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PMID: 4317102 Published · ppublish English Journal Article

Comparison of lysyl-transfer ribonucleic acid species from vegetative cells and spores of Bacillus subtilis by methylated albumin-kieselguhr and reversed-phase chromatography.

Journal of bacteriology ·Vol. 102 ·No. 3 ·1970-06-00 ·Pages 711-5

Vold BS

Abstract

Lysyl-transfer ribonucleic acid (tRNA) species from a spore-forming strain of Bacillus subtilis (168 trp2(-)) and an early blocked asporogenous mutant (spoA 12) were compared on reversed-phase and methylated albumin-kieselguhr columns. Lysyl-tRNA species from spores and the asporogenous mutant in stationary phase both exhibited altered chromatographic profiles compared to that of log-phase cells. The major peak in spore lysyl-tRNA species eluted later than that characteristic of vegetative cells, whereas the major peak of the lysyl-tRNA species from the asporogenous mutant in stationary phase eluted earlier. Although the early eluting lysyl-tRNA species was observable on methylated albumin columns, the late eluting peak was not detectable by that column technique. By using a shallower gradient on an RPC-2 column, the resolution of all lysyl-tRNA species increased. Several subspecies were revealed. The chromatographic comparisons clearly show that both the spore-forming strain and the asporogenous mutant undergo relative increases in different lysyl-tRNA species when grown to late stationary phase. No new species seem to be involved but rather altered amounts of minor species existing in log-phase cells. The experiments also demonstrate the usefulness of reversed-phase columns for such comparisons.

MeSH Terms
Albumins Bacillus subtilis/analysis,growth & development,metabolism Carbon Isotopes Chromatography Genetics, Microbial Lysine/metabolism Methods Mutation RNA, Bacterial/analysis,isolation & purification RNA, Transfer/analysis,isolation & purification Silicon Dioxide Species Specificity Spectrophotometry Spores/analysis,growth & development,metabolism Tritium
Chemicals
Albumins Carbon Isotopes RNA, Bacterial Tritium Silicon Dioxide RNA, Transfer Lysine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Vold B S
References (8)
8 references, click to expand
  1. Alteration of valyl-sRNA during sporulation of bacillus subtilis.
    Proc Natl Acad Sci U S A. 1966 Mar;55(3):564-71 PMID: 4957526
  2. Differences in lysine-sRNA from spore and vegetative cells of Bacillus subtillis.
    Proc Natl Acad Sci U S A. 1966 Jul;56(1):185-90 PMID: 4961191
  3. Medium-dependent alteration of lysine transfer ribonucleic acid in sporulating Bacillus subtilis cells.
    J Bacteriol. 1967 Jul;94(1):125-30 PMID: 4961410
  4. A new chromatographic system for increased resolution of transfer ribonucleic acids.
    Biochemistry. 1967 Aug;6(8):2507-13 PMID: 4862273
  5. Isolation and properties of undermethylated phenylalanine transfer ribonucleic acids from a relaxed mutant of Escherichia coli.
    Biochim Biophys Acta. 1968 Mar 18;157(1):83-90 PMID: 4868251
  6. Role modifications in tyrosine transfer RNA: a modified base affecting ribosome binding.
    J Mol Biol. 1969 Jan 14;39(1):145-57 PMID: 4938812
  7. A fractionating column for analysis of nucleic acids.
    Anal Biochem. 1960 Jun;1:66-77 PMID: 14420563
  8. THE CHARACTERIZATION OF A NEW SPECIES OF LEUCYL-SRNA FORMED DURING METHIONINE DEPRIVATION OF ESCHERICHIA COLI WITH RELAXED CONTROL.
    Proc Natl Acad Sci U S A. 1965 Mar;53:549-56 PMID: 14338234
Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1970-06-00
Pages
711-5
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC247616
Subset
IM
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