Literature DB >> 5357016

Inhibitory effects of pH5 enzyme from non-lactating bovine mammary gland on various stages of protein synthesis in the rat liver amino acid-incorporating system.

M D Herrington, A O Hawtrey.   

Abstract

1. pH5 enzyme from non-lactating bovine mammary gland was found to contain potent inhibitors of protein synthesis in the rat liver cell-free system. These inhibitors affect (a) formation of aminoacyl-tRNA where tRNA represents transfer RNA, (b) transfer of labelled amino acids from rat liver amino[(14)C]acyl-tRNA to protein in rat liver polyribosomes, and (c) incorporation of (14)C-labelled amino acids into peptide by rat liver polyribosomes supplemented with rat liver pH5 enzyme. 2. Increasing amounts of pH5 enzyme from bovine mammary gland progressively inhibited the incorporation of labelled amino acids into protein by a complete incorporating system from rat liver. Approx. 80% inhibition was observed at a concentration of 2mg. of protein of pH5 enzyme from bovine mammary gland. The inhibitory effect of the bovine pH5 enzyme fraction could not be overcome by the addition of increasing amounts of rat liver pH5 enzyme. 3. Fractionation of bovine pH5 enzyme with ammonium sulphate into four fractions showed that all the fractions inhibited the incorporation of (14)C-labelled amino acids in the rat liver system, but to varying extents. The highest inhibition observed (90%) was exhibited by the 60%-saturated-ammonium sulphate fraction. 4. Heat treatment of bovine pH5 enzyme at various temperatures caused only a partial loss of its inhibitory effect on labelled amino acid incorporation by the rat liver system. Treatment at 105 degrees for 5min. resulted in the bovine pH5 enzyme fraction losing 30% of its inhibitory activity. 5. pH5 enzyme from bovine mammary gland strongly inhibited the charging of rat liver tRNA in the presence of its own pH5 enzymes. 6. The transfer of labelled amino acids from rat liver amino[(14)C]acyl-tRNA to protein in a system containing rat liver polyribosomes and pH5 enzyme was almost completely inhibited by bovine pH5 enzyme at a concentration of 2mg. of protein of the enzyme fraction. 7. One of the inhibitors of various stages of protein synthesis in rat liver present in bovine pH5 enzyme was identified as an active ribonuclease, and the second inhibitor present was shown to be tRNA.

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Year:  1969        PMID: 5357016      PMCID: PMC1185192          DOI: 10.1042/bj1150671

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  18 in total

1.  ON THE STABILITY OF AMINOACYL-S-RNA TO NUCLEOPHILIC CATALYSIS.

Authors:  P S SARIN; P C ZAMECNIK
Journal:  Biochim Biophys Acta       Date:  1964-12-16

2.  Ribosomal aggregate engaged in protein synthesis: characterization of the ergosome.

Authors:  F O WETTSTEIN; T STAEHELIN; H NOLL
Journal:  Nature       Date:  1963-02-02       Impact factor: 49.962

3.  Lipo-amino acid complexes from Bacillus megaterium and their possible role in protein synthesis.

Authors:  G D HUNTER; R A GOODSALL
Journal:  Biochem J       Date:  1961-03       Impact factor: 3.857

4.  Passage of radioactive amino acids through nonprotein fractions of hen oviduct during incorporation into protein.

Authors:  R W HENDLER
Journal:  J Biol Chem       Date:  1959-06       Impact factor: 5.157

5.  The effect of guanosine diphosphate and triphosphate on the incorporation of labeled amino acids into proteins.

Authors:  E B KELLER; P C ZAMECNIK
Journal:  J Biol Chem       Date:  1956-07       Impact factor: 5.157

6.  Studies on azo-dye carcinogenesis in rat liver. The effect of 4-dimethylamino-3'-methylazobenzene on the incorporation of [C]leucine into rat-liver microsomal protein.

Authors:  A O Hawtrey; V Schirren; J Dijkstra
Journal:  Biochem J       Date:  1963-07       Impact factor: 3.857

7.  Studies on subcellular fractions of non-lactating bovine mamm- ary gland.

Authors:  M D Herrington; A O Hawtrey
Journal:  S Afr J Med Sci       Date:  1969-07

8.  The mechanism of protein synthesis in the developing chick embryo. The incorporation of free amino acids.

Authors:  N H Carey
Journal:  Biochem J       Date:  1964-05       Impact factor: 3.857

9.  Nuclease activity in cell-free amino acid-incorporating systems from chicken liver.

Authors:  J G Siler; M Fried
Journal:  Biochem J       Date:  1968-09       Impact factor: 3.857

10.  Inhibition by soluble ribonucleic acid of stimulatory effect of liver template ribonucleic acid.

Authors:  S A Aaronson; A Korner; A J Munro
Journal:  Biochem J       Date:  1966-11       Impact factor: 3.857

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  6 in total

1.  Differences in the ribosomes prepared from lactating and non-lactating bovine mammary gland.

Authors:  M D Herrington; A O Hawtrey
Journal:  Biochem J       Date:  1971-01       Impact factor: 3.857

2.  Cell-free protein synthesis in heart and skeletal muscles from polymyopathic hamsters.

Authors:  A J Bester; W Gevers
Journal:  Biochem J       Date:  1973-02       Impact factor: 3.857

3.  Evidence for defective transfer ribonucleic acid in polymyopathic hamsters and its inhibitory effect on protein synthesis.

Authors:  A J Bester; W Gevers
Journal:  Biochem J       Date:  1973-02       Impact factor: 3.857

4.  Evidence for the absence of the terminal adenine nucleotide at the amino acid-acceptor end of transfer ribonucleic acid in non-lactating bovine mammary gland and its inhibitory effect on the aminoacylation of rat liver transfer ribonucleic acid.

Authors:  M D Herrington; A O Hawtrey
Journal:  Biochem J       Date:  1970-02       Impact factor: 3.857

5.  Competing addition and hydrolysis of the cytidylylcytidylyladenosine terminal residues of transfer ribonucleic acid isolated from the non-lactating bovine mammary gland.

Authors:  M D Herrington; A O Hawtrey
Journal:  Biochem J       Date:  1970-09       Impact factor: 3.857

6.  Studies on the binding and distribution of radioactively labelled 3'-methylcholanthrene in subcellular fractions of rat liver.

Authors:  P A Jones; A O Hawtrey
Journal:  Br J Cancer       Date:  1971-12       Impact factor: 7.640

  6 in total

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