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Deoxyribonucleic acid sequence of a gene from the Pseudomonas transposon TN501 encoding mercuric reductase

Brown, Nigel L., Ford, Simon J., Pridmore, R. David, Fritzinger, David C.·1983·Biochemistry

Abstract

We have determined the nucleotide sequence of the merA gene from the mercury-resistance transposon Tn501 and have predicted the structure of the gene product, mercuric reductase. The DNA sequence predicts a polypeptide of Mr 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 Pseudomonas 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.

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Metadata

Authors
Brown, N. L., Ford, S. J., Pridmore, R. D., & Fritzinger, D. C.
Venue
Biochemistry
Published
1983-08-16
Volume
22
Issue
17
Pages
4089-4095
ISSN
  • 0006-2960 (ISSN-L)
  • 1520-4995
OpenAlex
W2295412389
Cited by
225
References
0
FWCI
10.60
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Deoxyribonucleic acid sequence of a gene from the Pseudomonas transposon TN501 encoding mercuric reductase. https://app.cochat.ai/papers/10.1021/bi00286a015
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Brown, N. L., Ford, S. J., Pridmore, R. D., & Fritzinger, D. C. (1983). Deoxyribonucleic acid sequence of a gene from the Pseudomonas transposon TN501 encoding mercuric reductase. Biochemistry. https://doi.org/10.1021/bi00286a015

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