Investigation into the role of endogenous abscisic acid during ripening of imported avocado cv. Hass

BACKGROUND The importance of ethylene in avocado ripening has been extensively studied. In contrast, little is known about the possible role of abscisic acid (ABA). The present work studied the effect of 1-methylcyclopropene (1-MCP) (0.3 μL L−1), e+® Ethylene Remover and the combination thereof on the quality of imported avocado cv. Hass fruit stored for 7 days at 12 °C. Ethylene production, respiration, firmness, colour, heptose (C7) sugars and ABA concentrations in mesocarp tissue were measured throughout storage. RESULTS Treatment with e+® Ethylene Remover reduced ethylene production, respiration rate and physiological ripening compared with controls. Fruit treated with 1-MCP + e+® Ethylene Remover and, to a lesser extent 1-MCP alone, had the lowest ethylene production and respiration rate and hence the best quality. Major sugars measured in mesocarp tissue were mannoheptulose and perseitol, and their content was not correlated with ripening parameters. Mesocarp ABA concentration, as determined by mass spectrometry, increased as fruit ripened and was negatively correlated with fruit firmness. CONCLUSIONS Results suggest a relationship between ABA and ethylene metabolism since blocking ethylene, and to a larger extent blocking and removing ethylene, resulted in lower ABA concentrations. Whether ABA influences avocado fruit ripening needs to be determined in future research. © 2017 Society of Chemical Industr

Onion gene expression in response to ethylene and 1-MCP

Onion is regarded as a non-climacteric vegetable. In onions, however, ethylene can suppress sprouting while the ethylene binding inhibitor, 1-MCP (1- methylcyclopropene) can also suppress sprout growth yet, it is unknown how ethylene and 1-MCP elicit the same response. In this study, onions were treated with 10 μL L-1 ethylene or 1 μL L-1 1-MCP individually or in combination for 24 h at 20°C before or after curing (six weeks) at 20 or 28°C then stored at 1°C. Following curing, a subset of these same onions was stored separately under continuous air or ethylene (10 μL L- 1) at 1°C Onions treated with ethylene and 1-MCP in combination after curing for 24 h had reduced sprout growth as compared with the control 25 weeks after harvest. Sprout growth following storage beyond 25 weeks was only reduced through continuous ethylene treatment. This observation was supported by a higher proportion of down-regulated genes characterised as being involved in photosynthesis measured using a newly developed onion microarray. Physiological and biochemical data suggested that ethylene was being perceived in the presence of 1-MCP since sprout growth was reduced in onions treated with 1-MCP and ethylene applied in combination but not when applied individually. A cluster of probes representing transcripts up-regulated by 1-MCP alone but down-regulated by ethylene alone or in the presence of 1-MCP support this suggestion. Ethylene and 1-MCP both down52 regulated a probe tentatively annotated as an ethylene receptor as well as EIN3, suggesting that both treatments down-regulate the perception and signalling events of ethylene

Understanding the mechanisms behind onion bulb dormancy in relation to the potential for improved onion storage

Onion (Allium cepa L.) is the most economically important Allium crop. Onion cultivars adapted for growth in temperate regions require long days for bulb initiation, so the summer crop is stored over-winter. Deterioration in store is largely due to resumption of growth. Extended storage of onions is currently dependent on the synthetic sprout suppressant maleic hydrazide, whose future use is uncertain due to pressure to reduce residues in foods. Abscisic acid (ABA) has previously been linked with dormancy in a relative of onion (A. wakegi). Bulb ABA concentration in three onion cultivars (viz. Renate, Ailsa Craig and SS1) with contrasting storage lives declined exponentially during controlled atmosphere (CA – 3% CO2, 5% O2; 2°C) storage at the same rate in each cultivar. Sprouting occurred at a minimal ABA concentration (ca. 50-120 ng g-1 DW). It was proposed that extended periods of high concentrations of ABA may delay sprouting. An ABA analogue (PBI-365) and exogenous ABA, were applied as preharvest foliar sprays (cvs. Renate, Carlos, Dinaro, Hysam, Red Baron and SS1), or as postharvest bulb soaks (cv. Hysam) with the aim of increasing endogenous ABA concentration and, thereby, extending the storage period. Endogenous bulb ABA concentration was not affected. Bulb ABA concentration again decreased during storage at a range of temperatures (4, 12 and 20°C) and sprouting occurred at minimal ABA concentration (ca. 75-150 ng g-1 DW). After the onset of sprouting, ABA concentration increased again, probably due to synthesis by the sprout. The concentration of certain carbohydrates has been linked with storage potential. No straightforward relationship between ABA and non-structural carbohydrate (NSC; fructose, glucose, sucrose and fructans) metabolism could be determined. It was therefore postulated that ABA is more likely to play a role in mediating cell elongation rather than cell division, or that minimal ABA concentration could be a trigger for remobilisation of carbohydrates. Controlled atmosphere (CA) is used to extend storage life of onions; however, shelf-life can be compromised. The effects of the transition between CA (3 % CO2, 5 % O2; 2°C) and air storage on ABA concentration, quality characteristics, respiration rate(RR) and NSCs in three onion cultivars (viz. Renate, Carlos and SS1) were investigated. The RR of the short storing cultivar, SS1, was greatest by ca. 0.5-fold. The RR increased on removal from CA storage, with no accompanying decrease in carbohydrate concentration, indicating that the increased RR may have been a transient stress response. Storage of onions cv. SS1 for three weeks in air, followed by three weeks CA was as effective in suppressing sprout growth as six weeks continuous CA storage. Bulb ABA concentration decreased significantly between the time of harvest and after curing. Therefore the current practice of curing onions for extended periods at high temperatures could be reducing bulb ABA concentration, and therefore storage life. The literature concerning the role of ethylene in onion storage is limited and conflicting. The effect of 1-methylcyclopropene (1-MCP; an ethylene perception inhibitor) on sprout growth in onions cv. SS1 stored at a range of temperatures (4, 12 and 20°C) was investigated, along with quality characteristics, NSCs and ABA. Sprout growth was reduced in onions treated with 1-MCP and stored at 4 or 12°C, but not at 20°C. Approximately 2-fold greater concentrations of sucrose, glucose and fructose were maintained in 1-MCP-treated bulbs stored at 12°C as compared with untreated bulbs. It appeared that 1-MCP reduced carbohydrate metabolism. Both ethylene and ABA are highly likely to impact significantly on onion storage life. The results are discussed in relation to the potential to influence storage life by changes in horticultural practices, including the recommendation to re-evaluate the curing and drying protocol, and to investigate the possibility of delaying the start of CA storage.EThOS - Electronic Theses Online ServiceGBUnited Kingdo

New insights into the effects of ethylene on ABA catabolism, sweetening and dormancy in stored potato tubers

Continuous ethylene supplementation suppresses postharvest sprouting, but it can increase reducing sugars, limiting its use as an alternative to chlorpropham for processing potatoes. To elucidate the mechanisms involved, tubers were treated after curing with or without the ethylene binding inhibitor 1-methylcyclopropene (1-MCP at 1 μL L−1 for 24 h), and then stored in air or air supplemented with continuous ethylene (10 μL L−1). Across three consecutive seasons, changes in tuber physiology were assessed alongside transcriptomic and metabolomic analysis. Exogenous ethylene alone consistently induced a respiratory rise and the accumulation of undesirable reducing sugars. The transient respiratory peak was preceded by the strong upregulation of two genes encoding 1-aminocyclopropane-1-carboxylate oxidase (ACO), typical of wound and stress induced ethylene production. Profiles of parenchymatic tissue highlighted that ethylene triggered abscisic acid (ABA) catabolism, evidenced by a steep fall in ABA levels and a transient rise in the catabolite phaseic acid, accompanied by upregulation of transcripts encoding an ABA 8ˊ-hydroxylase. Moreover, analysis of non-structural carbohydrate-related genes revealed that ethylene strongly downregulated the expression of the Kunitz-type invertase inhibitor, already known to be involved in cold-induced sweetening. All these ethylene-induced effects were negated by 1-MCP with one notable exception: 1-MCP enhanced the sprout suppressing effect of ethylene whilst preventing ethylene-induced sweetening. This study supports the conclusions that: i) tubers adapt to ethylene by regulating conserved pathways (e.g. ABA catabolism); ii) ethylene-induced sweetening acts independently from sprout suppression, and is similar to cold-induced sugar accumulation

Use of canonical variate analysis to differentiate onion cultivars by mineral content as measured by ICP-AES

Three onion cultivars viz. Renate, Ailsa Craig and SS1 were characterised according to their mineral content. The concentrations of the macronutrients phosphorus, potassium, calcium, manganese and sulphur and the micronutrients iron, boron, manganese, copper and zinc were analysed in freshly harvested and stored onion bulbs using ICP-AES (Inductively coupled plasma-atomic emission spectroscopy). Onions were treated pre-harvest with additional sulphur (100 kg ha−1) and/or calcium (300 kg ha−1) applied in four combinations at the time of seed drilling, however these treatments did not affect the total concentrations of sulphur or calcium in the harvested bulbs. The data were subjected to canonical variate analysis in order to determine the most appropriate variate to discriminate between cultivars. Two canonical variates were sufficient to differentiate between the three cultivars, with the first canonical variate describing differences in micronutrients between the genotypes and the second separating the cultivars by differences in sulphur concentra

Ethylene and 1-methylcyclopropene differentially regulate gene expression during onion sprout suppression.

Onion (Allium cepa) is regarded as a nonclimacteric vegetable. In onions, however, ethylene can suppress sprouting while the ethylene-binding inhibitor 1- methylcyclopropene (1-MCP) can also suppress sprout growth; yet, it is unknown how ethylene and 1-MCP elicit the same response. In this study, onions were treated with 10 μL L(-1) ethylene or 1 μL L(-1) 1-MCP individually or in combination for 24 h at 20°C before or after curing (6 weeks) at 20°C or 28°C and then stored at 1°C. Following curing, a subset of these same onions was stored separately under continuous air or ethylene (10 μL L(-1)) at 1°C. Onions treated with ethylene and 1-MCP in combination after curing for 24 h had reduced sprout growth as compared with the control 25 weeks after harvest. Sprout growth following storage beyond 25 weeks was only reduced through continuous ethylene treatment. This observation was supported by a higher proportion of down- regulated genes characterized as being involved in photosynthesis, measured using a newly developed onion microarray. Physiological and biochemical data suggested that ethylene was being perceived in the presence of 1-MCP, since sprout growth was reduced in onions treated with 1-MCP and ethylene applied in combination but not when applied individually. A cluster of probes representing transcripts up-regulated by 1-MCP alone but down-regulated by ethylene alone or in the presence of 1-MCP support this suggestion. Ethylene and 1-MCP both down- regulated a probe tentatively annotated as an ethylene receptor as well as ethylene-insensitive 3, suggesting that both treatments down-regulate the perception and signaling events of

Physiological, biochemical and transcriptional analysis of onion bulbs during storage

Background and Aims During the transition from endo-dormancy to eco-dormancy and subsequent growth, the onion bulb undergoes the transition from sink organ to source, to sustain cell division in the meristematic tissue. The mechanisms controlling these processes are not fully understood. Here, a detailed analysis of whole onion bulb physiological, biochemical and transcriptional changes in response to sprouting is reported, enabling a better knowledge of the mechanisms regulating post-harvest onion sprout development. Methods Biochemical and physiological analyses were conducted on different cultivars (‘Wellington’, ‘Sherpa’ and ‘Red Baron’) grown at different sites over 3 years, cured at different temperatures (20, 24 and 28 °C) and stored under different regimes (1, 3, 6 and 6 → 1 °C). In addition, the first onion oligonucleotide microarray was developed to determine differential gene expression in onion during curing and storage, so that transcriptional changes could support biochemical and physiological analyses. Key Results There were greater transcriptional differences between samples at harvest and before sprouting than between the samples taken before and after sprouting, with some significant changes occurring during the relatively short curing period. These changes are likely to represent the transition from endo-dormancy to sprout suppression, and suggest that endo-dormancy is a relatively short period ending just after curing. Principal component analysis of biochemical and physiological data identified the ratio of monosaccharides (fructose and glucose) to disaccharide (sucrose), along with the concentration of zeatin riboside, as important factors in discriminating between sprouting and pre-sprouting bulbs. Conclusions These detailed analyses provide novel insights into key regulatory triggers for sprout dormancy release in onion bulbs and provide the potential for the development of biochemical or transcriptional markers for sprout initiation. Evidence presented herein also suggests there is no detrimental effect on bulb storage life and quality caused by curing at 20 °C, producing a considerable saving in energy and costs