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Divinyl Chlorophyll(ide) a Can Be Converted to Monovinyl Chlorophyll(ide) a by a Divinyl Reductase in Rice

机译:水稻中的二乙烯基还原酶可以将二乙烯基叶绿素(a)转化为单乙烯基叶绿素(a)

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摘要

3,8-Divinyl (proto)chlorophyll(ide) a 8-vinyl reductase (DVR) catalyzes the reduction of 8-vinyl group on the tetrapyrrole to an ethyl group, which is indispensable for monovinyl chlorophyll (Chl) synthesis. So far, three 8-vinyl reductase genes (DVR, bciA, and slr1923) have been characterized from Arabidopsis (Arabidopsis thaliana), Chlorobium tepidum, and Synechocystis sp. PCC6803. However, no 8-vinyl reductase gene has yet been identified in monocotyledonous plants. In this study, we isolated a spontaneous mutant, 824ys, in rice (Oryza sativa). The mutant exhibited a yellow-green leaf phenotype, reduced Chl level, arrested chloroplast development, and retarded growth rate. The phenotype of the 824ys mutant was caused by a recessive mutation in a nuclear gene on the short arm of rice chromosome 3. Map-based cloning of this mutant resulted in the identification of a gene (Os03g22780) showing sequence similarity with the Arabidopsis DVR gene (AT5G18660). In the 824ys mutant, nine nucleotides were deleted at residues 952 to 960 in the open reading frame, resulting in a deletion of three amino acid residues in the encoded product. High-performance liquid chromatography analysis of Chls indicated the mutant accumulates only divinyl Chl a and b. A recombinant protein encoded by Os03g22780 was expressed in Escherichia coli and found to catalyze the conversion of divinyl chlorophyll(ide) a to monovinyl chlorophyll(ide) a. Therefore, it has been confirmed that Os03g22780, renamed as OsDVR, encodes a functional DVR in rice. Based upon these results, we succeeded to identify an 8-vinyl reductase gene in monocotyledonous plants and, more importantly, confirmed the DVR activity to convert divinyl Chl a to monovinyl Chl a.
机译:3,8-二乙烯基(原)叶绿素(ide)8-乙烯基还原酶(DVR)催化将四吡咯上的8-乙烯基还原为乙基,这对于单乙烯基叶绿素(Chl)的合成是必不可少的。到目前为止,已经从拟南芥(Arabidopsis thaliana),拟南芥(Chlorobium tepidum)和Syechocystis sp。中鉴定了三个8-乙烯基还原酶基因(DVR,bciA和slr1923)。 PCC6803。但是,尚未在单子叶植物中鉴定出8-乙烯基还原酶基因。在这项研究中,我们在水稻(Oryza sativa)中分离了一个自发突变体824ys。该突变体表现出黄绿色的叶子表型,降低了Chl水平,阻止了叶绿体发育,并阻碍了生长速度。 824ys突变体的表型是由水稻染色体3短臂上的一个核基因的隐性突变引起的。基于图谱的克隆此突变体导致鉴定出一个基因(Os03g22780),该基因与拟南芥DVR基因具有序列相似性(AT5G18660)。在824ys突变体中,在开放阅读框的952-960位残基上缺失了9个核苷酸,导致编码产物中3个氨基酸残基的缺失。 Chls的高效液相色谱分析表明,该突变体仅积累了二乙烯基Chl a和b。由 Os03g22780 编码的重组蛋白在大肠杆菌中表达,并发现其催化二乙烯基叶绿素(ide) a 向单乙烯基叶绿素(ide)的转化) a。因此,已经证实,重命名为 OsDVR Os03g22780 可编码水稻中的功能性DVR。基于这些结果,我们成功地鉴定了单子叶植物中的8-乙烯基还原酶基因,更重要的是,证实了DVR活性可将二乙烯基Chl a 转化为单乙烯基Chl a

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