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蓝藻聚球藻属PCC 7002菌株recA基因的分子克隆与特性分析

Molecular cloning and characterization of the recA gene from the cyanobacterium Synechococcus sp. strain PCC 7002.

作者信息

Murphy R C, Bryant D A, Porter R D, de Marsac N T

出版信息

J Bacteriol. 1987 Jun;169(6):2739-47. doi: 10.1128/jb.169.6.2739-2747.1987.

Abstract

The recA gene of Synechococcus sp. strain PCC 7002 was detected and cloned from a lambda gtwes genomic library by heterologous hybridization by using a gene-internal fragment of the Escherichia coli recA gene as the probe. The gene encodes a 38-kilodalton polypeptide which is antigenically related to the RecA protein of E. coli. The nucleotide sequence of a portion of the gene was determined. The translation of this region was 55% homologous to the E. coli protein; allowances for conservative amino acid replacements yield a homology value of about 74%. The cyanobacterial recA gene product was proficient in restoring homologous recombination and partial resistance to UV irradiation to recA mutants of E. coli. Heterologous hybridization experiments, in which the Synechococcus sp. strain PCC 7002 recA gene was used as the probe, indicate that a homologous gene is probably present in all cyanobacterial strains.

摘要

通过使用大肠杆菌recA基因的基因内部片段作为探针,经异源杂交从λgtwes基因组文库中检测并克隆了聚球藻属PCC 7002菌株的recA基因。该基因编码一种38千道尔顿的多肽,其在抗原性上与大肠杆菌的RecA蛋白相关。测定了该基因部分区域的核苷酸序列。该区域的翻译产物与大肠杆菌蛋白有55%的同源性;考虑保守氨基酸替换后,同源性值约为74%。蓝藻recA基因产物能够有效恢复大肠杆菌recA突变体的同源重组能力和对紫外线照射的部分抗性。以聚球藻属PCC 7002菌株recA基因为探针的异源杂交实验表明,所有蓝藻菌株中可能都存在同源基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95e1/212179/5737426c77ca/jbacter00196-0429-a.jpg

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