates and shifted to 25 °C to induce expression of amyloid-β42, and kept at 25 °C for the remainder of the experiment. Animals were scored every day for four days, and the numbers of paralysed and non-paralysed animals were counted. Nematodes were counted as paralysed if they were alive but failed to move forwards or backwards after stimulation with a platinum wire. Three biological replicates were performed with three plates containing 30 animals each for each condition.

2.12. Lifespan Assay

Egg lays were performed on supplemented plates for 2 h. 60 h later, thirty animals at L4 stage were transferred onto experimental plates treated with 100 µM FUDR. Survival was scored every two days until all animals were dead. Any animals that died due to bagging or crawling off the plate were censored. Three biological replicates were conducted, and each contained four technical replicates.

2.13. Statistical Analysis

Data processing and statistical evaluation were performed with GraphPad Prism, version 10.1.1 (270) (San Diego, CA, USA). Oxidative stress and proteotoxicity assays were analysed using one-way and two-way ANOVA, respectively. Development assay was analysed through Fisher’s exact test. Survival assays were analysed using Kaplan–Meier and Gehan–Breslow–Wilcoxon tests applied for statistical comparison.

3. Results

3.1. Characterisation of the Carotenoid Profile of the Extracts

To establish if phytoene has effects on health and ageing, we first prepared phytoene-rich extractions from the microalgae C. sorokiniana and D. bardawil. Phytoene enrichment was induced in C. sorokiniana and D. bardawil cultures by the addition of norflurazon. We extracted carotenoids from the cultures using the green solvent 2-methyltetrahydrofuran and ultrasound-assisted extraction, as this provides a sustainable extraction method while still giving a high yield. Carotenoid content was quantified by HPLC analysis and showed high levels of phytoene present in the extracts. Phytoene constituted 47% and 45% of the total carotenoid content in C. sorokiniana and D. bardawil extracts, respectively (Table 1). The C. sorokiniana and D. bardawil extracts, and a phytoene standard, were used to test for bioactivity throughout this study.

3.2. Effects of Phytoene-Rich Extracts on Growth of E. coli OP50

Before performing tests in C. elegans, we wanted to rule out the possibility that the extracts inhibit growth of the C. elegans food source E. coli OP50, as this could lead to reduced food availability and dietary restriction. We conducted bacterial growth assays, treating OP50 bacteria with C. sorokiniana and D. bardawil phytoene-rich extracts, and with phytoene, at concentrations of 0.2 µg/mL, 1 µg/mL, and 2 µg/mL. OD600 of the bacterial cultures was measured and used to generate growth curves. OP50 growth was not affected by any of the concentrations (Figure 2), showing that treatment with the phytoene-rich extracts, or with phytoene, does not affect the amount of food available to C. elegans.

3.3. Effects of Phytoene-Rich Extracts on Development of C. elegans

Because natural compounds can have toxic effects, we next asked if the phytoene-rich extracts have detrimental effects on C. elegans growth and development. We conducted developmental assays to detect any effects on the development of larvae into adulthood. Extracts at concentrations of 0.2 µg/mL, 1 µg/mL, and 2 µg/mL were tested and very small but statistically significant increases in the proportion of adults were found. Similar differences were found for phytoene at 1 and 2 µg/mL but not at 0.2 µg/mL (Figure 3). Together, these findings show that phytoene-rich extracts and phytoene do not exhibit any major toxicity affecting development at the tested concentrations.

3.4. Phytoene and Phytoene-Rich Extracts Protect against Oxidative Stress

Next, we asked if the extracts have beneficial effects on health of the animal. Carotenoids are known to have antioxidant properties due to mechanisms including quenching, scavenging, or modulation of gene expression [1]. We therefore tested if the phytoene-rich extracts affect sensitivity to oxidative stress in C. elegans using juglone, a naturally occurring mitochondrial toxin that generates superoxide anion radicals [15,16]. We exposed animals to 400 µM juglone and compared survival after 8 h. We found that in comparison to control conditions, supplementation with the extracts at 0.2 µg/mL) did not affect survival. In contrast, at supplementation with concentrations of 1 and 2 µg/mL, the survival rate of C. elegans was increased by 39–53%, depending on the extract and the concentration (p < 0.05) (Figure 4). Phytoene only also increased survival at the same concentrations, and to a similar extent, as the C. sorokiniana and D. bardawil extracts. These findings show that phytoene-rich microalgae extracts, as well as phytoene on its own, have antioxidant properties leading to increased resistance to oxidative stress in vivo.

3.5. Phytoene and Phytoene-Rich Extracts Protect against Proteotoxicity

To further investigate protective effects of microalgae extracts on health, we used a humanised C. elegans model of proteotoxicity expressing human amyloid-β42. In this model, amyloid-β42 leads to protein aggregation and formation of amyloid plaques, the main pathology in Alzheimer’s disease. Because the amyloid-β42 is expressed in body-wall muscle, protein aggregation leads to muscle dysfunction and paralysis of the animal. We evaluated proteotoxicity by measuring paralysis in animals supplemented with microalgae extracts at 1 µg/mL. Compared to the controls, supplementation with the extracts, and with phytoene, had a protective effect. On day 2 of the experiment, paralysis was reduced from 62% in the DMSO control to 37%, 40%, and 43% for treatments with D. bardawil and C. sorokiniana phytoene-rich extracts, and phytoene standard, respectively (p > 0.05) (Figure 5). Thus, phytoene protects C. elegans against proteotoxicity resulting from human amyloid-β42.

3.6. Phytoene and Phytoene-Rich Extracts Extend Lifespan

Both oxidative stress and proteotoxicity play central roles in ageing, and the protective effects we observed suggest that phytoene might affect ageing and longevity. We tested this by supplementing animals with the microalgae extracts and with phytoene at 1 µg/mL and conducting lifespan assays. Animals on OP50 had a median lifespan of 16.4 days, similarly to animals on DMSO, which had a median lifespan of 16.1 days. Animals supplemented with extracts from C. sorokiniana and D. bardawil had median lifespans of 17.7 and 19.1 days, an increase of 10% and 18.6%, respectively. Phytoene also extended lifespan; animals treated with phytoene had a median lifespan of 18.6 days and an increase of 15.5% (Figure 6 and Table S1). Our findings suggest that supplementation with phytoene, and phytoene-rich extracts from microalgae, results in lifespan extension in C. elegans.

4. Discussion

4.1. Insights from Analysing Bioactivity of Phytoene

In this study, we have described how phytoene, and phytoene-rich extracts from microalgae, affect resistance to oxidative stress, resistance to amyloid-β42 proteotoxicity, and lifespan in C. elegans. Our findings show that microalgae are a source of health-promoting compounds and have potential to be developed into functional foods and other products promoting health. Our study also suggests that phytoene is not only a precursor for the biosynthesis of other carotenoids, but also has biological activity in its own right, with beneficial effects on health and longevity. In our study we showed that treatment with phytoene results in anti-ageing effects to the same extent as extracts containing a mixed pool of carotenoids. To our knowledge, no other studies have directly shown that phytoene intake promotes longevity.
Epidemiological studies show that greater intake of foods rich in carotenoids is linked to improved health outcomes. For example, tomatoes are associated with reduced risks of cardiovascular disease and cancer, with these health effects mostly attributed to lycopene. Tomatoes also have high levels of phytoene, but measures of phytoene are not included in most epidemiological studies [17,18], despite some studies showing that phytoene intake is higher than other carotenoids traditionally studied in relation to health, such as lutein, zeaxanthin, or β-cryptoxanthin [3,4]. Including a wider range of measures in future epidemiological studies would uncover links between phytoene and health outcomes, and determine if lycopene is the main bioactive component in foods such as tomatoes, or a marker for consumption of foods containing other health-promoting phytochemicals.

4.2. Mechanisms by Which Phytoene Impacts Ageing

By which mechanisms does phytoene protect against oxidative stress, proteotoxicity, and ageing? Carotenoids have antioxidant effects that have been well described in plants, as well as in a large number of in vitro and in vivo experiments with human relevance [19]. Carotenoids protect against oxidative damage caused by reactive free radicals, including in disease states where oxidative damage occurs such as cancer, diabetes, atherosclerosis, obesity, arthritis, and neurodegeneration [20,21]. As already mentioned, carotenoids can act as antioxidants by directly quenching or scavenging reactive oxygen species or through the induction of the expression of genes [1]. In a study, the free radical scavenging properties of lycopene, phytofluene, and phytoene were evaluated experimentally and in silico. It was concluded that, although lycopene was the best antiradical, phytoene and phytofluene exhibited a higher antioxidant capacity than could be expected from their fewer number of conjugated double bonds (three and five, respectively, compared to 11 for lycopene) [22].
There is growing evidence supporting that carotenoids, in addition to directly interacting with reactive oxygen species, also interact with cellular targets, leading to broader effects mediated by endogenous proteins [19]. For example, lycopene and astaxanthin have been shown to inhibit the NF-κB pathway, reducing the activation of downstream pro-inflammatory genes and inflammation caused by obesity, cancer, and other diseases [23]. β-carotene, lycopene, and astaxanthin activate the transcription factor NRF2, resulting in increased expression of antioxidant and detoxification enzymes. Activation of these endogenous defence systems leads to a reduction in intracellular reactive oxygen species, carcinogens, and other toxins, and may reduce progression of cancers, cardiovascular diseases, and neurodegeneration [19]. Future studies will show if phytoene also has bioactive properties beyond scavenging reactive oxygen species.
In vivo studies in model organisms have directly demonstrated that carotenoids protect against ageing. Several studies used C. elegans and showed that supplementation with carotenoid-rich extracts from plant sources not only protect against oxidative stress but also increase lifespan [20,24,25,26,27,28,29]. Moreover, individual carotenoids improve health in C. elegans; e.g., astaxanthin protects against oxidative stress [30] and extends lifespan [31,32,33] and lycopene protects against amyloid-β42 proteotoxicity [26]. Several studies in C. elegans also confirmed that the anti-ageing effects of carotenoids require cellular targets and do not only act by directly quenching free radicals. Protection against oxidative stress by carotenoid-rich supplementation is dependent of the Nrf2 orthologue SKN-1 [28]. Lifespan extension by supplementation with Vitamin A is also dependent on the Nrf2/SKN-1 pathway [34], suggesting an important role for Nrf-2/SKN-1 in lifespan extension by carotenoid supplementation. However, individual carotenoids may act through different cellular pathways. Interestingly, astaxanthin promotes longevity in C. elegans not through Nrf2/SKN-1, but requires the transcription factor DAF-16, homolog of mammalian FOXO, a critical longevity factor across species [35]. One possibility is that phytoene also stimulates longevity pathways by activation of cellular targets that either overlap, or do not overlap, with those of other carotenoids. This warrants further investigation.

4.3. Microalgae—A Sustainable Source of Bioactive Compounds to Improve Healthy Ageing?

The role of foods is shifting from focusing on the provision of energy and basic nutrients to also include the supply of bioactive compounds capable of offering protection against the development of diseases. With the global population increasing, and demographics rapidly shifting towards ageing societies with increasing numbers of people suffering from multiple age-related chronic diseases, there is a growing demand for production of foods that meet our growing health needs, while being sustainable [36]. Microalgae are a heterogeneous group of photosynthetic microorganisms with enormous ecological importance that can be harnessed for the sustainable production of foods or ingredients. Thus, they account for approximately half of global CO2 fixation, their cultivation does not require arable land, and they grow 10–50-fold faster than plants. Moreover, they are adapted to diverse environments and can thrive in abiotic stressing conditions, including high and low temperatures, nutrient depletion, high salinity, or the presence of pollutants. In addition, microalgae have lower nutritional and water requirements compared to terrestrial plants, no requirements of herbicides or pesticides, cultivation produces less wastewater, and modulation of biosynthesis of diverse metabolites is easier. Their nutritional value (high quality proteins, unsaturated fatty acids, minerals, vitamins, bioactives) is remarkable, being used as nutritional supplements in aquaculture, human foods, or for the obtaining of food, pharmaceutical, or cosmetic ingredients [2]. In our study, we used phytoene-rich cultures of the microalgae species Chlorella sorokiniana and Dunaliella bardawil and sustainable extraction methods to demonstrate the potential of microalgae as sources for functional ingredients that promote healthy ageing, while reducing land use and increasing sustainability of food production.

5. Conclusions

Our study aimed to evaluate the effects of phytoene, and phytoene-rich microalgae extracts, on health in the model organism C. elegans. Supplementation with 0.2, 1, and 2 µg/mL of phytoene and phytoene-rich extracts did not affect development, suggesting absence of toxic effects and dietary restriction. Supplementation with 1 and 2 µg/mL, but not 0.2 µg/mL, of the extracts and pure phytoene increased resistance to juglone, a mitochondrial toxin that generates superoxide anion radicals, by 39–53%, showing that phytoene, like other carotenoids, protects against oxidative stress. To assess the effects of phytoene in the context of age-related health, we used a humanised C. elegans model of amyloid-β42 toxicity, in which in amyloid plaques, a hallmark of Alzheimer’s disease, are formed. We found that 1 µg/mL phytoene and phytoene-rich extracts reduced proteotoxic effects by 30–40%. Finally, we tested the effects of phytoene on lifespan and found that 1 µg/mL phytoene and phytoene-rich extracts increased lifespan by 10–18.6%. Together, our results demonstrate that phytoene is a bioactive compound with anti-ageing effects that promote longevity.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/antiox13080931/s1, Table S1: Lifespan data of C. elegans treated with C. sorokiniana and D. bardawil extracts and phytoene.

Author Contributions

Conceptualization, A.J.M.-M. and M.E.; methodology, M.E.; investigation, Á.M.-O., A.A.K. and P.M.-B.; resources, A.J.M.-M. and M.E.; data curation, Á.M.-O.; writing—original draft preparation, Á.M.-O.; writing—review and editing, M.E. and A.J.M.-M.; supervision, P.M.-B.; project administration, A.J.M.-M. and M.E.; funding acquisition, A.J.M.-M. and M.E. All authors have read and agreed to the published version of the manuscript.

Funding

This study was financially supported by grants PID2019-110438RB-C21 (NEWCARFOODS), funded by MCIN/AEI/10.13039/501100011033 and ERDF/EU, and BB/V011243/1 funded by BBSRC. P.M.-B. was supported by a postdoc fellowship from Consejería de Transformación Económica, Industria, Conocimiento y Universidades de la Junta de Andalucía (PAIDI 2020). Á.M.-O. was supported by a grant associated to grant PID2019-110438RB-C21 (NEWCARFOODS). A.A.K. was supported by a studentship awarded by Global Challenges Doctoral Centre, University of Kent. A.J.M.-M., Á.M.-O., and P.M.-B. are members of the Spanish Carotenoid Network (CaRed), grant RED2022-134577-T, funded by MCIN/AEI/10.13039/501100011033 and ERDF/EU.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available in the article/Supplementary Materials; further inquiries can be directed to the corresponding author.

Acknowledgments

The authors are very grateful to Rosa León-Bañares and Antonio León-Vaz for the obtaining and provision of phytoene-rich microalgal biomass.

Conflicts of Interest

A.J.M.-M. carries out consultancy work for diverse companies. A.A.K., P.M.-B., Á.M.-O., and M.E. declare no conflicts of interest.

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Figure 1. Scheme of biosynthetic steps of microalgal carotenoids (adapted from Valera J.C. et al. (2015) [6], and Lichtenthaler H.K. et al. (2012) [7]). GGPP: Geranylgeranyl pyrophosphate; PSY: Phytoene synthase; PDS: Phytoene desaturase; Z-ISO: ζ-Carotene isomerase; ZDS: ζ-Carotene desaturase; CRTISO: Carotene isomerase; LCYE: Lycopene ε-cyclase; LCYB: Lycopene β-cyclase; CYP97C3: Cytochrome P450 ε-hydroxylase; CYP97A5: Cytochrome P450 β-hydroxylase; CHYB: Carotene β-hydroxylase; BKT: β-Carotene oxygenase; ZEP: Zeaxanthin epoxidase; VDE: Violaxanthin de-epoxidase; NXS: Neoxanthin synthase.
Figure 1. Scheme of biosynthetic steps of microalgal carotenoids (adapted from Valera J.C. et al. (2015) [6], and Lichtenthaler H.K. et al. (2012) [7]). GGPP: Geranylgeranyl pyrophosphate; PSY: Phytoene synthase; PDS: Phytoene desaturase; Z-ISO: ζ-Carotene isomerase; ZDS: ζ-Carotene desaturase; CRTISO: Carotene isomerase; LCYE: Lycopene ε-cyclase; LCYB: Lycopene β-cyclase; CYP97C3: Cytochrome P450 ε-hydroxylase; CYP97A5: Cytochrome P450 β-hydroxylase; CHYB: Carotene β-hydroxylase; BKT: β-Carotene oxygenase; ZEP: Zeaxanthin epoxidase; VDE: Violaxanthin de-epoxidase; NXS: Neoxanthin synthase.
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Figure 2. Phytoene-rich extracts and phytoene do not alter growth of the C. elegans food source E. coli OP50. (A–C) Bacterial growth curves (OD600) of E. coli OP50 cultivated with 0.2 µg/mL, 1 µg/mL, and 2 µg/mL C. sorokiniana extracts (A), D. bardawil extracts (B), and phytoene standard (C). Three biological replicates were performed.
Figure 2. Phytoene-rich extracts and phytoene do not alter growth of the C. elegans food source E. coli OP50. (A–C) Bacterial growth curves (OD600) of E. coli OP50 cultivated with 0.2 µg/mL, 1 µg/mL, and 2 µg/mL C. sorokiniana extracts (A), D. bardawil extracts (B), and phytoene standard (C). Three biological replicates were performed.
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Figure 3. Phytoene-rich extracts and phytoene do not alter development of C. elegans. (A–C) Percentage of animals that have reached L4 (larval, pre-adulthood) stage and adulthood. Animals were treated with 0.2 µg/mL, 1 µg/mL, and 2 µg/mL C. sorokiniana extracts (A), D. bardawil extracts (B), and phytoene standard (C). Extracts were dissolved in DMSO. Controls were OP50: standard culture without supplementation, and DMSO: supplementation with DMSO only. Three biological replicates, n = 200–300 per condition. *, p < 0.05 with Fisher’s exact test compared to DMSO.
Figure 3. Phytoene-rich extracts and phytoene do not alter development of C. elegans. (A–C) Percentage of animals that have reached L4 (larval, pre-adulthood) stage and adulthood. Animals were treated with 0.2 µg/mL, 1 µg/mL, and 2 µg/mL C. sorokiniana extracts (A), D. bardawil extracts (B), and phytoene standard (C). Extracts were dissolved in DMSO. Controls were OP50: standard culture without supplementation, and DMSO: supplementation with DMSO only. Three biological replicates, n = 200–300 per condition. *, p < 0.05 with Fisher’s exact test compared to DMSO.
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Figure 4. Phytoene-rich extracts and phytoene increase resistance to oxidative stress. Survival after exposure to 400 µM juglone scored after exposure for 8 h shown. OP50: Controls grown in standard conditions without supplementation; DMSO: Control supplemented with DMSO; CHL: C. sorokiniana extracts dissolved in DMSO; DUN: D. bardawil extracts dissolved in DMSO; PT: Phytoene dissolved in DMSO. Data are represented as mean ± SD from three independent experiments with total number of animals n > 150 for each condition. *, p < 0.05 versus the control (DMSO) indicate statistically significant differences (p < 0.05) between conditions with one-way ANOVA.
Figure 4. Phytoene-rich extracts and phytoene increase resistance to oxidative stress. Survival after exposure to 400 µM juglone scored after exposure for 8 h shown. OP50: Controls grown in standard conditions without supplementation; DMSO: Control supplemented with DMSO; CHL: C. sorokiniana extracts dissolved in DMSO; DUN: D. bardawil extracts dissolved in DMSO; PT: Phytoene dissolved in DMSO. Data are represented as mean ± SD from three independent experiments with total number of animals n > 150 for each condition. *, p < 0.05 versus the control (DMSO) indicate statistically significant differences (p < 0.05) between conditions with one-way ANOVA.
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Figure 5. Phytoene and phytoene-rich extracts increase resistance to proteotoxicity. Paralysis of C. elegans expressing amyloid-β42. OP50: Controls grown in standard conditions without supplementation; DMSO: Control supplemented with DMSO; CHL: C. sorokiniana [1 µg/mL] dissolved in DMSO; DUN: D. bardawil [1 µg/mL] dissolved in DMSO; PT: Phytoene [1 µg/mL] dissolved in DMSO. Data are represented as mean ± SD from three independent experiments with total number of animals n > 90 for each condition. ***, p < 0.001; ns: Not significant with two-way ANOVA.
Figure 5. Phytoene and phytoene-rich extracts increase resistance to proteotoxicity. Paralysis of C. elegans expressing amyloid-β42. OP50: Controls grown in standard conditions without supplementation; DMSO: Control supplemented with DMSO; CHL: C. sorokiniana [1 µg/mL] dissolved in DMSO; DUN: D. bardawil [1 µg/mL] dissolved in DMSO; PT: Phytoene [1 µg/mL] dissolved in DMSO. Data are represented as mean ± SD from three independent experiments with total number of animals n > 90 for each condition. ***, p < 0.001; ns: Not significant with two-way ANOVA.
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Figure 6. Phytoene-rich extracts and phytoene extend lifespan. Survival curves of C. elegans treated with phytoene and phytoene-rich extracts. CHL: C. sorokiniana [1 µg/mL]; DUN: D. bardawil [1 µg/mL]; PT: Phytoene [1 µg/mL]. Data are represented as composites of three replicates, with median lifespan indicated in parenthesis. Total number of animals n > 120 for each condition. ***, p < 0.001; ns: Not significant and #, p = 0.0399, comparing phytoene-enriched D. bardawil and phytoene-enriched C. sorokiniana extracts with Kaplan–Meier and Gehan–Breslow–Wilcoxon tests.
Figure 6. Phytoene-rich extracts and phytoene extend lifespan. Survival curves of C. elegans treated with phytoene and phytoene-rich extracts. CHL: C. sorokiniana [1 µg/mL]; DUN: D. bardawil [1 µg/mL]; PT: Phytoene [1 µg/mL]. Data are represented as composites of three replicates, with median lifespan indicated in parenthesis. Total number of animals n > 120 for each condition. ***, p < 0.001; ns: Not significant and #, p = 0.0399, comparing phytoene-enriched D. bardawil and phytoene-enriched C. sorokiniana extracts with Kaplan–Meier and Gehan–Breslow–Wilcoxon tests.
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Table 1. Concentrations (μg/g DW) of carotenoids in C. sorokiniana and D. bardawil extracts.
Table 1. Concentrations (μg/g DW) of carotenoids in C. sorokiniana and D. bardawil extracts.
CarotenoidC. sorokinianaD. bardawil
Lutein119.44 ± 5.6377.94 ± 8.52
Zeinoxanthin1.79 ± 0.182.08 ± 0.39
Antheraxanthin4.76 ± 0.463.17 ± 0.29
Zeaxanthinn.d.14.38 ± 1.52
α-Carotene6.61 ± 0.6n.d.
β-Carotene12.12 ± 1.1412.78 ± 0.42
(9Z)-β-Carotene1.77 ± 0.121.66 ± 0.22
(15Z)-Phytoene117.86 ± 10.4499.68 ± 2.4
(All-E)-Phytoene5.05 ± 0.4312.01 ± 0.65
TCC259.91 ± 25.37246.34 ± 21.14
n.d.: not detected. TCC: Total Carotenoid Content.
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Morón-Ortiz, Á.; Karamalegkos, A.A.; Mapelli-Brahm, P.; Ezcurra, M.; Meléndez-Martínez, A.J. Phytoene and Phytoene-Rich Microalgae Extracts Extend Lifespan in C. elegans and Protect against Amyloid-β Toxicity in an Alzheimer’s Disease Model. Antioxidants 2024, 13, 931. https://doi.org/10.3390/antiox13080931

AMA Style

Morón-Ortiz Á, Karamalegkos AA, Mapelli-Brahm P, Ezcurra M, Meléndez-Martínez AJ. Phytoene and Phytoene-Rich Microalgae Extracts Extend Lifespan in C. elegans and Protect against Amyloid-β Toxicity in an Alzheimer’s Disease Model. Antioxidants. 2024; 13(8):931. https://doi.org/10.3390/antiox13080931

Chicago/Turabian Style

Morón-Ortiz, Ángeles, Antonis A. Karamalegkos, Paula Mapelli-Brahm, Marina Ezcurra, and Antonio J. Meléndez-Martínez. 2024. "Phytoene and Phytoene-Rich Microalgae Extracts Extend Lifespan in C. elegans and Protect against Amyloid-β Toxicity in an Alzheimer’s Disease Model" Antioxidants 13, no. 8: 931. https://doi.org/10.3390/antiox13080931

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