Literature DB >> 9224947

Cloning and analysis of the dnaG gene encoding Pseudomonas putida DNA primase.

P Szafranski1, C L Smith, C R Cantor.   

Abstract

The dnaG gene coding for primase, a key enzyme in DNA replication, has been isolated from chromosomal DNA of the soil bacterium Pseudomonas putida. It maps within the putative MMS operon, between the rpsU and rpoD genes. Comparison of the deduced amino acid sequence of P. putida DnaG with sequences of other known bacterial primases reveals the presence of a possible regulatory region which would be unique to pseudomonads. The analysis of nucleotide sequence suggests that stable folding of the dnaG mRNA may significantly contribute to the low level of its expression within a cell.

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Year:  1997        PMID: 9224947     DOI: 10.1016/s0167-4781(97)00059-6

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  3 in total

1.  Two distantly homologous DnaG primases from Thermoanaerobacter tengcongensis exhibit distinct initiation specificities and priming activities.

Authors:  Jie Li; Jingfang Liu; Ligang Zhou; Huadong Pei; Jian Zhou; Hua Xiang
Journal:  J Bacteriol       Date:  2010-03-26       Impact factor: 3.490

2.  A mutant Escherichia coli primase defective in elongation of primer RNA chains.

Authors:  W Sun; J Schoneich; G N Godson
Journal:  J Bacteriol       Date:  1999-06       Impact factor: 3.490

3.  Role of conserved amino acids in the catalytic activity of Escherichia coli primase.

Authors:  Anna Rodina; G Nigel Godson
Journal:  J Bacteriol       Date:  2006-05       Impact factor: 3.490

  3 in total

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