Literature DB >> 3326786

Determination of the nucleotide sequence for the glutamate synthase structural genes of Escherichia coli K-12.

G Oliver1, G Gosset, R Sanchez-Pescador, E Lozoya, L M Ku, N Flores, B Becerril, F Valle, F Bolivar.   

Abstract

We have determined the complete nucleotide sequence of a 6.3-kb chromosomal HpaI-EcoRI fragment, that contains the structural genes for both the large and small subunits of the Escherichia coli K-12 glutamate synthase (GOGAT) enzyme, as well as the 5'- and 3'-flanking and intercistronic DNA regions. The Mrs of the two subunits, as deduced from the nucleotide (nt) sequence, were estimated as 166,208 and 52,246. Partial amino acid sequence of the GOGAT enzyme revealed that the large subunit starts with a cysteine residue that is probably generated by a proteolytic cleavage. Northern blotting experiments revealed a transcript of approximately 7300 nt, that at least contains the cistrons for both subunits. A transcriptional start point and a functional promoter were identified in the 5' DNA flanking region of the large subunit gene. The messenger RNA nontranslated leader region has 120 nt and shares identity with the leader regions of E. coli ribosomal operons, in particular around the so-called boxA sequence implicated in antitermination. Other possible regulatory sequences are described.

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Year:  1987        PMID: 3326786     DOI: 10.1016/0378-1119(87)90207-1

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  31 in total

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5.  Mutations affecting the Shine-Dalgarno sequences of the untranslated region of the Escherichia coli gltBDF operon.

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6.  Purification and properties of tobacco ferredoxin-dependent glutamate synthase, and isolation of corresponding cDNA clones : Light-inducibility and organ-specificity of gene transcription and protein expression.

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Review 8.  Linkage map of Escherichia coli K-12, edition 10: the traditional map.

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9.  Amino-terminal deletions define a glutamine amide transfer domain in glutamine phosphoribosylpyrophosphate amidotransferase and other PurF-type amidotransferases.

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