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首页> 外文期刊>Plant Molecular Biology >Arrest of chlorophyll synthesis and differential decrease of Photosystems I and II in a cyanobacterial mutant lacking light-independent protochlorophyllide reductase
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Arrest of chlorophyll synthesis and differential decrease of Photosystems I and II in a cyanobacterial mutant lacking light-independent protochlorophyllide reductase

机译:缺乏光非依赖性原叶绿素还原酶的蓝藻突变体中叶绿素合成的逮捕和光系统I和II的差异减少

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The chlL gene encodes one subunit of the light-independent protochlorophyllide reductase. A chIL-lacking mutant of the cyanobacterium Plectonema boryanum is unable to synthesize chlorophyll (Chl) in the dark, causing Chl synthesis to become light-dependent as in angiosperms. When the mutant cells were cultivated heterotrophic ally in the dark, Chl synthesis was arrested and the Chl content decreased exponentially in reverse profile to cell propagation, indicating that most of the pre-existing Chl was recruited for daughter cells. During this 'etiolating' process the Chl content became less than 0.5% of the original level. In parallel to this there was a decrease in the activity of Photosystem I (PSI), the amount of its core Chl-binding subunits, PsaA/PsaB, and a peripheral subunit, PsaC. Levels of transcripts for these subunits were not significantly changed upon the arrest of Chl synthesis. In contrast, Photosystem II (PSII) was maintained to a significant extent in terms of activity and protein levels of D1 and CP47 until a late stage of the etiolation, implying that PSII is newly synthesized though Chl synthesis was arrested. Low-temperature (77 K) fluorescence spectral analysis supported a selective decrease in Chl associated with PSI. Taken together, it is suggested that the pre-existing Chl molecules in periphery of PSI could be released and re-distributed for PSII biosynthesis in the etiolating cyanobacterial cells. [References: 48]
机译:chlL基因编码光独立的原叶绿素还原酶的一个亚基。缺乏蓝藻的嗜水杆菌(Plectonema boryanum)缺乏chIL的突变体无法在黑暗中合成叶绿素(Chl),从而导致Chl的合成像被子植物一样变得依赖光。当将突变细胞在黑暗中异养培养时,Chl合成被阻止,并且Chl含量以与细胞繁殖相反的方式呈指数下降,这表明大多数先前存在的Chl被募集为子细胞。在此“除泡”过程中,Chl含量小于原始含量的0.5%。与此平行的是,光系统I(PSI)的活性,其核心Chl结合亚基PsaA / PsaB和外围亚基PsaC的量降低。在停止Chl合成后,这些亚基的转录水平没有明显改变。相反,在D1和CP47的活性和蛋白质水平方面,光系统II(PSII)在显着程度上一直保持到黄化后期,这意味着尽管Chl合成被中止,PSII还是新合成的。低温(77 K)荧光光谱分析支持与PSI相关的Chl选择性降低。两者合计,建议可以释放和重新分布在PSI外围的原有Chl分子,以便在黄化蓝细菌细胞中进行PSII生物合成。 [参考:48]

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