首页> 外文期刊>Archives of microbiology >CLONING AND SEQUENCING OF THE GENES ENCODING THE LIGHT-HARVESTING B806-866 POLYPEPTIDES AND INITIAL STUDIES ON THE TRANSCRIPTIONAL ORGANIZATION OF PUF2B, PUF2A AND PUF2C IN CHLOROFLEXUS AURANTIACUS
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CLONING AND SEQUENCING OF THE GENES ENCODING THE LIGHT-HARVESTING B806-866 POLYPEPTIDES AND INITIAL STUDIES ON THE TRANSCRIPTIONAL ORGANIZATION OF PUF2B, PUF2A AND PUF2C IN CHLOROFLEXUS AURANTIACUS

机译:聚光捕获B806-866多肽的基因的克隆和序列分析及在桔梗中PUF2B,PUF2A和PUF2C的转录组织的初步研究

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The genes encoding the alpha- and beta-polypeptide subunits of the B806-866 membrane-bound light-harvesting complex of Chloroflexus aurantiacus have been cloned and the nucleotide sequences determined. The gene puf2A, which encodes the B806-866 alpha-polypeptide, began 28 bases downstream of the stop codon of puf2B, which encodes the B806-866 beta gene. The gene-encoding cytochrome c-554, puf2C, was found about 250 bp downstream of puf2A. puf2A encoded a 13 amino acid extension at the C-terminus of the B806-866 a-polypeptide that was not present in the mature protein. These genes, unlike those of purple nonsulfur bacteria, did not form a contiguous operon with puf1L or puf1M, the genes encoding the L and M subunits of the photochemical reaction center. The occurrence of the two latter genes and of puf2B and puf2A in two separate operons has not been observed in purple bacteria. Under photoheterotrophic growth conditions, puf2B and puf2A were encoded on an abundant mRNA that was 0.5 kb long. Two monocistronic transcripts for puf2C were observed that had different 5'-ends. One transcript encoding all three genes was also detected. Nucleotide sequences very similar to the consensus promoter sequence of the Escherichia coli RNA polymerase sigma(70) subunit were found seven and eight bases upstream of the 5'-end of mRNA encoding puf2B and for one of the monocistronic mRNA encoding puf2C, respectively. [References: 43]
机译:已经克隆了编码金绿藻弯曲杆菌B806-866膜结合的光捕获复合物的α-和β-多肽亚基的基因,并确定了核苷酸序列。编码B806-866α-多肽的基因puf2A在puf2B终止密码子下游28个碱基处开始,该密码子编码B806-866β基因。发现编码基因的细胞色素c-554 puf2C位于puf2A下游约250 bp。 puf2A在成熟蛋白中不存在的B806-866α-多肽的C端编码了13个氨基酸的延伸。这些基因与紫色非硫细菌的基因不同,它们不会与puf1L或puf1M形成连续的操纵子,而puf1L或puf1M是编码光化学反应中心L和M亚基的基因。在紫色细菌中尚未观察到后两个基因以及两个独立操纵子中的puf2B和puf2A的出现。在光异养生长条件下,puf2B和puf2A编码在0.5 kb长的丰富mRNA上。观察到puf2C的两个单顺反子转录物具有不同的5'-末端。还检测到一个编码所有三个基因的转录本。发现与大肠杆菌RNA聚合酶sigma(70)亚基的共有启动子序列非常相似的核苷酸序列被发现分别位于编码puf2B的mRNA的5'端上游7个和8个碱基和编码puf2C的单顺反子mRNA之一。 [参考:43]

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