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聚球藻属PCC 6701菌株和组装突变体UV16中藻蓝蛋白亚基的基因。

Genes for phycocyanin subunits in Synechocystis sp. strain PCC 6701 and assembly mutant UV16.

作者信息

Anderson L K, Grossman A R

机构信息

Department of Plant Biology, Carnegie Institution of Washington, Stanford, California 94305.

出版信息

J Bacteriol. 1990 Mar;172(3):1289-96. doi: 10.1128/jb.172.3.1289-1296.1990.

Abstract

The cyanobacterial phycobilisome is a large protein complex located on the photosynthetic membrane. It harvests light energy and transfers it to chlorophyll for use in photosynthesis. Phycobilisome assembly mutants in the unicellular cyanobacterium Synechocystis sp. strain 6701 have been characterized. One such mutant, UV16, contains a defect in the assembly of the biliprotein phycocyanin. We report the cloning and sequencing of the phycocyanin genes from wild-type Synechocystis strain 6701 and demonstrate an alteration in the gene for the phycocyanin alpha subunit in UV16. Possible consequences of the lesion on phycobilisome assembly were assessed from its position in the phycocyanin tertiary and quaternary structures. The UV16 phenotype is complex and includes a reduced level of phycocyanin relative to that in the wild type. To determine whether the lower phycocyanin content results from lower transcript levels, a fragment of cpcBA was used as a probe for quantitating phycocyanin mRNA. Both the wild type and UV16 contained two phycocyanin transcripts of approximately 1.4 and 1.5 kilobases that were equal in abundance and that did not vary with light quality during cell growth. Equal levels of these transcripts in the wild type and UV16 suggest that the lower phycocyanin content in the mutant may be due to posttranscriptional events. The 5' ends of the two phycocyanin mRNAs were mapped at 100 and 223 base pairs upstream of the cpcB initiation codon. Homologous regions upstream of the putative transcription initiation sites may be important for maintaining high levels of transcription from the Synechocystis strain 6701 phycocyanin gene set.

摘要

蓝藻藻胆体是一种位于光合膜上的大型蛋白质复合体。它收集光能并将其传递给叶绿素以供光合作用使用。单细胞蓝藻集胞藻6803中的藻胆体组装突变体已得到鉴定。其中一个这样的突变体UV16,在双蛋白藻蓝蛋白的组装中存在缺陷。我们报道了野生型集胞藻6803藻蓝蛋白基因的克隆和测序,并证明UV16中藻蓝蛋白α亚基的基因发生了改变。从其在藻蓝蛋白三级和四级结构中的位置评估了该损伤对藻胆体组装的可能影响。UV16的表型很复杂,相对于野生型,其藻蓝蛋白水平降低。为了确定较低的藻蓝蛋白含量是否是由于转录水平较低导致的,使用cpcBA片段作为探针来定量藻蓝蛋白mRNA。野生型和UV16都含有两条约1.4和1.5千碱基的藻蓝蛋白转录本,它们的丰度相等,并且在细胞生长过程中不随光质变化。野生型和UV16中这些转录本水平相等,表明突变体中较低的藻蓝蛋白含量可能是由于转录后事件导致的。两条藻蓝蛋白mRNA的5'端位于cpcB起始密码子上游100和223个碱基对处。假定转录起始位点上游的同源区域对于维持集胞藻6803藻蓝蛋白基因组高水平转录可能很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff5/208597/4fabe355acdc/jbacter01045-0138-a.jpg

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