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  • Author or Editor: Lili Zhou x
  • Journal of the American Society for Horticultural Science x
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Papaya (Carica papaya L.) fruit flesh and seed growth, fruit respiration, sugar accumulation, and the activities of sucrose phosphate synthase (SPS), sucrose synthase (SS), and acid invertase (AI) were determined from anthesis for ≈150 days after anthesis (DAA), the full ripe stage. Sugar began to accumulate in the fruit flesh between 100 and 140 DAA, after seed maturation had occurred. SPS activity remained low throughout fruit development. The activity of SS was high 14 DAA and decreased to less than one-fourth within 56 DAA, then remained constant during the remainder of fruit development. AI activity was low in young fruit and began to increase 90 DAA and reached a peak more than 10-fold higher, 125 DAA, as sugar accumulated in the flesh. Results suggest that SS and AI are two major enzymes that may determine papaya fruit sink strength in the early and late fruit development phases, respectively. AI activity paralleled sugar accumulation and may be involved in phloem sugar unloading.

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`Chandler' strawberries (Fragaria ananassa Duck.) were kept in air, 0.25% O2, 21% O2 + 50% CO2, or 0.25 O2 + 50% CO2 (balance N2) at 5C for 1 to 7 days to study the effects of controlled atmospheres (CAs) on volatiles and fermentation enzymes. Concentrations of acetaldehyde, ethanol, ethyl acetate, and ethyl butyrate were greatly increased, while concentrations of isopropyl acetate, propyl acetate, and butyl acetate were reduced by the three CA treatments compared to those of air-control fruit. The CA treatments enhanced activities of pyruvate decarboxylase (PDC) and alcohol dehydrogenase (ADH) but slightly decreased activity of alcohol acetyltransferase (AAT). The results indicate that the enhanced PDC and ADH activities by CA treatments cause ethanol accumulation, which in turn drives the biosynthesis of ethyl esters. The increased ethanol concentration also competes with other alcohols for carboxyl groups for esterification reactions. The reduced AAT activity and limited availability of carboxyl groups due to ethanol competition decrease production of other acetate esters.

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Amplified fragment length polymorphisms (AFLPs) were used to analyze the relationships between sweet cherry (Prunus avium L.) cultivars and selections from the breeding program at the Pacific Agri-Food Research Centre in Summerland, Canada. Six pairs of preselected primers were used for the analysis of a total of 67 cultivars and selections. Scoring the absence and presence of 118 polymorphic DNA fragments produced a unique binary code for each cultivar and selection. Two phylogenetic trees were constructed using these 118 polymorphic fragments, one tree for 55 related cultivars and selections from the Summerland breeding program and the other for 23 self-incompatible cultivars of differing origins. The reliability of AFLP DNA fingerprints was confirmed by correlating relationships revealed by AFLP profiles with known genetic relationships of some sweet cherry cultivars and by a blind test for cultivar identification. Results indicate that AFLP analysis is a good technique to evaluate genetic distance and relationships in a sweet cherry breeding population.

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`Hass' avocado (Persea americana Mill.) fruit were kept in air, 0.25% O2 (balance N2), 20 % O2 + 80% CO2, or 0.25% O2 + 80% CO2 (balance N2) at 20C for up to 3 days to study the regulation of fermentative metabolism. The 0.25% 02 and 0.25% 02 + 80% CO2 treatments caused accumulations of acetaldehyde and ethanol and increased NADH concentration, but decreased NAD level. The 20% O2 + 80% CO2 treatment slightly increased acetaldehyde and ethanol concentrations without significant effects on NADH and NAD levels. Lactate accumulated in avocadoes kept in 0.25 % 02. The 80% CO, (added to 0.25% O2) did not increase lactate concentration and negated the 0.25% O2-induced lactate accumulation. Activities of PDC and LDH were slightly enhanced and a new isozyme of ADH was induced by 0.25% O2, 20% O2 + 80% CO2, or 0.25 % O2 + 80% CO2; these treatments partly reduced the overall activity of the PDH complex. Fermentative metabolism can be regulated by changes in levels of PDC, ADH, LDH, and PDH enzymes and/or by metabolic control of the functions of these enzymes through changes in pH, ATP, pyruvate, acetaldehyde, NADH, or NAD. Chemical names used: alcohol dehydrogenase (ADH), adenosine triphosphate (ATP), lactate dehydrogenase (LDH), nicotinamide adenine dinucleotide (NAD), reduced NAD (NADH), pyruvate decarboxylase (PDC), pyruvate dehydrogenase (PDH).

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Papaya (Carica papaya L.) source size and sink strength were modified by a single defoliation or continual defoliation and fruit thinning. Fruit set, development, weight, total sugar (sum of sucrose, fructose, and glucose), sucrose phosphate synthase (SPS), sucrose synthase (SS), and acid invertase (AI) enzyme activities in response to defoliation and fruit thinning were determined. The effects of defoliation and fruit thinning varied with weather conditions, plant growth conditions, and cultivar. Removal of 75% of the leaves significantly reduced new flower production and fruit set, and decreased ripe fruit total soluble solids (TSS), while 50% defoliation did not reduce new fruit set or ripe fruit TSS. When every third leaf from the oldest leaf was not removed, the number of new flowers was reduced by 47% more than when the same number of leaves was removed from the oldest to younger leaves. Continual removal of old leaves reduced new fruit set, fruit weight, and TSS in the 168 day experimental period. Fruit thinning increased new fruit set and ripe fruit TSS. Larger fruit size, faster fruit development, lower respiration rate, and higher sugar contents and AI activity were observed in immature (young) fruit when old fruit were removed. AI activity was reduced during early fruit development and increased again in mature fruit in plants subjected to defoliation, and suggested a role for AI in mature fruit sugar accumulation, while SS activity declined significantly in fruit 154 and 175 days after anthesis and in mature fruit when plants were subjected to continual defoliation. SPS activity was not affected significantly by defoliation or fruit thinning. Source-sink balance was critical for papaya fruit set, development, and sugar accumulation and each mature leaf was able to provide photoassimilate for about three fruit.

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Auxin response factors (ARFs) are an important family of auxin-mediated proteins that have key roles in various physiological and biochemical processes. To the best of our knowledge, no genome-wide identification of the ARF gene family in Arabian jasmine (Jasminum sambac) has been conducted to date. During this study, 24 ARF genes were identified in the Arabian jasmine genome. A phylogenetic analysis suggested that the 24 Arabian jasmine ARFs (JsARFs) were clustered into seven groups and distributed on 11 of the 13 Arabian jasmine chromosomes. The promoter regions of these ARFs were rich in cis-responsive elements related to hormone responses, light responses, and biotic and abiotic stresses. A collinearity analysis showed that certain genes arose by duplication, such as JsARF6 and JsARF19 and JsARF7 and JsARF24. A subsequent analysis of expression profiles based on RNA sequencing data showed that most genes had differential expression patterns among different tissues. The expression levels of 11 genes under indole-3-acetic acid hormone treatment were determined using quantitative real-time polymerase chain reaction, and the results demonstrated that the expression levels of nine JsARF genes were downregulated. Our findings provide valuable information to create the foundation for further functional investigations of the roles of ARF genes in Arabian jasmine growth and development.

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An invertase gene was isolated and its mRNA activity and protein levels were determined during papaya (Carica papaya L.) fruit development. A complete invertase cDNA (AF420223) and a partial sucrose synthase cDNA (AF420224) were isolated from papaya fruit cDNA libraries. The invertase cDNA encoded a predicted polypeptide of 582 residues (MW 65,537 Da), and was 68% and 45% identical with carrot apoplastic and vacuolar invertases, respectively. Key amino acids indicative of an apoplastic invertase were conserved. A full-length gene corresponding to the putative apoplastic invertase cDNA was isolated and was organized into seven exons and six introns. Exon 2 (9 bp long) encoded part of a highly conserved region (NDPNG/A). Invertase mRNA and activity levels increased during fruit maturation and sugar accumulation just before ripening. In contrast, sucrose synthase mRNA levels were high during early fruit growth and low during the fruit sugar accumulation stage. A 73-kDa cell wall extractable protein that cross-reacted with carrot apoplastic invertase antisera substantially increased during papaya fruit maturation and declined in full ripe fruit. The increase in invertase protein levels occurred 2 to 4 weeks before maturity and was markedly higher than the overall increase in enzyme activity at this stage. Subsequently, the increase in enzyme activity was higher than the increase in protein levels between 2 weeks before maturity and fully ripe. The results suggested that mRNA level and invertase activity were related to maturity. The data suggested that the invertase was apoplastic, and that post-translational control of enzyme activity occurred, in which a significant accumulation of invertase occurred before the peak of enzymes activity.

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