Home LiteratureArticle Details
PMID: 6754698 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Characterization of Escherichia coli men mutants defective in conversion of o-succinylbenzoate to 1,4-dihydroxy-2-naphthoate.

Journal of bacteriology ·Vol. 152 ·No. 3 ·1982-12-00 ·Pages 1132-7

Shaw DJ, Guest JR, Meganathan R, Bentley R

Abstract

Four independent menaquinone (vitamin K(2))-deficient mutants of Escherichia coli, blocked in the conversion of o-succinylbenzoate (OSB) to 1,4-dihydroxy-2-naphthoate (DHNA), were found to represent two distinct classes. Enzymatic complementation was observed when a cell-free extract of one mutant was mixed with extracts of any of the remaining three mutants. The missing enzymes in the two classes were identified by in vitro complementation with preparations of OSB-coenzyme A (CoA) synthetase or DHNA synthase isolated from Mycobacterium phlei. Mutants lacking DHNA synthase (and therefore complementing with M. phlei DHNA synthase) were designated menB, and the mutant lacking OSB-CoA synthetase (and therefore complementing with M. phlei OSB-CoA synthetase) was designated menE. The menB mutants produced only the spirodilactone form of OSB when extracts were incubated with [2,3-(14)C(2)]OSB, ATP, and CoA; the OSB was unchanged on incubation with an extract from the menE mutant under these conditions. Experiments with strains lysogenized by a lambda men transducing phage (lambdaG68) and transduction studies with phage P1 indicated that the menB and menE genes form part of a cluster of four genes, controlling the early steps in menaquinone biosynthesis, located at 48.5 min in the E. coli linkage map. Evidence was obtained for the clockwise gene order gyrA....menC- 0000100000 0000110000 0011111000 0000111000 0011111000 0001110000 0000110101 0001111111 0001100000 0000100000 0001101100 0011111000 0011000000 0011000000 0111000111 0111101110 -B-D, where the asterisk denotes the uncertain position of menE relative to menC and menB. The transducing phage (lambdaG68) contained functional menB, menC, and menE genes, but only part of the menD gene, and it was designated lambda menCB(D).

MeSH Terms
Chromosome Mapping Chromosomes, Bacterial Coenzyme A Ligases/genetics Escherichia coli/genetics,metabolism Genes, Bacterial Hydro-Lyases/genetics Lysogeny Mutation Naphthols/metabolism Phenylbutyrates/metabolism Succinate-CoA Ligases/genetics Transduction, Genetic
Chemicals
Naphthols Phenylbutyrates 1,4-dihydroxy-2-naphthoic acid o-succinylbenzoic acid Hydro-Lyases naphthoate synthetase Coenzyme A Ligases Succinate-CoA Ligases O-succinylbenzoate - CoA ligase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Shaw D J
Guest J R
Meganathan R
Bentley R
References (18)
18 references, click to expand
  1. DNA targets for the Escherichia coli K restriction system analysed genetically in recombinants between phages phi80 and lambda.
    Mol Gen Genet. 1973 Feb 2;120(3):261-81 PMID: 4568839
  2. Biosynthesis of bacterial menaquinones. Menaquinone mutants of Escherichia coli.
    Biochemistry. 1975 Jan 28;14(2):399-406 PMID: 1091286
  3. Biosynthesis of bacterial menaquinones: the membrane-associated 1,4-dihydroxy-2-naphthoate octaprenyltransferase of Escherichia coli.
    Biochemistry. 1976 Jun 29;15(13):2754-8 PMID: 949474
  4. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.
    Anal Biochem. 1976 May 7;72:248-54 PMID: 942051
  5. Menaquinone biosynthesis: conversion of o-succinylbenzoic acid to 1,4-dihydroxy-2-naphthoic acid and menaquinones by Escherichia coli extracts.
    Biochemistry. 1976 Nov 2;15(22):4792-6 PMID: 791360
  6. Mutants of Escherichia coli K12 unable to use fumarate as an anaerobic electron acceptor.
    J Gen Microbiol. 1976 Dec;97(2):145-60 PMID: 796407
  7. Menaquinone biosynthesis: mutants of Escherichia coli K-12 requiring 2-succinylbenzoate.
    J Bacteriol. 1977 Jun;130(3):1038-46 PMID: 324971
  8. Isolation and properties of naphthoate synthetase from Mycobacterium phlei.
    Arch Biochem Biophys. 1978 May;188(1):56-63 PMID: 677895
  9. Menaquinone (vitamin K2) biosynthesis: conversion of o-succinylbenzoic acid to 1,4-dihydroxy-2-naphthoic acid by Mycobacterium phlei enzymes.
    J Bacteriol. 1979 Oct;140(1):92-8 PMID: 500558
  10. Anaerobic growth of Escherichia coli K12 with fumarate as terminal electron acceptor. Genetic studies with menaquinone and fluoroacetate-resistant mutants.
    J Gen Microbiol. 1979 Dec;115(2):259-71 PMID: 393800
  11. Conversion of o-succinylbenzoate to dihydroxynaphthoate by extracts of Micrococcus luteus.
    Biochemistry. 1980 Feb 19;19(4):785-9 PMID: 7356957
  12. Linkage map of Escherichia coli K-12, edition 6.
    Microbiol Rev. 1980 Mar;44(1):1-56 PMID: 6997720
  13. Menaquinone biosynthesis in Bacillus subtilis: isolation of men mutants and evidence for clustering of men genes.
    J Bacteriol. 1981 Jan;145(1):321-7 PMID: 6780514
  14. Identification of Bacillus subtilis men mutants which lack O-succinylbenzoyl-coenzyme A synthetase and dihydroxynaphthoate synthase.
    J Bacteriol. 1981 Jan;145(1):328-32 PMID: 6780515
  15. Molecular cloning of menaquinone biosynthetic genes of Escherichia coli K12.
    Mol Gen Genet. 1981;181(3):379-83 PMID: 6454056
  16. Enzymatic synthesis of the coenzyme A ester of o-succinylbenzoic acid, an intermediate in menaquinone (vitamin K2) biosynthesis.
    FEBS Lett. 1981 Jun 15;128(2):201-4 PMID: 7262311
  17. Biosynthesis of o-succinylbenzoic acid in a men- Escherichia coli mutant requires decarboxylation of L-glutamate at the C-1 position.
    Biochemistry. 1981 Sep 1;20(18):5336-40 PMID: 6117313
  18. ACTIVE TRANSPORT OF L-ALPHA-GLYCEROPHOSPHATE IN ESCHERICHIA COLI.
    J Biol Chem. 1964 Sep;239:3098-105 PMID: 14217902
Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1982-12-00
Pages
1132-7
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC221619
Subset
IM
Grants
NIGMS NIH HHS · GM 20053 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com