低乙烯减压处理对柿果实乙烯生物合成的影响

在 1 0℃± 1℃的条件下 ,研究了低乙烯减压处理对火柿采后乙烯生物合成的影响。结果表明 ,低乙烯减压处理使火柿 ACC含量降低 ,EFE活性减弱 ,从而显著抑制了乙烯的产生 ,延迟了乙烯峰出现的时间。该处理能显著延缓火柿硬度的下降。     

1-甲基环丙烯(1-MCP)对油桃果实软化的影响

1-甲基环丙烯(1-MCP)可延缓油桃果实硬度的下降,阻止引起果实软化的细胞物质(淀粉、纤维素、果胶)的降解,抑制与果实软化相关的酶(淀粉酶、纤维素酶、多聚半乳糖醛酸酶)活性。     

钙对中华猕猴桃果实采后乙烯释放和呼吸的影响

不同浓度ＣａＣｌ２溶液真这渗透处理中华猕猴桃果实采后乙烯释放明显的抑制作用,其中０．５ｍｏｌ／ＬＣａ＾２＋处理尤为显著,采用５天果实人有保持极低水平的内源乙烯,乙烯峰也延迟２－４天出现。     

采后钙处理对荔枝果实过氧化物酶活性,呼吸率及乙烯生成的影响

荔枝果实采后用钙处理,结果表明,适当地提高果实钙含量,可以抑制过氧化物酶的活性,降低呼吸作用及乙烯的生成,达到延缓衰老的目的。本实验以８％钙处理效果最佳。     

采后钙处理对荔枝果实过氧化物酶活性、呼吸率及乙烯生成的影响

荔枝果实采后用钙处理,结果表明,适当地提高果实钙含量,可以抑制过氧化物酶的活性,降低呼吸作用及乙烯的生成,达到延缓衰老的目的。本实验以8％钙处理效果最佳。     

采后钙处理对中华猕猴桃果实过氧化物酶活性、呼吸率及乙烯生成的影响

对中华猕猴桃果实采后进行钙处理,结果表明,适当提高果实钙含量,可以抑制过氧化物酶（POD）活性,降低呼吸率及乙烯生成量,延缓果实衰老。本实验以2％CaCl2处理效果最佳。     

1-MCP对植物乙烯反应的抑制和应用

综述了1-MCP在受体水平上抑制植物对乙烯反应的作用机制,并对其在调控果实,蔬菜和花卉成熟衰老中的潜在应用价值作了介绍。     

GA1处理采后油桃果实膜脂过氧化的影响

采后GA3处理“阿姆肯”油桃果实（Prunus Persica (L.)nectarine.cv.‘armking’),降低了果实中过氧化氢（H2O2）积累和膜脂过氧化产物丙二醛（MDA）含量,显著提高了活性氧清除酶过氧化氢酶（CAT）和抗氧化剂谷胱甘肽（GSH）的含量,降低了果实衰老期间的膜脂过氧化,对“阿姆肯”油桃有一定保鲜效果。     

钙对中华猕猴桃果实采后乙烯释放和呼吸的影响

不同浓度(0.2 mol/L、0.5 mol/L 0.8 mol/L) CaCl₂溶液真空渗透处理对中华猕猴桃果实采后乙烯释放都有明显的抑制作用,其中0.5 mol/L Ca²⁺处理尤为显著,采后5天果实仍保持极低水平的内源乙烯,乙烯峰也延迟2~4天出现。不同品种间没有明显差异。试验结果还表明,Ca²⁺处理对果实采后呼吸不存在明显的抑制作用,但不同品种间有一定差异。     

PRO—LONG涂膜处理对后熟香蕉果实乙烯形成以及其它有关生…

香蕉果实采后以商业上推荐使用的１．５％Ｐｒｏ－ｌｏｎｇ溶液处理,贮藏于２０℃和７５％相对湿度下,分别测定果实的ＡＣＣ含量、ＭＡＣＣ含量、ＥＦＥ酶活性、乙烯释放、叶绿素含量的变化和果实的硬度变化。结果表明,ＰＲＯ－ＬＯＮＧ处理延缓了香蕉果实果皮的叶绿素降解、硬度的下降以及乙烯释放的增加。在后熟过程中,处理果实的ＡＣＣ含量发生积累。ＡＣＣ含量的高峰在乙烯释放高峰和ＥＦＥ酶活性高峰之前出现。与对照比较,     

Responses of strawberry fruit to 1-Methylcyclopropene (1-MCP) and ethylene

1-Methylcyclopropene (1-MCP), a competitive inhibitorof ethylene action, binds to the ethylene receptor toregulate tissue responses to ethylene. In this work,we investigated the effects of 1-MCP and exogenousethylene on ripening, respiration rate, ionicconductivity and peroxidase activity in strawberryfruit. Strawberry fruit can ripen without exogenousethylene treatment, but exogenous ethylene inducessecondary ripening processes. Results indicated thatstimulation of respiration by ethylene wasdose-dependent. Fruit colour development and softeningwere slightly accelerated by ethylene, but changes insoluble solid content were not. 1-MCP may/may notaffect the respiratory rise induced by exogenousethylene dependent on fruit maturity. Cycloheximide(CHI) reduced the ethylene-induced respiratoryincrease. Combinations of 1-MCP and CHI reducedrespiration more than CHI alone. 1-MCP and CHI did notinfluence the primary respiratory change in nonethylene-treated fruit. This indicates that ethyleneinduced respiratory increase may involve an ethylenereceptor in early harvested fruit, but not in laterharvested fruit. Exogenous ethylene stimulatedrespiration by regulating new respiratory enzyme(s)synthesis in strawberry fruit. Ethylene induced anionic leakage increase, and this was positivelycorrelated to fruit water loss and peroxidaseactivity. These results suggest that non-climactericfruit, such as strawberry, may have different ethylenereceptor(s) and/or ethylene receptor(s) may havedifferent regulatory functions. It may be thesecondary effect of ethylene to stimulate respirationin strawberry. Non-climacteric fruit ripening may berelated to the development of active oxygen species(AOS) induced by postharvest stress.     

大棚油桃授粉方式研究初报

2002年2-5月,研究利用蜜蜂、壁蜂花期传粉及人工授粉技术对大棚油桃艳光和潍甜1号的座果率及产量均有不同程度的提高;其中潍甜1号的座果率提高幅度最大。上述几种方法中,人工授粉的效果最好。     

Carbon dioxide and 1-MCP inhibit ethylene production and respiration of pear fruit by different mechanisms

Ethylene production in relation to O2 partial pressure of whole pear fruit stored at 2C could be described by a Michaelis-Menten equation. This was indicated by the use of a gas exchange model. The maximum ethylene production rate was strongly inhibited while the KmO2 value (1.25 kPa) was not affected by elevated CO2. Ethylene production was also inhibited by 1-MCP, an inhibitor of ethylene perception. The reduction in ethylene production by CO2 was similar for 1-MCP treated and untreated pears. Elevated CO2, therefore, must have had an influence on ethylene production other than through ethylene perception. A possible site of inhibition by CO2 is the conversion of ACC to ethylene. The O2 uptake rate in relation to O2 partial pressure of whole pear fruit could be described by a Michaelis-Menten equation. The O2 uptake rate was inhibited by elevated CO2 at a level similar to the inhibition of ethylene production. Again the KmO2 value (0.68 kPa) was not affected by CO2. Using 1-MCP treatments it was shown that there was no direct effect of inhibited ethylene production on O2 uptake rate.     

Effects of 1-MCP and exogenous ethylene on fruit ripening and antioxidants in stored mango

Mango (Mangifera indica L. cv. Tainong) fruits were harvested at the green-mature stage in Hainan and air-freighted to the laboratory at Peking. The fruits were treated with either 1 μl l⁻¹ 1-MCP or 5 μl l⁻¹ ethylene for 24 h and stored at 20°C for up to 16 days. 1-MCP maintained fruit firmness, whereas exogenous ethylene decreased fruit firmness. Exogenous ethylene accelerated the increase in ethylene and 1-aminocyclopropane-1-carboxylate (ACC) oxidase, whereas 1-MCP reduced both. Exogenous ethylene stimulated and 1-MCP inhibited the production of H₂O₂ of mango fruit during storage. Ascorbic acid was maintained at a high concentration in 1-MCP-treated fruit but was low in ethylene-treated fruit. 1-MCP inhibited activities of antioxidant enzymes including catalase, superoxide dismutase and ascorbate peroxidase. These results suggest that 1-MCP could play a positive role in regulating the activated oxygen metabolism balance. Baogang Wang and Jianhui Wang contributed equally to this work.     

CEPA处理对苦瓜采后呼吸、乙烯释放及保护系统的影响

CEPA处理适期采收的食用苦瓜后,使其呼吸速率,乙烯释放速率明显增加,呼吸上升、瓜皮转黄期由采后第8天提前至第6天,且使贮期缩短4d。CEPA处理不同程度地抑制了苦瓜采后前期的各种保护酶活性,且使衰老后期的保护酶活性上升期提前。CEPA处理后前6d,AsA、GSH含量均呈上升趋势;6d后迅速下降,且下降速率大于CK。CEPA处理未改变苦瓜采后MDA含量总体下降的趋势。     

Effects of anaerobiosis on ethylene production, respiration and flowering in iris bulbs

Ethylene production of iris bulbs (Iris hollandica cv. Ideal) was very low. When stored at 30°C, production was 12–20 pmol C₂H₄ (kg fresh weight)^?1 h^?1. Higher temperatures (35°C, 40°C) enhanced the ethylene production; a treatment with 40°C for ca 7 days caused a 3 times higher ethylene production than at 30°. During anaerobic storage (in 100% N₂) ethylene production was equal to that of control bulbs. When after a 7 day period of anaerobiosis the N₂ was replaced by air, a burstlike ethylene production was observed. Twenty-four h after the replacement, ethylene production was equal to control values again. The effects of this production of ethylene on mitochondrial respiration and flowering were investigated. When mitochondria were isolated immediately after the anaerobic treatment (before the enhanced ethylene production) alternative pathway capacity was not detectable, a situation also occurring in control bulbs. When mitochondria were isolated 24 h after the end of the anaerobiosis (after the ethylene burst) uninhibited respiration did not change significantly, but a capacity of the alternative pathway was observed. The increase in alternative pathway capacity after anaerobiosis was partly inhibited by 2,5-norbornadiene (NBD), an ethylene antagonist. Fermentation occurred during anaerobiosis: ethanol concentrations increased during the treatment and decreased when air was supplied. When bulbs were exposed to ethanol vapour the alternative pathway was induced but only when very high ethanol levels in the bulbs were reached. The amount of ethanol accumulated in the bulbs during a 7 day anaerobic treatment was far too low to explain the observed induction of alternative pathway capacity. Flowering percentages were enhanced after a 24 h treatment with ethylene and after a 7 day anaerobic treatment. NBD significantly inhibited the effect of exogenous ethylene and of anaerobiosis on flowering. Ethanol was not able to induce flowering. The burst-like production of ethylene after anaerobiosis probably is responsible for the effects on respiration and flowering.     

Inhibition of wound ethylene in Lycopersicum esculentum fruit discs by 1-amino cyclopropane-1-carboxylic acid oxidase inhibitors

Inhibition of wound-ethylene by eight structural analogues of 1-aminocyclopropane-1-carboxylic acid (ACC) studied seperately was investigated in unripe tomato fruit discs (Lycopersicum esculentum). The compounds tested were: trans-2-phenylcyclopropane-1-carboxylic acid (PCCA), cyclopropane-1,1-dicarboxylic acid (CDA), cyclopropylamine (CPA), cyclopropyl methyl ketone (CMK), chrysanthemyl alcohol (CHRA), 2-methyl cyclopropanecarboxylic acid (MCA), cyclopropanecarboxylic acid (CCA), 2-methyl-cyclopropane-methanol (2-MCM). The level of inhibition was a function of treatment concentration and time. Differential inhibition induced by the tested compounds was related to their structure.     

成串采收对番茄果实采后乙烯合成及贮藏品质的影响

为研究成串采收对番茄果实采后乙烯合成及贮藏品质的影响,对广西田阳县两个栽培区两种嫁接砧木的串收番茄的采后生理指标进行测定,探讨了该采收方式对番茄果实采后保鲜的作用机制。结果表明:整个贮藏期,不同栽培区不同嫁接砧木的番茄成串采收的果实,乙烯生成量明显低于对照的常规单果采收。其中,砧木1号Ⅰ区的串收番茄的乙烯生成量,采后5 d即下降至最低点(0.35 nL·g~(-1)·h~(-1)),显著低于其对照(1.36 nL·g~(-1)·h~(-1)),其他栽培区和砧木组合的串收番茄,在采后15 d乙烯生成量达到最低值。串收番茄的类胡萝卜素、番茄红素和抗坏血酸等果实内天然抗氧化物质的含量,在贮藏前期快速升高,且峰值显著高于对照。此外,成串采收处理还一定程度抑制了果实后熟阶段可溶性糖的积累和可滴定酸的分解。因此,番茄成串采收处理,可能通过抑制果实采后乙烯的合成,同时提高类胡萝卜素、番茄红素和抗坏血酸的水平,并且推迟糖和酸等营养物质的后熟变化进程,实现其延长果实货架期,提高商品品质的作用。     

Subcellular localization of the sites of conversion of 1-aminocyclopropane-1-carboxylic acid into ethylene in plant cells

The subcellular localization of the sites of 1-aminocyclopropane-1-carboxylic acid (ACC) conversion into ethylene was studied by comparing the specific radioactivity of ethylene evolved from the whole cells with that of intra- and extracellular pools of labelled ACC. We demonstrate that some cells cultured in vitro (Vitis vinifera L. cv. Muscat) or leaf tissues (Hordeum vulgare L. and Triticum aestivum L.) have two sites of ethylene production: (i) an external site, converting apoplastic ACC, located at the plasma membrane, and very sensitive to high osmotica and, (ii) an intracellular site, converting internal ACC and remaining unaffected even under severe plasmolysis. In other cells cultured in vitro (Vitis vinifera L. cv. Gamay) and pea leaves (Pisum sativum L.), only the intracellular site operates and ethylene production is almost unaffected by plasmolysis. Protoplasts obtained from plasmolysis-sensitive Muscat cells lose 97% of their capacity for ethylene production compared with the parent cell, while those from plasmolysisinsensitive Gamay cells retain up to 50%. Protoplasts from both Gamay and Muscat cells cultured for 8 d in vitro, recover the full capacity of ethylene production of the initial whole cells, whether or not they are allowed to reform their cell wall. Therefore, we exclude a cooperation between the cell wall and the plasma membrane in ethylene production.Abbreviations ACC 1-aminocyclopropane-1-carboxylic acid - EFE ethylene-forming enzyme We are grateful to Dr. Philip John (Reading, UK) for useful discus sions made possible by a North Atlantic Treaty Organization Colla borative Grant (No. 0383/88) and Dr. Yves Meyer (Perpignan, France) for his collaboration in culturing protoplasts.