Literature DB >> 3185509

Comparative analysis of genes encoding methyl coenzyme M reductase in methanogenic bacteria.

A Klein1, R Allmansberger, M Bokranz, S Knaub, B Müller, E Muth.   

Abstract

The sequence of the gene cluster encoding the methyl coenzyme M reductase (MCR) in Methanococcus voltae was determined. It contains five open reading frames (ORF), three of which encode the known enzyme subunits. Putative ribosome binding sites were found in front of all ORFs. They differ in their degrees of complementarity to the 3' end of the 16 S rRNA, which is discussed in terms of different translation efficiencies of the respective genes. The codon usage bias is different in the subunit encoding genes compared with the two other ORFs in the cluster and two other known genes of Mc. voltae. This is interpreted in terms of increased translational accuracy of the highly expressed MCR subunit genes. The derived polypeptide sequences encoded by the five ORFs of the MCR cluster were compared to those of the respective genes in Methanobacterium thermoautotrophicum Marburg and Methanosarcina barkeri. Conserved regions were detected in the enzyme subunits, which are candidates for factor binding domains. Conserved hydrophobic sequences found in the alpha and beta subunits are discussed with respect to the membrane association of the enzyme.

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Year:  1988        PMID: 3185509     DOI: 10.1007/bf00339610

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  35 in total

1.  Nucleotide sequence of the methyl coenzyme M reductase gene cluster from Methanosarcina barkeri.

Authors:  M Bokranz; A Klein
Journal:  Nucleic Acids Res       Date:  1987-05-26       Impact factor: 16.971

2.  Structure and methylation of coenzyme M(HSCH2CH2SO3).

Authors:  C D Taylor; R S Wolfe
Journal:  J Biol Chem       Date:  1974-08-10       Impact factor: 5.157

Review 3.  Methanogens: reevaluation of a unique biological group.

Authors:  W E Balch; G E Fox; L J Magrum; C R Woese; R S Wolfe
Journal:  Microbiol Rev       Date:  1979-06

4.  Adjustment of the tRNA population to the codon usage in chloroplasts.

Authors:  H Pfitzinger; P Guillemaut; J H Weil; D T Pillay
Journal:  Nucleic Acids Res       Date:  1987-02-25       Impact factor: 16.971

5.  The pIC plasmid and phage vectors with versatile cloning sites for recombinant selection by insertional inactivation.

Authors:  J L Marsh; M Erfle; E J Wykes
Journal:  Gene       Date:  1984-12       Impact factor: 3.688

6.  Novel bacteriophage lambda cloning vector.

Authors:  J Karn; S Brenner; L Barnett; G Cesareni
Journal:  Proc Natl Acad Sci U S A       Date:  1980-09       Impact factor: 11.205

7.  Lambda replacement vectors carrying polylinker sequences.

Authors:  A M Frischauf; H Lehrach; A Poustka; N Murray
Journal:  J Mol Biol       Date:  1983-11-15       Impact factor: 5.469

8.  A simple method for displaying the hydropathic character of a protein.

Authors:  J Kyte; R F Doolittle
Journal:  J Mol Biol       Date:  1982-05-05       Impact factor: 5.469

9.  Doublet frequencies in evolutionary distinct groups.

Authors:  R Nussinov
Journal:  Nucleic Acids Res       Date:  1984-02-10       Impact factor: 16.971

10.  Structure and expression of the genes, mcrBDCGA, which encode the subunits of component C of methyl coenzyme M reductase in Methanococcus vannielii.

Authors:  D S Cram; B A Sherf; R T Libby; R J Mattaliano; K L Ramachandran; J N Reeve
Journal:  Proc Natl Acad Sci U S A       Date:  1987-06       Impact factor: 11.205

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  16 in total

1.  Purification and properties of methyl coenzyme M methylreductase from acetate-grown Methanosarcina thermophila.

Authors:  P E Jablonski; J G Ferry
Journal:  J Bacteriol       Date:  1991-04       Impact factor: 3.490

2.  Methanococcus voltae harbors four gene clusters potentially encoding two [NiFe] and two [NiFeSe] hydrogenases, each of the cofactor F420-reducing or F420-non-reducing types.

Authors:  S Halboth; A Klein
Journal:  Mol Gen Genet       Date:  1992-05

3.  Identification of the mcrD gene product and its association with component C of methyl coenzyme M reductase in Methanococcus vannielii.

Authors:  B A Sherf; J N Reeve
Journal:  J Bacteriol       Date:  1990-04       Impact factor: 3.490

Review 4.  Methanogenesis: genes, genomes, and who's on first?

Authors:  J N Reeve; J Nölling; R M Morgan; D R Smith
Journal:  J Bacteriol       Date:  1997-10       Impact factor: 3.490

5.  Construction of an integration vector for use in the archaebacterium Methanococcus voltae and expression of a eubacterial resistance gene.

Authors:  P Gernhardt; O Possot; M Foglino; L Sibold; A Klein
Journal:  Mol Gen Genet       Date:  1990-04

6.  Isolation and identification of methanogen-specific DNA from blanket bog peat by PCR amplification and sequence analysis.

Authors:  B A Hales; C Edwards; D A Ritchie; G Hall; R W Pickup; J R Saunders
Journal:  Appl Environ Microbiol       Date:  1996-02       Impact factor: 4.792

7.  Insertional Mutations in the Hydrogenase vhc and frc Operons Encoding Selenium-Free Hydrogenases in Methanococcus voltae.

Authors:  Y Berghofer; A Klein
Journal:  Appl Environ Microbiol       Date:  1995-05       Impact factor: 4.792

8.  Characterization and phylogeny of mcrII, a gene cluster encoding an isoenzyme of methyl coenzyme M reductase from hyperthermophilic Methanothermus fervidus.

Authors:  A Lehmacher; H P Klenk
Journal:  Mol Gen Genet       Date:  1994-04

9.  Cloning, sequencing, and growth phase-dependent transcription of the coenzyme F420-dependent N5,N10-methylenetetrahydromethanopterin reductase-encoding genes from Methanobacterium thermoautotrophicum delta H and Methanopyrus kandleri.

Authors:  J Nölling; T D Pihl; J N Reeve
Journal:  J Bacteriol       Date:  1995-12       Impact factor: 3.490

10.  Methyl-coenzyme M reductase and other enzymes involved in methanogenesis from CO2 and H2 in the extreme thermophile Methanopyrus kandleri.

Authors:  S Rospert; J Breitung; K Ma; B Schwörer; C Zirngibl; R K Thauer; D Linder; R Huber; K O Stetter
Journal:  Arch Microbiol       Date:  1991       Impact factor: 2.552

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