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光对荚膜红细菌中成熟B800 - 850捕光复合体稳态水平的转录后调控

Posttranscriptional regulation by light of the steady-state levels of mature B800-850 light-harvesting complexes in Rhodobacter capsulatus.

作者信息

Zucconi A P, Beatty J T

机构信息

Department of Microbiology, University of British Columbia, Vancouver, Canada.

出版信息

J Bacteriol. 1988 Feb;170(2):877-82. doi: 10.1128/jb.170.2.877-882.1988.

Abstract

Photosynthetic organisms exhibit a variety of responses to changes in light intensity, including differential biosynthesis of chlorophyll-protein complexes. Cultures of Rhodobacter capsulatus grown anaerobically with a low intensity of light (2 W/m2) contained about four times as much B800-850 light-harvesting complex as cells grown under high light intensity (140 W/m2). The mRNA transcripts encoding B800-850 beta and alpha peptides were analyzed by Northern blot (RNA blot), S1 nuclease protection, and capping with guanylyl transferase. It was found that the steady-state levels of B800-850 mRNAs in high-light-grown cultures were about four times as great as in cells grown under low light intensity. Therefore, the lesser amounts of mature B800-850 peptide gene products found in cells grown with high light intensity are the result of a posttranscriptional regulatory process. It was also found that there are two polycistronic messages encoding the B800-850 peptides. These messages share a common 3' terminus but differ in their 5'-end segments as a result of transcription initiation at two discrete sites. Moreover, the half-lives of B800-850 mRNAs were about 10 min in cells grown with high light and approximately 19 min in cultures grown with low light. It is concluded that there must be more frequent initiations of transcription of B800-850 genes in cells grown with high light than in those grown with low light, and that the relative amounts of B800-850 complexes under these conditions are controlled by a translational or posttranslational mechanism.

摘要

光合生物对光照强度的变化表现出多种反应,包括叶绿素 - 蛋白质复合物的差异生物合成。在低光照强度(2 W/m²)下厌氧培养的荚膜红细菌培养物中,B800 - 850光捕获复合物的含量约为在高光照强度(140 W/m²)下生长的细胞中的四倍。通过Northern印迹(RNA印迹)、S1核酸酶保护和用鸟苷酸转移酶加帽的方法分析了编码B800 - 850β和α肽的mRNA转录本。结果发现,在高光培养的细胞中,B800 - 850 mRNA的稳态水平约为低光培养细胞中的四倍。因此,在高光强度下生长的细胞中发现的成熟B800 - 850肽基因产物数量较少是转录后调控过程的结果。还发现有两个多顺反子信息编码B800 - 850肽。这些信息共享一个共同的3'末端,但由于在两个离散位点的转录起始,它们的5'末端片段不同。此外,B800 - 850 mRNA的半衰期在高光培养的细胞中约为10分钟,在低光培养的细胞中约为19分钟。可以得出结论,与低光培养的细胞相比,高光培养的细胞中B800 - 850基因的转录起始频率必须更高,并且在这些条件下B800 - 850复合物的相对含量受翻译或翻译后机制的控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f275/210736/1a1578d585cc/jbacter00180-0403-a.jpg

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