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小麦幼苗响应冷胁迫和热胁迫的早期和晚期质体发育。

Early and late plastid development in response to chill stress and heat stress in wheat seedlings.

机构信息

School of Life Sciences, Jawaharlal Nehru University, New Delhi, 110 067, India.

出版信息

Protoplasma. 2011 Oct;248(4):725-36. doi: 10.1007/s00709-010-0235-4. Epub 2010 Nov 10.

Abstract

Five-day-old etiolated wheat (Triticum aestivum L.) seedlings were transferred to 7°C (chill stress), 25°C (control), and 42°C (heat stress) and were kept in the dark or light for different time periods. Plastids were isolated from the control and stressed seedlings, and their low-temperature (77 K) fluorescence emission spectra were monitored. Most of the Protochlorophyllide (Pchlide) present in heat-stressed etiolated seedlings were in nonphototransformable form. The phototransformable Pchlide (F657) rapidly decreased when 5-day-old etiolated seedlings were transferred to 42°C in the dark for 24 h. A flash illumination of 0.2 s given to etiolated heat-stressed seedlings resulted in substantial arrest of Shibata shift, while in chill-stress conditions, it was only partially affected. In high temperature, due to disaggregation of polymeric Pchlide-Pchlide oxidoreductase (POR)-nicotinamide adenine dinucleotide phosphate (NADPH) molecules, the conversion of nonphototransformable Pchlide to its phototransformable form is substantially delayed resulting in impaired Shibata shift and belated development of the core antenna CP47 Photosystem II (PSII). Chill stress, however, did not disaggregate the polymeric Pchlide-POR-NADPH molecule-suppressed Pchlide and Chl synthesis and impaired of the assembly of PSII core antenna CP47 that emits F695 and PSI that emits F735. The decreased gene/protein expression and reduced posttranslational import of plastidic proteins, importantly POR in temperature-stressed plants, may be responsible for the delay in conversion of nonphototransformable to phototransformable form of Pchlide and plastid biogenesis.

摘要

将 5 天大的黄化小麦(Triticum aestivum L.)幼苗转移到 7°C(冷胁迫)、25°C(对照)和 42°C(热胁迫),并在黑暗或光照下保持不同时间。从对照和胁迫的幼苗中分离出质体,并监测其低温(77 K)荧光发射光谱。热胁迫下黄化幼苗中存在的大多数原叶绿素(Pchlide)处于不可光转化形式。当 5 天大的黄化幼苗在黑暗中转移到 42°C 24 小时时,可光转化的 Pchlide(F657)迅速减少。对黄化热胁迫幼苗进行 0.2 s 的闪光照射会导致 Shibata 移位大量停止,而在冷胁迫条件下,仅部分受到影响。在高温下,由于聚合的 Pchlide-Pchlide 氧化还原酶(POR)-烟酰胺腺嘌呤二核苷酸磷酸(NADPH)分子的解聚,不可光转化的 Pchlide 向其可光转化形式的转化被大大延迟,导致 Shibata 移位受损和核心天线 CP47 光系统 II(PSII)的延迟发育。然而,冷胁迫不会解聚聚合的 Pchlide-POR-NADPH 分子抑制的 Pchlide 和 Chl 合成,并损害 PSII 核心天线 CP47 的组装,该天线发射 F695 和 PSI 发射 F735。基因/蛋白表达减少和质体蛋白的翻译后导入减少,尤其是在温度胁迫下的植物中 POR,可能是导致 Pchlide 从不可光转化形式向可光转化形式的转化延迟和质体生物发生的原因。

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