首页> 外文期刊>Biochimica et biophysica acta. Bioenergetics >The 9-kDa phosphoprotein of photosystem II. Generation and characterisation of Chlamydomonas mutants lacking PSII-H and a site-directed mutant lacking the phosphorylation site
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The 9-kDa phosphoprotein of photosystem II. Generation and characterisation of Chlamydomonas mutants lacking PSII-H and a site-directed mutant lacking the phosphorylation site

机译:光系统II的9 kDa磷蛋白。缺乏PSII-H的衣原体突变体和缺少磷酸化位点的定点突变体的产生和表征

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摘要

The chloroplast gene psbH encodes a 9-10 kDa thylakoid membrane protein (PSII-H) that is associated with photosystem II and is subject to light-dependent phosphorylation at a threonine residue located on the stromal side of the membrane. The function of PSII-H is not known, neither is it clear what regulatory role phosphorylation may play in the control of PSII activity. Using particle gun-mediated transformation, we have created chloroplast transformants of Chlamydomonas reinhardtii in which the synthesis of PSII-H is prevented by the disruption of psbH, or in which the phosphorylatable threonine is replaced by alanine through site-directed mutagenesis of the gene. The mutants lacking PSII-H have a photosystem II-deficient phenotype, with no detectable functioning PSII complex present in whole cells or isolated thylakoid membranes. In contrast, the alanine mutant (T3A) grows photoautotrophically, and PSII activity is comparable to wild-type cells as determined by various biochemical and biophysical assays.
机译:叶绿体基因psbH编码与光系统II相关的9-10 kDa类囊体膜蛋白(PSII-H),并在位于膜基质侧的苏氨酸残基处受到光依赖的磷酸化作用。 PSII-H的功能尚不清楚,也不清楚磷酸化在PSII活性控制中可能起什么调节作用。使用粒子枪介导的转化,我们创建了莱茵衣藻的叶绿体转化体,其中通过psbH的破坏阻止了PSII-H的合成,或者通过基因的定点诱变将可磷酸化的苏氨酸替换成了丙氨酸。缺少PSII-H的突变体具有光系统II缺陷型,在整个细胞或分离的类囊体膜中均没有可检测到的功能性PSII复合物。相比之下,丙氨酸突变体(T3A)光合自养,通过各种生化和生物物理分析确定,PSII活性与野生型细胞相当。

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