Literature DB >> 2045372

Protein synthesis in vitro by Micrococcus luteus.

M A Farwell1, J C Rabinowitz.   

Abstract

Bacillus subtilis and related gram-positive bacteria which have low to moderate genomic G + C contents are unable to efficiently translate mRNA derived from gram-negative bacteria, whereas Escherichia coli and other gram-negative bacteria are able to translate mRNA from both types of organisms. This phenomenon has been termed translational species specificity. Ribosomes from the low-G + C-content group (low-G + C group) of gram-positive organisms (B. subtilis and relatives) lack an equivalent to Escherichia ribosomal protein S1. The requirement for S1 for translation in E. coli (G. van Dieijen, P. H. van Knippenberg, J. van Duin, B. Koekman, and P. H. Pouwels, Mol. Gen. Genet. 153:75-80, 1977) and its specific role (A.R. Subramanian, Trends Biochem. Sci. 9:491-494, 1984) have been proposed. The group of gram-positive bacteria characterized by high genomic G + C content (formerly Actinomyces species and relatives) contain S1, in contrast to the low-G + C group (K. Mikulik, J. Smardova, A. Jiranova, and P. Branny, Eur. J. Biochem. 155:557-563, 1986). It is not known whether members of the high-G + C group are translationally specific, although there is evidence that one genus, Streptomyces, can express Escherichia genes in vivo (M. J. Bibb and S. N. Cohen, Mol. Gen. Genet. 187:265-277, 1985; J. L. Schottel, M. J. Bibb, and S. N. Cohen, J. Bacteriol. 146:360-368, 1981). In order to determine whether the organisms of this group are translationally specific, we examined the in vitro translational characteristics of a member of the high-G + C group, Micrococcus luteus, whose genomic G + C content is 73%. A semipurified coupled transcription-translation system of M. luteus translates Escherichia mRNA as well as Bacillus and Micrococcus mRNA. Therefore, M. luteus is translationally nonspecific and resembles E. coli rather than B. subtilis in its translational characteristics.

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Year:  1991        PMID: 2045372      PMCID: PMC207966          DOI: 10.1128/jb.173.11.3514-3522.1991

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  31 in total

1.  Quantitative film detection of 3H and 14C in polyacrylamide gels by fluorography.

Authors:  R A Laskey; A D Mills
Journal:  Eur J Biochem       Date:  1975-08-15

2.  The effect of the ribosomal protein S1 from Escherichia coli on the synthesis in vitro of bacterial-, DNA phage- and RNA phage proteins.

Authors:  G van Dieijen; P H van Knippenberg; J van Duin; B Koekman; P H Pouwels
Journal:  Mol Gen Genet       Date:  1977-05-20

3.  Initiation of protein synthesis in vitro by a clostridial system. I. Specificity in the translation of natural messenger ribonucleic acids.

Authors:  M R Stallcup; J C Rabinowitz
Journal:  J Biol Chem       Date:  1973-05-10       Impact factor: 5.157

4.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

5.  Specificity of bacterial ribosomes and messenger ribonucleic acids in protein synthesis reactions in vitro.

Authors:  M R Stallcup; W J Sharrock; J C Rabinowitz
Journal:  J Biol Chem       Date:  1976-04-25       Impact factor: 5.157

6.  Comparison of procedures for extracting transfer RNA from spores of Bacillus.

Authors:  B Vold; S Minatogawa
Journal:  Arch Biochem Biophys       Date:  1972-03       Impact factor: 4.013

7.  Spectinomycin operon of Micrococcus luteus: evolutionary implications of organization and novel codon usage.

Authors:  T Ohama; A Muto; S Osawa
Journal:  J Mol Evol       Date:  1989-11       Impact factor: 2.395

8.  Cell-free synthesis of proteins coding for mobilisation functions of ColE1 and transposition functions of Tn3.

Authors:  J Collins
Journal:  Gene       Date:  1979-05       Impact factor: 3.688

9.  Translation of synthetic and endogenous messenger ribonucleic acid in vitro by ribosomes and polyribosomes from Clostridium pasteurianum.

Authors:  R H Himes; M R Stallcup; J C Rabinowitz
Journal:  J Bacteriol       Date:  1972-12       Impact factor: 3.490

10.  Natural messenger ribonucleic acid-directed cell-free protein-synthesizing system of Bacillus subtilis.

Authors:  L Legault-Demare; G H Chambliss
Journal:  J Bacteriol       Date:  1974-12       Impact factor: 3.490

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  2 in total

1.  Exploiting unassigned codons in Micrococcus luteus for tRNA-based amino acid mutagenesis.

Authors:  A K Kowal; J S Oliver
Journal:  Nucleic Acids Res       Date:  1997-11-15       Impact factor: 16.971

2.  Probing the relationship between Gram-negative and Gram-positive S1 proteins by sequence analysis.

Authors:  Philippe Salah; Marco Bisaglia; Pascale Aliprandi; Marc Uzan; Christina Sizun; François Bontems
Journal:  Nucleic Acids Res       Date:  2009-07-15       Impact factor: 16.971

  2 in total

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