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Review

Nitric Oxide Acts as an Inhibitor of Postharvest Senescence in Horticultural Products

by
Yongchao Zhu
1,2,*,
Mei Du
1,
Xianping Jiang
2,
Miao Huang
2 and
Jin Zhao
2,*
1
Key Laboratory of Plant Resource Conservation and Germplasm Innovation in Mountainous Region (Ministry of Education), Guizhou University, Guiyang 550025, China
2
College of Agriculture, Guizhou University, Guiyang 550025, China
*
Authors to whom correspondence should be addressed.
Int. J. Mol. Sci. 2022, 23(19), 11512; https://doi.org/10.3390/ijms231911512
Submission received: 3 September 2022 / Revised: 23 September 2022 / Accepted: 26 September 2022 / Published: 29 September 2022
(This article belongs to the Special Issue Nitric Oxide Signalling and Metabolism in Plants)
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Abstract

:
Horticultural products display fast senescence after harvest at ambient temperatures, resulting in decreased quality and shorter shelf life. As a gaseous signal molecule, nitric oxide (NO) has an important physiological effect on plants. Specifically, in the area of NO and its regulation of postharvest senescence, tremendous progress has been made. This review summarizes NO synthesis; the effect of NO in alleviating postharvest senescence; the mechanism of NO-alleviated senescence; and its interactions with other signaling molecules, such as ethylene (ETH), abscisic acid (ABA), melatonin (MT), hydrogen sulfide (H2S), hydrogen gas (H2), hydrogen peroxide (H2O2), and calcium ions (Ca2+). The aim of this review is to provide theoretical references for the application of NO in postharvest senescence in horticultural products.

1. Introduction

NO is a redox-active gaseous compound that regulates diverse physiological processes in plants. Numerous studies have demonstrated a regulatory role of NO in seed germination [1], adventitious root formation [2], fruit ripening [3], abiotic stress [4,5,6,7], and biotic stress [8,9].
Horticultural products undergo rapid senescence after harvest at ambient temperatures. Postharvest senescence is an important biological process for fresh horticultural products, accompanied by a series of materials and energy metabolism, including cell wall softening [10], chlorophyll degradation [11], new pigment (carotenoid, lutein, and flavonoid) synthesis [10,11,12], volatile accumulation [13], and the change in soluble substance content [12,13,14]. Senescent products are susceptible to fungal pathogens, which lead to decay and a decline in quality. According to statistics from 2017, the average postharvest loss rate is about 15% to 20% due to postharvest senescence, resulting in a large amount of postharvest loss of fresh horticultural products, which seriously affects the commodity value and economic income.
Currently, the role of NO in postharvest senescence has been widely reported in cut flowers [15,16], vegetables [17], and fruits [18,19]. Studies have shown that NO plays an essential role in preventing postharvest senescence. As a result, we systematically reviewed and summarized the production of NO and the regulatory role of NO during the postharvest senescence process in plants for a deeper understanding of the mechanisms of NO-alleviated postharvest senescence.

2. NO Production in Plants

In higher plants, NO is generated through two pathways: enzymatic and non-enzymatic reaction pathways. The enzymatic reduction pathway is catalyzed by NAD(P)H-dependent nitrate reductase (NR) in the presence of nitrite to form NO [20]. In the enzymatic oxidation pathway, NO is primarily formed by the catalysis of NO synthase-like (NOS) activity; it can also be formed by the oxidation of S-nitroso glutathione or polyamine metabolism, but this pathway of NO production has not been well elaborated in plant cells [21]. Apart from NR and NOS, the production of NO is also catalyzed by other enzymes. By way of example, xanthine oxidoreductase (XOR) can catalyze the reduction of nitrates and nitrites to NO [22]. NO can be generated either by non-enzymatic chemical reduction of nitrite at acidic pH or by light-driven reactions in the presence of carotenoids [23,24]. Furthermore, NO can also be a byproduct of denitrification and nitrification of NH4+ [25].

3. NO Delays Postharvest Senescence

Horticultural plants are prone to rapid senescence after postharvest storage at ambient temperature. Postharvest senescence is affected by several factors, such as temperature [26], light [27,28], and some plant growth regulators [29,30,31]. Multiple studies have shown that NO is an effective way to delay postharvest senescence.

3.1. Exogenous NO Delays Postharvest Senescence

The effect of NO on alleviation of postharvest senescence can be demonstrated by the exogenous application of NO on postharvest plants. In exogenous NO treatment, three methods are available: fumigation, immersion, and spraying. Fumigation with direct NO gas delayed the senescence in postharvest mangoes and peaches [32,33]. The immersion of NO gas solution and NO donor sodium nitroprusside (SNP) or S-nitrosoglutathione (GSNO) solution also delays the postharvest senescence in some fruits by inhibiting ethylene production and reducing respiration rates [34,35]. Additionally, spraying NO donor GSNO solution is commonly used to extend the postharvest life of blueberries by improving their concentrations of ascorbic acid and glutathione [36]. The effects of exogenous NO on delaying postharvest senescence in horticultural products are listed in Table 1.

3.2. Endogenous NO Production during Postharvest Senescence Process

The effect of NO on postharvest senescence can also be revealed by endogenous NO production during postharvest senescence processes delayed by environmental factors and some chemical substances. For example, UV-B treatment can maintain decreased fruit firmness and delay postharvest senescence in mangoes by enhancing endogenous NO levels [43]. Endogenous NO production and NOS activity were induced by 1-methylcyclopropene (1-MCP) in the senescence process in cut roses [16]. Likewise, melatonin (MT) led to an increase in NO content through an increase in NOS activity and upregulation of PcNOS transcript levels, which subsequently delayed senescence in peaches [37]. However, in cold-stored peaches, abscisic acid (ABA) can induce endogenous NO synthesis via the NR pathway [44]. Similarly, NO production was also triggered by hydrogen gas (H2) by enhancing NR activity, which mitigated postharvest senescence in cut rose flowers [45].

4. The Mechanism of NO-Regulated Postharvest Senescence

NO delays postharvest senescence by regulating various metabolism pathways, including ethylene biosynthesis, respiratory metabolism, cell wall metabolism, reactive oxygen species (ROS) metabolism, and energy metabolism (Figure 1). Moreover, a set of senescence-associated genes (SAGs) that drive postharvest senescence are regulated by NO during postharvest senescence processes.

4.1. The Inhibition of Ethylene (ETH) Biosynthesis

It is well known that an increase in endogenous ETH is a sign of senescence. Thus, inhibiting endogenous ethylene production is considered a useful method to delay postharvest senescence. Exogenous NO can inhibit ETH production, which delays postharvest senescence of horticultural products, including mangoes [32,33], peaches [33], and cut rose flowers [16]. In addition, the inhibition of ETH biosynthesis-related enzymes 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase (ACO) and ACC synthase (ACS) activity and their expression levels is associated with NO-induced decreases in the endogen ETH during the postharvest senescence process [32,34]. Therefore, the positive effect of NO on postharvest senescence is largely dependent on the inhibition of the ETH biosynthesis pathway.

4.2. The Decrease of Respiratory Metabolism

Climacteric transition is generally regarded as an important signal of the initiation of senescence in climacteric plants, which affects the storage life of postharvest plants. Reducing the respiratory rate can effectively delay postharvest senescence and prolong the shelf life of horticultural crops. A previous study showed that NO treatment restrained the increase in the respiration rate and extended the postharvest life of water bamboo shoots [17]. The application of 10 μL of NO gas fumigation significantly inhibited the respiratory rate of climacteric plums and peaches, thereby extending their shelf life [33,46]. Rather than suppressing the respiratory rate of climacteric fruits, NO was also shown to depress the respiratory rate of non-climacteric fruit. For example, the respiratory rate was significantly inhibited by NO treatment throughout the entire storage period of winter jujube fruit [47].

4.3. The Activation of Cell Wall Metabolism

Generally, senescent fruits exhibit the symptom of softening as a result of cell wall degradation. Several degrading enzymes, including polygalacturonase (PG) and pectin methylesterase (PME), are involved in the degradation of the cell wall [48]. Changes in cell wall metabolism-related enzyme activity are responsible for the decrease in firmness affected by a set of abiotic factors. The application of exogenous NO maintains the decrease in firmness and extends the postharvest life of blueberries [36]. Similarly, cornelian cherries treated with 500 μM of NO donor SNP exhibited higher firmness, possibly resulting from the lower activity of PE and PME, which degrade cell walls [49]. A decrease in the NO-induced activities of PG, PME, and β-galactosidase (β-Gal) delayed postharvest winter jujube fruit softening as well [50]. At the transcript level, NO treatment suppressed the softening of postharvest tomatoes by downregulating the gene expression levels of LePG, LePhy1, and LePME [34]. In summary, NO can inhibit cell wall metabolism-related enzyme activities, which maintains the decrease in firmness of horticultural products during the NO-delayed postharvest senescence process.

4.4. The Regulation of ROS Metabolism

Postharvest senescence is often accompanied by increased ROS, followed by the induction of some SAGs. The increase in ROS level occurs in parallel with increases in lipid peroxidation in senescent cells. In addition to endogenous ROS, ROS-related antioxidant enzymes are also related to postharvest senescence. Extensive research has shown that NO can delay postharvest senescence by decreasing ROS levels and enhancing antioxidant activities. Exogenous NO fumigation reduces ROS, O2•−, and hydrogen peroxide (H2O2) contents but increases superoxide dismutase (SOD), peroxidase (POD), ascorbate peroxidase (APX), glutathione reductase (GR), and catalase (CAT) gene expression and enzymes activity, which prolongs the shelf life of table grape and appears to be strongly linked to the lipid peroxidation of membranes [51]. Likewise, NO enhances ROS scavenging capacity through the increased activity of SOD, CAT, APX, and GR, which are capable of diminishing the accumulation of O2•− and H2O2, thereby delaying the senescence of winter jujube [47]. Therefore, NO can decrease the accumulation of ROS and enhance the antioxidant system, which leads to delayed senescence in postharvest horticultural crops.

4.5. The Promotion of Energy Metabolism

The lack of energy caused by the impaired respiratory chain and reduced ATP synthesis leads to cellular breakdown and dysfunction during the postharvest senescence stage [52]. The maintenance of cellular ATP and energy levels can thus maintain the normal physiological activities of the tissues, thereby postponing postharvest senescence and prolonging the shelf life of horticultural products. Several studies have established that NO-delayed postharvest senescence is ascribed to the optimization of energy metabolism. NO treatment, for example, delayed the softness and weight loss of water bamboo by maintaining the integrity of the mitochondrial ultrastructure and enhancing ATP levels [17]. Furthermore, NO donor SNP treatment enhanced ATP synthase activity, ATP synthase CF1 alpha subunit (AtpA) content, and AtpA expression levels in the postharvest freshness of cut lilies [53].

4.6. The Induction of SAGs

Various external and internal signals are likely to activate a set of SAGs that drive postharvest senescence. During postharvest senescence, SAGs can be induced by NO to delay senescence. These NO-induced SAGs include various transcription factors (ERFs) and some structural genes encoding enzymes related to cell wall metabolism, ethylene biosynthesis, and antioxidants. The SAGs regulated by NO during the postharvest senescence process are listed in Table 2.

5. Crosstalk between NO and Plant Growth Regulators during Postharvest Senescence

NO is generally accepted as a signaling molecule that alleviates postharvest plant senescence. Additionally, other plant growth regulators influence postharvest senescence, including ETH, ABA, MT, hydrogen sulfide (H2S), H2, H2O2, and calcium ions (Ca2+).

5.1. Crosstalk between NO and ETH

ETH, a gaseous plant hormone, is crucial for postharvest senescence. The inhibition of ETH action with NO has proven to be an excellent method for preventing postharvest senescence in cut flowers [16,59], fruits [18,38], and vegetables [34]. NO inhibits endogenous ETH production by reducing ACO activity during the postharvest senescence process in cut rose flowers and apple fruit [16,18]. Additionally, NO can suppress the synthesis of ETH and the expression of the ETH synthesis-related genes ACO1 and ACSs in postharvest fruits [18,34]. Toxicological evidence has shown that ETH attenuates the delayed effect of NO during the postharvest senescence process. For example, the effect of NO on delaying postharvest senescence was improved by ETH inhibitor 1-MCP in tomatoes [60]. Moreover, it has also been suggested that 1-MCP delays cut rose flower senescence through the promotion of NOS activity and NO production [16]. Hence, NO and ETH repress each other by inhibiting ACO/ACS and NOS activity to regulate postharvest senescence in plants, respectively (Figure 2).

5.2. Crosstalk between NO and ABA

ABA is a vital phytohormone that regulates plant growth and development as well as abiotic and biotic stress. In addition, ABA is a regulator of postharvest senescence in cut rose flowers and leafy vegetables [61,62]. ABA increased NO content, NR activity, and NR transcript levels but inhibited NOS-like activity in peaches during cold storage [44]. However, exogenous NO did not affect ABA synthesis in postharvest peaches [44]. Nevertheless, NO biosynthesis inhibitor suppressed the effect of ABA on rose senescence [61]. Thus, NO might be involved in ABA-delayed postharvest senescence as a downstream signal molecule.

5.3. Crosstalk between NO and MT

A new and multifunctional hormone, MT, delays the postharvest senescence of many vegetables, fruits, and cut flowers, including broccoli [63], strawberries [64], and carnations [65]. Studies have shown that NO is involved in MT-delayed postharvest senescence. For example, exogenous MT enhances NOS and NR activity and promotes NO production, thereby suppressing postharvest pear senescence [37]. Moreover, the delaying effect of MT on fruit senescence was eliminated by N omega-nitro-L-arginine methyl ester (L-NAME), an inhibitor of NOS activity [37]. Therefore, the NO molecule appears to be downstream of MT during the postharvest senescence process.

5.4. Crosstalk between NO and H2

H2, a new signaling molecule, has been found to be involved in important physiological processes in plants, including germination [66], lateral and adventitious rooting [67,68], and plant tolerance against abiotic stress [69,70,71]. Recently, the roles of H2 in delaying postharvest senescence have been reported in cut flowers [72,73], fruits [74,75], and vegetables [76,77]. Similar to the role of H2 in adventitious root development [78] and stomatal closure [79], in which NO is involved, crosstalk between H2 and NO has also been reported during the postharvest senescence process. For example, the positive effect of H2 on alleviating the postharvest senescence of cut lilies was retarded by NO inhibitors [53]. Additionally, the generation of NO induced by H2 through the promotion of NR activity also delayed the postharvest senescence and prolonged the vase life of cut roses [45]. Thus, NO may be a downstream signaling molecule in H2-delayed postharvest senescence in plants (Figure 3).

5.5. Crosstalk between NO and H2S

The messenger molecule H2S is considered crucial to the process of postharvest senescence in plants [80,81,82]. Postharvest senescence is characterized by complex interactions between H2S and other messengers, such as NO. Recent studies suggest that H2S and NO have both synergistic and antagonistic effects on the postharvest senescence of plants. Cotreatment with H2S and NO delays postharvest senescence of strawberries and is better than H2S and NO treatments separately, suggesting a synergistic effect of H2S and NO [83]. Similarly, H2S has been shown to play a synergistic role with NO in delaying postharvest senescence in peach fruit [84]. Conversely, a study on NO delaying peach postharvest senescence through decreasing H2S content demonstrated an antagonistic relationship between H2S and NO [85]. Additionally, the H2S content of sweet pepper fruit increased, while the NO content decreased during the ripening process [86]. The interaction between H2S and NO differs between species, treatment methods, and developmental stages. However, further investigation into how H2S and NO interact during postharvest senescence is needed.

5.6. Crosstalk between NO and H2O2

H2O2 is generally regarded as an ROS that is a central regulator of plant physiological processes. H2O2 is also required for postharvest senescence in cut flowers [87]. The overproduction of endogenous H2O2 is not beneficial for delaying postharvest senescence in cut flowers [88]. Thus, inhibiting H2O2 accumulation is a useful method to delay postharvest senescence. Applying NO can prevent wound-induced browning and delay senescence by inhibiting the over-accumulation of H2O2 in fresh-cut lettuce [42]. In table grapes, NO activates catalase (CAT) activity and increases the transcript level of CAT to effectively decompose H2O2, which delays the postharvest senescence of fruit [51]. However, whether H2O2 delays postharvest senescence through the regulation of NO metabolism remains unclear.

5.7. Crosstalk between NO and Ca2+

Ca2+ is a secondary messenger that plays a critical role in horticultural products’ senescence after harvest [89]. Several recent studies have indicated that Ca2+ interacts with NO during the postharvest senescence process. The application of the NO donor S-nitro-N-acetyl-penicillamine (SNAP) delays postharvest senescence and prolongs the vase life of cut lily flowers with increased Ca2+ and calmodulin (CaM) contents [15]. A Ca2+ chelator, Ca2+ channel inhibitor, and CaM antagonist reversed the NO-induced positive effect on cut lily flowers as well [15]. Accordingly, Ca2+/CaM may function as downstream molecules of NO during postharvest senescence.
To summarize, evidence has shown that NO can delay postharvest senescence and prolong shelf life by constructing an interacted network with other signaling molecules, including ethylene, ABA, H2S, MT, H2, H2O2, and Ca2+. Within this network, NO acts either as a downstream signaling molecule of some molecules (ABA, MT, and H2) by regulating NOS and NR activities and expression levels or as an upstream signal transducer of some molecules Ca2+/CaM and H2O2 (Figure 4). Nevertheless, NO and other signaling molecules (ETH and H2S) appear to cascade in a two-sided manner (Figure 4). Furthermore, ERFs might be involved in NO-regulated metabolism changes, including cell wall, respiratory, energy, and ROS metabolism, which delay postharvest senescence (Figure 4).

6. Conclusions and Outlook

In conclusion, NO generated by enzymatic (NOS and NR) and non-enzymatic reaction pathways is involved in delaying postharvest senescence in horticultural crops. Additionally, postharvest senescence can be delayed by the exogenous application of NO donors in cut flowers, vegetables, and fruits. A set of metabolism pathways, including ethylene biosynthesis, respiratory metabolism, cell wall metabolism, reactive oxygen species (ROS) metabolism, and energy metabolism, are regulated by NO, which is associated with postharvest senescence. Moreover, the crosstalk mechanisms between NO and other molecules (ETH, ABA, MT, H2S, H2, H2O2, and Ca2+) during the postharvest senescence process were reviewed.
Although complex interactions between NO and other molecules have been observed, additional research is needed to determine how these signaling molecules influence NO biosynthesis metabolism and how NO regulates the metabolism of other molecules. Moreover, we need to discover whether other signaling molecules are interconnected in this network.

Author Contributions

Conceptualization, Y.Z.; Collection and analysis of bibliography, Y.Z., J.Z., M.D., X.J. and M.H.; Writing original draft, Y.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by Guizhou Provincial Science and Technology Projects (grant number ZK (2022) normal 160 and (2020)1Y112); the National Nature Science Foundation of China (32260799); the Natural Science Special Foundation of Guizhou University (grant number (2021)19); the Outstanding Young Scientist Program of Guizhou Province (grant number KY (2021)028) and Cultivation Research Program of Guizhou University (grant number (2019)42).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

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Ijms 23 11512 g001 550
Figure 1. NO-regulated metabolism pathways during postharvest senescence. ACO, 1-aminocyclopropane-1-carboxylic acid oxidase; ACS, 1-aminocyclopropane-1-carboxylic acid synthase; APX, ascorbate peroxidase; CAT, catalase; CCO, cytochrome oxidase; ETH, Ethylene; GR, glutathione reductase; MDH, malic acid dehydrogenase; NO, nitric oxide; PG, polygalacturonase; PME, pectinmethylesterase; POD, peroxidase; ROS, reactive oxygen species; SDH, succinic dehydrogenase; SOD, superoxide dismutase; β-Gal, β-galactosidase. Upward arrow indicates up-regulation; Downward arrow indicates down-regulation.
Figure 1. NO-regulated metabolism pathways during postharvest senescence. ACO, 1-aminocyclopropane-1-carboxylic acid oxidase; ACS, 1-aminocyclopropane-1-carboxylic acid synthase; APX, ascorbate peroxidase; CAT, catalase; CCO, cytochrome oxidase; ETH, Ethylene; GR, glutathione reductase; MDH, malic acid dehydrogenase; NO, nitric oxide; PG, polygalacturonase; PME, pectinmethylesterase; POD, peroxidase; ROS, reactive oxygen species; SDH, succinic dehydrogenase; SOD, superoxide dismutase; β-Gal, β-galactosidase. Upward arrow indicates up-regulation; Downward arrow indicates down-regulation.
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Figure 2. Model for the crosstalk between ETH and NO during the postharvest senescence process. The ‘Yin–Yang’ symbol represents the balance of ETH and NO generation through ACS/ACO and NOS pathways, respectively. ACO, 1-aminocyclopropane-1-carboxylic acid oxidase; ACS, 1-aminocyclopropane-1-carboxylic acid synthase; ETH, ethylene; NO, nitric oxide; NOS, NO synthase.
Figure 2. Model for the crosstalk between ETH and NO during the postharvest senescence process. The ‘Yin–Yang’ symbol represents the balance of ETH and NO generation through ACS/ACO and NOS pathways, respectively. ACO, 1-aminocyclopropane-1-carboxylic acid oxidase; ACS, 1-aminocyclopropane-1-carboxylic acid synthase; ETH, ethylene; NO, nitric oxide; NOS, NO synthase.
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Figure 3. Schematic model depicting the requirement of NO in H2-delayed senescence of cut flowers. APX, ascorbate peroxidase; CAT, catalase; H2, hydrogen gas; NO, nitric oxide; NR, nitrate reductase; POD, peroxidase; SOD, superoxide dismutase.
Figure 3. Schematic model depicting the requirement of NO in H2-delayed senescence of cut flowers. APX, ascorbate peroxidase; CAT, catalase; H2, hydrogen gas; NO, nitric oxide; NR, nitrate reductase; POD, peroxidase; SOD, superoxide dismutase.
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Figure 4. The crosstalk between NO and other molecules. ABA, abscisic acid; ACO, 1-aminocyclopropane-1-carboxylic acid oxidase; ACS, 1-aminocyclopropane-1-carboxylic acid synthase; Ca2+, calcium ion; CAT, catalase; CaM, calmodulin; ERFs, ethylene response factors; ETH, ethylene; H2O2, hydrogen peroxide; H2S, hydrogen sulfide; H2, hydrogen gas; MT, melatonin; NO, nitric oxide; NOS, nitric oxide synthase; NR, nitrate reductase. Red arrow indicates promotion; green arrow indicates inhibition; red two-way arrow indicates synergistic role; green two-way arrow indicates antagonistic role.
Figure 4. The crosstalk between NO and other molecules. ABA, abscisic acid; ACO, 1-aminocyclopropane-1-carboxylic acid oxidase; ACS, 1-aminocyclopropane-1-carboxylic acid synthase; Ca2+, calcium ion; CAT, catalase; CaM, calmodulin; ERFs, ethylene response factors; ETH, ethylene; H2O2, hydrogen peroxide; H2S, hydrogen sulfide; H2, hydrogen gas; MT, melatonin; NO, nitric oxide; NOS, nitric oxide synthase; NR, nitrate reductase. Red arrow indicates promotion; green arrow indicates inhibition; red two-way arrow indicates synergistic role; green two-way arrow indicates antagonistic role.
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Table
Table 1. Effects of NO on postharvest senescence in horticultural products.
Table 1. Effects of NO on postharvest senescence in horticultural products.
SpeciesTreatmentNO-Mediated EffectReferences
Pear100 μM L−1
SNP		Decreased the transcript levels of cell wall- and ethylene synthetase-related genes; reduced respiration rate and ethylene production[37]
Apple100 μM L−1
GSNO		Activated nucleocytoplasmic MdERF5 and suppressed ethylene biosynthesis[18]
Strawberry5 μM L−1
SNP		Inhibited ethylene production, respiration rate, and activity of ACC synthase; reduced the content of ACC[38]
Peach10 μL L−1
NO		Maintained higher sucrose content but decreased glucose and fructose to lower levels during late storage[33]
Carnation0.1 mM L−1
SNP		Maintained water metabolism and antioxidative enzyme activity and mass-eliminated ROS as well as cell membrane stability[39]
Rose200 μM L−1
SNP		Decreased ethylene output by inhibiting ACO activity in cut rose flowers[16]
Lily100 μM L−1
SNAP		Increased Ca2+/CaM contents, enhanced Ca2+-ATPase activity, and up-regulated gene expression of CaM, CBL1, and CBL3[15]
Consolida ajacis L.40 μM L−1
SNP		Alleviated deteriorative postharvest changes by modulating physiological and biochemical mechanisms underlying senescence[40]
Calendula
officinalis L.		100 μM L−1
SNP		Improved flower longevity by delaying neck bending, inhibited bacterial growth, and increased activities of antioxidant enzymes [41]
Tomato1 mM L−1
SNP		Retarded pericarp reddening of tomato fruit, suppressed ethylene production, and influenced quality parameters during storage[34]
Water bamboo shoots30 μL L−1
NO		Delayed softness and weight loss and enhanced ATP levels by activating the expression and activity of SDH, MDH, and CCO[17]
Lettuce100 and 200 ppm NOInhibited the accumulation of H2O2, delayed senescence, and prolonged shelf life[42]
Table
Table 2. NO-regulated SAGs during postharvest senescence process.
Table 2. NO-regulated SAGs during postharvest senescence process.
Horticultural ProductsSpeciesSAGsReferences
FruitsPearPcPG, PcCel, PcACO1, PcACO2, PcACS1, PcNOS, PcNR1, and PcNR2[37]
AppleMdACS1, MdACO1, MdERF5, and MdPP2C57[18]
MangoMiACO, MiACS, MiETR1, MiERS1, MiEIN2, and MiERF[54]
Table grapeVvSOD, VvCAT, VvPOD2, and VvGR[51]
KiwifruitPG, PL, β-Gal, PE, ACO, ERS1, ETR2, ERF016, ERF7, ERF010, ERF062, ERF110, ERF037, ERF008, ERF113, ERF12, ERF095, CNGC1, CPK1, CIPK2, CML31, CML48, and ZIFL1[55]
Wax applePAL, POD, GLU, C3H, CA, F5H, 4CL, CCoAOMT, and C4H[56]
PeachPpaSOD, PpaCAT, PpaPOD, PpaPOD-1, PpaAPX, and PpaPAL[57]
Cut flowersGladiolusGgCyP1 and GgDAD1[58]
LilyCaM, CBL1, CBL3, and LlatpA[15,53]
VegetablesTomatoLeACS2, LeACS4, LeACO1, LePME, LePG, LePhy1, and LeGAPDH[34]
Water bamboo shootsZlH+-ATPase, ZlNa+-K+-ATPase, ZlCa2+-ATPase, ZlMDH, ZlSDH, and ZlCCO[17]
4CL, 4-coumarate−CoA ligase; ACO, 1-aminocyclopropane-1-carboxylic acid oxidase; ACS, 1-aminocyclopropane-1-carboxylic acid synthase; APX, ascorbate peroxidase; AtpA, ATP synthase CF1 alpha subunit; C3H, p-coumarate 3-hydroxylase; C4H, trans-cinnamate 4-monooxygenase; CA, coniferyl-aldehyde dehydrogenase; CaM, calmodulin; CAT, catalase; CBL, calcineurin B-like protein; CCO, cytochrome oxidase; CCoAOMT, caffeoyl-CoA O-methyltransferase; Cel, cellulase; CIPK, calcineurin B-like protein-interacting protein kinase; CML, calmodulin-like protein; CNGC, cyclic nucleotide-gated channel; CPK, calcium-dependent protein kinase; CyP, cysteine protease; DAD, defender against death; EIN, ethylene insensitive; ERF, ethylene response factor; ERS, ethylene response sensor; ERT, ethylene receptor; F5H, ferulate-5-hydroxylase; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; GLU, β-glucosidase; GR, glutathione reductase; MDH, malic acid dehydrogenase; NOS, nitric oxide synthase; NR, nitrate reductase; PAL, phenylalanine ammonia-lyase; PE, pectin esterase; PG, polygalacturonase; Phy, phytoene synthase; PL, pectate lyase; PME, pectin methylesterase; POD, peroxidase; SAGs, senescence associated genes; SDH, succinic dehydrogenase; SOD, superoxide dismutase; ZIFL, calmodulin-binding heat-shock protein; β-Gal, β-galactosidase.
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Zhu, Y.; Du, M.; Jiang, X.; Huang, M.; Zhao, J. Nitric Oxide Acts as an Inhibitor of Postharvest Senescence in Horticultural Products. Int. J. Mol. Sci. 2022, 23, 11512. https://doi.org/10.3390/ijms231911512

AMA Style

Zhu Y, Du M, Jiang X, Huang M, Zhao J. Nitric Oxide Acts as an Inhibitor of Postharvest Senescence in Horticultural Products. International Journal of Molecular Sciences. 2022; 23(19):11512. https://doi.org/10.3390/ijms231911512

Chicago/Turabian Style

Zhu, Yongchao, Mei Du, Xianping Jiang, Miao Huang, and Jin Zhao. 2022. "Nitric Oxide Acts as an Inhibitor of Postharvest Senescence in Horticultural Products" International Journal of Molecular Sciences 23, no. 19: 11512. https://doi.org/10.3390/ijms231911512

APA Style

Zhu, Y., Du, M., Jiang, X., Huang, M., & Zhao, J. (2022). Nitric Oxide Acts as an Inhibitor of Postharvest Senescence in Horticultural Products. International Journal of Molecular Sciences, 23(19), 11512. https://doi.org/10.3390/ijms231911512

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