Literature DB >> 3997817

Nucleotide sequence of the luxA gene of Vibrio harveyi and the complete amino acid sequence of the alpha subunit of bacterial luciferase.

D H Cohn, A J Mileham, M I Simon, K H Nealson, S K Rausch, D Bonam, T O Baldwin.   

Abstract

The nucleotide sequence of the 1.85-kilobase EcoRI fragment from Vibrio harveyi that was cloned using a mixed-sequence synthetic oligonucleotide probe (Cohn, D. H., Ogden, R. C., Abelson, J. N., Baldwin, T. O., Nealson, K. H., Simon, M. I., and Mileham, A. J. (1983) Proc. Natl. Acad. Sci. U.S.A. 80, 120-123) has been determined. The alpha subunit-coding region (luxA) was found to begin at base number 707 and end at base number 1771. The alpha subunit has a calculated molecular weight of 40,108 and comprises a total of 355 amino acid residues. There are 34 base pairs separating the start of the alpha subunit structural gene and a 669-base open reading frame extending from the proximal EcoRI site. At the 3' end of the luxA coding region there are 26 bases between the end of the structural gene and the start of the luxB structural gene. Approximately two-thirds of the alpha subunit was sequenced by protein chemical techniques. The amino acid sequence implied by the DNA sequence, with few exceptions, confirmed the chemically determined sequence. Regions of the alpha subunit thought to comprise the active center were found to reside in two discrete and relatively basic regions, one from around residues 100-115 and the second from around residues 280-295.

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Year:  1985        PMID: 3997817

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  32 in total

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Journal:  Microbiol Rev       Date:  1991-03

2.  Analysis of the bacterial luciferase mobile loop by replica-exchange molecular dynamics.

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4.  Expression and assembly of functional bacterial luciferase in plants.

Authors:  C Koncz; O Olsson; W H Langridge; J Schell; A A Szalay
Journal:  Proc Natl Acad Sci U S A       Date:  1987-01       Impact factor: 11.205

5.  Use of controlled luciferase expression to monitor chemicals affecting protein synthesis.

Authors:  J Lampinen; M Virta; M Karp
Journal:  Appl Environ Microbiol       Date:  1995-08       Impact factor: 4.792

6.  Development of species-specific hybridization probes for marine luminous bacteria by using in vitro DNA amplification.

Authors:  C F Wimpee; T L Nadeau; K H Nealson
Journal:  Appl Environ Microbiol       Date:  1991-05       Impact factor: 4.792

7.  Bacterial luciferase as a reporter of circadian gene expression in cyanobacteria.

Authors:  Y Liu; S S Golden; T Kondo; M Ishiura; C H Johnson
Journal:  J Bacteriol       Date:  1995-04       Impact factor: 3.490

8.  cis-acting sequences required for NtcB-dependent, nitrite-responsive positive regulation of the nitrate assimilation operon in the cyanobacterium Synechococcus sp. strain PCC 7942.

Authors:  S Maeda; Y Kawaguchi; T A Ohe; T Omata
Journal:  J Bacteriol       Date:  1998-08       Impact factor: 3.490

9.  The use of the luxA gene of the bacterial luciferase operon as a reporter gene.

Authors:  O Olsson; C Koncz; A A Szalay
Journal:  Mol Gen Genet       Date:  1988-12

10.  Expression of bioluminescence by Escherichia coli containing recombinant Vibrio harveyi DNA.

Authors:  C Miyamoto; D Byers; A F Graham; E A Meighen
Journal:  J Bacteriol       Date:  1987-01       Impact factor: 3.490

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