柑橘精油及壳聚糖复合处理对橄榄果实采后生理和耐贮性的影响

为探究柑橘精油(0.25%、0.75%、1.5%)和壳聚糖(0.25%、0.75%、1.5%)复合处理对橄榄(Canarium album)果实采后生理和耐贮性的影响，以鲜食橄榄品种(系)‘檀香’、‘梅埔2号’为材料，对采后贮藏期间的腐烂率、褐变指数、相对电导率、呼吸强度、丙二醛含量、内源抗氧化物质谷胱甘肽含量、过氧化物酶(POD)、抗坏血酸过氧化物酶(APX)活性进行测定，筛选橄榄果实复合保鲜剂的最佳浓度组合。结果表明，与对照相比，所有柑橘精油和壳聚糖复合处理均可有效降低橄榄果实在贮藏期间腐烂率、褐变指数和丙二醛的积累，抑制呼吸作用，保持较高的内源抗氧化物质谷胱甘肽含量和POD、APX活性。因此柑橘精油及壳聚糖处理能够有效延长橄榄果实的保鲜时间，提高耐贮性，其中以1.5%柑橘精油和1.5%壳聚糖组合的保鲜效果最佳。     

奉节脐橙果实苯丙氨酸解氨酶活性及其基因表达与果皮褐变的关系

柑橘果皮褐变严重影响果实的商品价值和耐贮性．以奉节脐橙（Citrus sinensis Osbcck）果实为材料,通过采后常温、涂蜡、低温、机械损伤等处理研究了果实果皮褐变率、苯丙氨酸解氨酶（PAL）活性及PAL上基因在果皮褐变过程中表达水平的变化。结果表明,涂蜡、损伤处理均极显著地提高果实的果皮褐变率,而低温贮藏可显著降低其发生率;贮藏期问各处理的PAL活性均呈上升趋势,损伤处理PAL活性显著高于对照。果实发生褐变或受到机械损伤后,PAL2、PAL6基因的表达均比对照明显增强。结果首次表明脐橙果实PAL活性变化以及PAL2基因的表达与果皮褐变具有非常密切的关系．     

臭氧与海藻酸钠涂膜对葡萄的保鲜效果及其贮藏生理特性的影响

以采后"红地球"葡萄果实为试材,分别设置对照(CK)、250μL/L臭氧处理(O3)、0.3%海藻酸钠涂膜处理(M)、250μL/L臭氧+0.3%海藻酸钠涂膜处理(O3+M),在(0±0.5)℃条件下贮藏,通过测定贮藏过程中葡萄可溶性固形物含量、可滴定酸含量、呼吸强度、硬度、过氧化物酶(POD)、超氧化物歧化酶(SOD)、几丁质酶(CHI)、β-1,3-葡聚糖酶(GLU)的活性以及膜脂过氧化物质丙二醛(MDA)和总酚含量等的变化,统计果实失重率与腐烂率情况,观察各处理对葡萄保藏效果的影响。结果表明:与对照相比,250μL/L臭氧处理、0.3%海藻酸钠涂膜及250μL/L臭氧+0.3%海藻酸钠涂膜复合处理均能显著降低葡萄果实的失重率和腐烂率,抑制葡萄果实的呼吸上升,延缓硬度下降,提高果实抗性相关酶(POD、SOD、GLU、CHI)的活性,减少膜脂的过氧化程度,延缓果实总酚含量下降,有效改善葡萄的贮藏品质,并以250μL/L臭氧+0.3%海藻酸钠涂膜复合处理对葡萄果实保鲜效果最佳。     

壳聚糖涂膜对杨梅品质的影响（简报）

1％壳聚糖涂膜可降低杨梅果实呼吸速率,保持果肉硬度,延缓总酸和总糖含量的下降以及还原糖的上长,贮藏16d仍然具有较高的商品价值。     

钙处理对红富士苹果酶促褐变的影响

渗钙处理能够明显保持红富士苹果的硬度,且褐变度明显低于对照,渗钙对酶促褐变的抑制作用是通过影响PPO活性和LOX活性起作用的,果实褐变的早期发动与LOX活性相关密切,后期褐变则主要是PPO起作用。     

壳聚糖涂膜对番荔枝冷藏期间某些生理生化指标的影响

经1％壳聚糖涂膜处理的番荔枝果实在冷藏（15℃）期间可溶性固形物（TSS）含量变化过程延缓,果实腐烂率显著降低,超氧化物歧化酶（SOD）和过氧化物酶（POD）活性提高,多酚氧化酶（PPO）活性和丙二醛（MDA）含量下降,过氧化氢酶（CAT）活性变化不明显。     

O2和CO2配比对气调贮藏梨采后褐变及相关理化因子的影响

以采后'丰水'梨果实为材料,在乐扣气调试验箱中研究了O2和CO2配比对果实褐变率、多酚氧化酶(PPO)和过氧化物酶(POD)活性、丙二醛(MDA)和总酚含量的影响,以探讨适宜减轻梨气藏褐变的气体成份.结果表明:在整个贮藏过程(150 d)中,'丰水'梨果肉未发生褐变.从贮藏60 d开始,气调处理和冷藏对照果实的果皮均出现褐变,气调处理在贮藏120 d之前对果皮褐变的影响不显著,而在贮藏120～150 d内可显著减轻果皮的褐变、抑制果皮PPO和POD活性及降低总酚含量.与冷藏对照相比,气调处理可推迟果心褐变的时间,且(8%～10%)O2+3% CO2处理可完全抑制果心的褐变;气调处理亦可降低果心PPO活性、减少总酚及MDA含量;(8%～10%)O2+1% CO2处理能够显著提高果心的POD活性,而(8%～10%)O2+3% CO2处理对果实POD活性的影响不显著.可见,气调贮藏主要是通过降低'丰水'梨果皮PPO、POD活性及总酚含量来减轻组织的褐变,并以(8%～10%)O2+3% CO2处理对果实褐变因子的控制效果较理想.     

1-MCP和CO2对‘南果梨’冷藏后货架期能量代谢特性的影响

分别对‘南果梨’果实采用0.75μL/L 1-甲基环丙烯(1-MCP)在20℃熏蒸20h后装入保鲜袋(0.02mm)、用2%CO2充气果实包装袋(0.04mm)、以保鲜袋果实为对照,各处理组果实均置于(0±1)℃贮藏5个月后移至室温下(18℃±3℃),测定各处理果实在货架期间的褐变度以及果实线粒体蛋白含量、MDA含量、ATP含量,以明确1-MCP和CO2对南果梨冷藏后果实货架期的能量代谢特性。结果显示:(1)1-MCP和CO2处理可不同程度延缓南果梨冷藏后货架期果实果心褐变指数和褐变度,且1-MCP处理效果更好,但CO2处理在货架后期反而使果实褐变度较对照提高。(2)1-MCP和CO2处理可有效抑制果实MDA含量增加,延缓细胞膜透性的升高,保持细胞完整性。(3)1-MCP处理有利于提高货架前期果实中线粒体蛋白质含量,能够在货架后期保持较高的ATP含量和能荷水平,而CO2处理在货架前期果实内含有较高水平的ATP,促进了果实内的能荷水平。研究发现,1-MCP和CO2处理均可以通过影响南果梨果实的能量代谢特性从而影响果实的成熟衰老进程,且1-MCP处理可以抑制货架前期的ATP含量和能量供应,有利于保持细胞膜完整性,抑制果心褐变的发生,延缓果实成熟衰老进程;而2%CO2处理与对照相比对果实能量代谢特性的影响不大。     

壳聚糖涂膜对苹果的保鲜效应（简报）

经1％壳聚糖涂膜的国光苹果,在室温下贮藏5个月后,果实保持绿色,有光泽,无皱缩;果实吸氧弱,呼吸速率降低,呼吸高峰延迟,磷酸戊糖途径升高;体内活性氧形成量减少,膜脂过氧化降低,细胞膜损伤得到缓解;细胞内不溶性钙有提高,可溶性钙下降,活性的CaM也减少,因而膜脂分解减缓。     

采后枸杞鲜果褐变与其活性氧代谢的关系

以采后'宁杞3号'枸杞鲜果为试材,研究其在(4±1)℃和(10±1)℃贮藏过程中果实褐变与活性氧代谢的关系.结果表明:枸杞果实褐变指数在两种贮藏温度下的贮藏初期(0～10 d)增加幅度均较小(分别为17.6%和5.1%),(10±1)℃下的果实从第15天显著增大(64.1%),而(4±1)℃下从第20天显著增大(67.9%).(4±1)℃贮藏果实的超氧歧化酶(SOD)活性和还原型抗坏血酸(AsA)含量在采后贮藏的前10 d增大,之后降低,贮藏后期又增大;超氧阴离子(O2-)产量在采后0～5 d降低,而后逐渐增大;过氧化氢(H2O2)和丙二醛(MDA)含量在采后0～5 d增大.之后前者降低又缓慢升高.与(10±1)℃贮藏果实相比,(4±1)℃下贮藏果实O2-产量显著降低,H2O2含量在贮藏第5天和第25天也显著降低,MDA含量在贮藏5～20 d显著降低;SOD活性在贮藏5～10 d显著提高.过氧化氢酶(cAT)活性和AsA含量明显提高;多酚氧化酶(PPO)活性在贮藏15～25 d显著下降,总酚含量在贮藏5～20 d显著增加.研究发现,枸杞果实褐变可能是细胞活性氧代谢失调,使PPO与酚类物质接触,导致酚类物质氧化的结果;(4±1)℃低温贮藏能通过调整鲜果活性氧代谢来有效延缓褐变进程.     

5种新疆苹果资源的果实品质性状比较与评价

选择5种果皮和果肉颜色不同的新疆苹果地方特色资源克孜阿尔玛、卡拉阿尔玛、阿克阿尔玛、伊犁野苹果、柠檬海棠,以栽培品种富士为对照,通过果实外观品质、内在品质、营养品质和香气品质4个方面的指标进行品质精细化评价,并考察了红肉苹果果肉花青苷合成途径相关基因的表达情况,以明确新疆苹果地方资源不同果实品质指标的差异,为新疆苹果地方资源的合理利用提供资料。结果表明:(1)5种特色资源均为中、小果型苹果,其中红肉品种克孜阿尔玛的外观品质优于栽培品种富士,而柠檬海棠外观品质指标均处于最低水平。(2)阿克阿尔玛的糖、酸含量均显著低于富士,柠檬海棠的酸含量高于富士及其他品种。(3)伊犁野苹果的果肉硬度显著高于富士,而红肉资源品种的果肉硬度均低于富士,肉质松软、不耐储运,但其总酚、类黄酮含量最为丰富,抗氧化能力最强,均显著高于栽培品种富士。(4)香气品质中,红皮资源卡拉阿尔玛的挥发性物质种类及含量最为丰富,其含量高于最低的栽培品种富士近2倍,红肉资源的挥发性物质含量最低;红肉资源的挥发性物质以醇类为主,而红皮资源卡拉阿尔玛、伊犁野苹果和柠檬海棠以醛类物质为主。(5)主成分分析显示,各个新疆苹果地方资源营养、香气品质等综合品质表现为:克孜阿尔玛卡拉阿尔玛阿克阿尔玛富士伊犁野苹果柠檬海棠。(6)红肉苹果的果肉花青苷合成途径相关基因表达分析表明,其果肉花青苷积累过程中的关键基因是UFGT。     

A Multidisciplinary Approach Providing New Insight into Fruit Flesh Browning Physiology in Apple (Malus x domestica Borkh.)

In terms of the quality of minimally processed fruit, flesh browning is fundamentally important in the development of an aesthetically unpleasant appearance, with consequent off-flavours. The development of browning depends on the enzymatic action of the polyphenol oxidase (PPO). In the ‘Golden Delicious’ apple genome ten PPO genes were initially identified and located on three main chromosomes (2, 5 and 10). Of these genes, one element in particular, here called Md-PPO, located on chromosome 10, was further investigated and genetically mapped in two apple progenies (‘Fuji x Pink Lady’ and ‘Golden Delicious x Braeburn’). Both linkage maps, made up of 481 and 608 markers respectively, were then employed to find QTL regions associated with fruit flesh browning, allowing the detection of 25 QTLs related to several browning parameters. These were distributed over six linkage groups with LOD values spanning from 3.08 to 4.99 and showed a rate of phenotypic variance from 26.1 to 38.6%. Anchoring of these intervals to the apple genome led to the identification of several genes involved in polyphenol synthesis and cell wall metabolism. Finally, the expression profile of two specific candidate genes, up and downstream of the polyphenolic pathway, namely phenylalanine ammonia lyase (PAL) and polyphenol oxidase (PPO), provided insight into flesh browning physiology. Md-PPO was further analyzed and two haplotypes were characterised and associated with fruit flesh browning in apple.     

Metabolic changes in 1-methylcyclopropene (1-MCP)-treated ‘Empire’ apple fruit during storage

??Empire?? apple fruit are more susceptible to flesh browning at 3.3°C if treated with 1-methylcyclopropene (1-MCP), an inhibitor of ethylene perception. To better understand the metabolic changes associated with this browning, untargeted metabolic profiling with partial least squares analysis has been used to visualize changes in metabolic profile during hypoxic controlled atmosphere (CA) storage, ethylene insensitivity, and disorder development. Overall, most carbohydrates and organic acids were not appreciably affected, but the levels of amino acids and volatile metabolites were significantly affected, by 1-MCP treatment. Sorbitol and levels of some amino acids were elevated towards the end of storage in 1-MCP treated fruit. CA storage reduced the levels of many volatile components and 1-MCP reduced these levels further. Additionally multiple metabolites were associated with the development of flesh browning symptoms. Unlike other volatile compounds, methanol levels gradually increased with storage duration, regardless of 1-MCP treatment, while 1-MCP decreased ethanol production. Results reveal metabolic changes during storage that may be associated with development of flesh browning symptoms.     

自然贮存苹果的生化分析及形态解剖学研究

本文对自然贮存六个月的秦冠、红富士及新红星苹果果实在生化成分及显微、超微结构上进行了对比研究,发现红富士果实中果胶质、总糖及粗蛋白含量均高于其它品种;三种果实表面均有不同形态的蜡质分布;果皮角化层以红富士较厚,新红星次之;不同品种果肉细胞的形态有明显差异。本文对此结果进行了初步的探讨,以期为苹果贮存研究积累资料。     

The phenylpropanoid pathway affects apple fruit resistance to Botrytis cinerea

Apple fruits are rich in phenolic compounds that may enhance resistance to grey mould disease caused by Botrytis cinerea. Using Malus domestica Borkh. cultivars Fuji and Qinguan, we analysed the contents of total phenols, total flavonoids, eight individual phenolic compounds, H₂O₂ and O₂^.? as well as the activities of key enzymes in the phenylpropanoid pathway in the flesh of control and B. cinerea‐inoculated fruits. Chlorogenic acid contents increased for a short period in the less susceptible cultivar Qinguan fruits, but decreased in the disease‐susceptible Fuji fruits. Additionally, ferulic acid production was induced in both cultivars in response to B. cinerea. Furthermore, the activities of phenylalanine ammonia lyase, cinnamate 4‐hydroxylase, 4‐coumarate:coenzyme A ligase and cinnamyl alcohol dehydrogenase were differentially induced between the two apple cultivars. Remarkably, the contents of H₂O₂ and O₂^.? as well as the activities of enzymes in phenolic metabolism tested in this study were always higher in Qinguan fruits than in Fuji fruits. Our data imply that phenylpropanoid metabolism is closely associated with apple fruit resistance to grey mould disease. These findings may be useful for characterizing the mechanism(s) underlying plant resistance to B. cinerea, with potential implications for the screening of grey mould disease‐resistant apple varieties in breeding programmes.     

Lipoxygenase activity in apples in relation to storage and physiological disorders

Different methods for the preparation of active lipoxygenase (LOX) extracts from apples were compared. Highest activities were obtained using a 0.25 M phosphate buffer (pH 7) containing 1% Triton X-100 and 10^?2 M metabisulphite as extraction solvent. LOX activity during storage was investigated in the core, flesh, and peel. Activity was always highest in the core and peel. On storage, activity was increased in each part of the fruit but especially in the core and peel. Increase in LOX preceded the browning of the core. LOX may be responsible for the browning and may be concerned in the induction of superficial scald.     

转录组和代谢组联合解析苹果采后高浓度CO2伤害机制

环境气体浓度影响果蔬的贮藏保鲜期和品质,高浓度CO2长时间处理会造成果实的伤害,但具体的分子机制不清楚。本研究以高浓度CO2处理采后富士苹果为材料,利用Illumina Hiseq 4000高通量测序技术和非靶向代谢技术分别对苹果内部褐变果肉组织和对照组正常果肉组织进行转录组测序和代谢组学分析,解析苹果CO2伤害产生的机制。结果如下：转录组测序共获得6 332个差异基因,包括4 187个上调基因和2 145个下调基因。差异基因进行功能性分析初步确定苹果CO2伤害的发生与氧化还原过程、脂类代谢、激素信号转导过程、能量代谢过程有关,并成功筛选出20个候选褐变基因,其中grxcr1 (MD14G1137800)、gpx (MD06G1081300) 参与活性氧清除过程,pld1_2 (MD15G1125000) 和plcd (MD07G1221900) 参与磷脂酸合成,影响膜代谢,mdh1 (MD05G1238800) 参与TCA循环,影响能量代谢。代谢组分析共获得77个差异代谢物,主要是有机酸、脂类、糖类和多酮类化合物,其中包括35个与褐变相关的代谢物质。将差异基因和差异代谢物进行联合分析,结果显示,类黄酮生物代谢过程参与了苹果的褐变过程,褐变组织与对照组织比较发现儿茶素、槲皮素等黄酮类含量明显下降,细胞抗氧化能力下降,氧化还原状态失衡,细胞结构破坏,造成褐变。本研究结果进一步丰富了CO2伤害产生的理论基础,同时为高浓度CO2保鲜技术的实际应用提供理论指导。     

龙眼果实采后失水果皮褐变与活性氧及酚类代谢的关系

研究了(10±1)℃和50%相对湿度贮藏条件下"福眼"龙眼果实果皮褐变与活性氧和酚类代谢的关系.结果表明,采后失水导致龙眼果实果皮褐变,果皮活性氧清除酶SOD、CAT、APX、GR活性和内源抗氧化物质AsA、GSH含量下降,O-2产生速率和MDA含量增加,细胞膜透性迅速增大;PPO和POD活性增加,总酚和类黄酮含量明显下降.据此认为,果皮褐变可能是细胞的活性氧代谢失调,细胞膜结构破坏,使PPO、POD与酚类物质(含类黄酮)接触、酚类物质氧化的结果.