Deoxyribonucleic acid sequence of a gene from the Pseudomonas transposon TN501 encoding mercuric reductase
- 16 August 1983
- journal article
- research article
- Published by American Chemical Society (ACS) in Biochemistry
- Vol. 22 (17) , 4089-4095
- https://doi.org/10.1021/bi00286a015
Abstract
The nucleotide sequence of the merA gene from the Hg-resistance transposon Tn501 and have the structure of the gene product, mercuric reductase, was predicted. The DNA sequence predicts a polypeptide of MW 58,660, the primary structure of which shows strong homologies to glutathione reductase and lipoamide dehydrogenase, but mercuric reductase contains as additional N-terminal region that may form a separate domain. The implications of these comparisons for the tertiary structure and mechanism of mercuric reductase are discussed. The DNA sequence presented here has an overall G + C content of 65.1 mol%, typical of the bulk DNA of P. aeruginosa from which Tn501 was originally isolated. Analysis of the codon usage in the merA gene shows that codons with C or G at the third position are preferentially utilized.This publication has 2 references indexed in Scilit:
- Polypeptides encoded by the mer operonJournal of Bacteriology, 1982
- The tetracycline resistance transposons Tn1721 and Tn1771 have three 38-base-pair repeats and generate five-base-pair direct repeatsMolecular Genetics and Genomics, 1981