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Cloning of the Escherichia coli recJ chromosomal region and identification of its encoded proteins.

A 9.6-kilobase BamHI-SalI fragment carrying recJ+ was cloned into vector pBR322. Deletion and transposon mutagenesis were used to map the recJ gene on this fragment. The maxicell protein-labeling technique was used to correlate a functional recJ gene with the presence of a polypeptide of 53,000 appa...

詳細記述

保存先:
書誌詳細
主要な著者: Lovett, S T, Clark, A J
フォーマット: Artigo
言語:Inglês
出版事項: 1985
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC218986/
https://ncbi.nlm.nih.gov/pubmed/2984175
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