Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1992 Jun 15;284(Pt 3):741–747. doi: 10.1042/bj2840741

Novel linear and branched polyamines in the extremely thermophilic eubacteria Thermoleophilum, Bacillus and Hydrogenobacter.

K Hamana 1, M Niitsu 1, S Matsuzaki 1, K Samejima 1, Y Igarashi 1, T Kodama 1
PMCID: PMC1132601  PMID: 1622392

Abstract

Novel tertiary branched tetra-amines, quaternary branched penta-amines, linear penta-amines and linear hexa-amines were distributed as the major polyamines in six obligately extremely thermophilic eubacteria belonging to Thermoleophilum, Bacillus or Hydrogenobacter. The major polyamine of Thermoleophilum album and Thermoleophilum minutum was identified as a quaternary branched penta-amine, 4,4-bis(3-aminopropyl)-1,8-diamino-4-azaoctane (NH2[CH2]3N+([CH2]3NH2)2[CH2]4NH2) by h.p.l.c., t.l.c. and g.c.-m.s. Hydrogenobacter thermophilus and Hydrogenobacter halophilus contained another quaternary branched penta-amine, 4,4-bis(3-aminopropyl)-1,7-diamino-4-azaheptane (NH2[CH2]3N([CH2]3NH2)2[CH2]3NH2) as the major polyamine, and tertiary branched tetra-amines (4-(3-aminopropyl)-1,7-diamino-4-azaheptane (NH2[CH2]3N([CH2]3NH2)[CH2]3NH2), 4-(3-aminopropyl)-1,8-diamino-4-azaoctane (NH2[CH2]3N([CH2]3NH2)[CH2]4NH2)) and 4,4-bis(3-aminopropyl)-1,8-diamino-4-azaoctane were confirmed as minor components. Bacillus schlegelii contained a branched tetra-amine, 4-(3-aminopropyl)-1,8-diamino-4-azaoctane, a branched penta-amine, 4,4-bis(3-aminopropyl)-1,8-diamino-4-azaoctane, a linear penta-amine, 1,16-diamino-4,8,13-triazahexadecane (NH2[CH2]3NH[CH2]3NH[CH2]4NH[CH2]3NH2) and linear hexa-amine(s), 1,20-diamino-4,8,12,17-tetra-azaeicosane (NH2[CH2]3NH[CH2]3NH[CH2]3NH[CH2]4NH[CH2]3NH2 ) and/or 1,20-diamino-4,8,13,17-tetra-azaeicosane (NH2[CH2]3NH[CH2]3NH[CH2]4NH[CH2]3NH[CH2]3NH2 ).

Full text

PDF
741

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Hamana K., Akiba T., Uchino F., Matsuzaki S. Distribution of spermine in bacilli and lactic acid bacteria. Can J Microbiol. 1989 Apr;35(4):450–455. doi: 10.1139/m89-069. [DOI] [PubMed] [Google Scholar]
  2. Hamana K., Matsuzaki S. Unusual polyamines in slime molds Physarum polycephalum and Dictyostelium discoideum. J Biochem. 1984 Apr;95(4):1105–1110. doi: 10.1093/oxfordjournals.jbchem.a134698. [DOI] [PubMed] [Google Scholar]
  3. Hamana K., Niitsu M., Samejima K., Matsuzaki S. Polyamine distributions in thermophilic eubacteria belonging to Thermus and Acidothermus. J Biochem. 1991 Mar;109(3):444–449. doi: 10.1093/oxfordjournals.jbchem.a123401. [DOI] [PubMed] [Google Scholar]
  4. Matsuzaki S., Hamana K., Imai K., Matsuura K. Occurrence in high concentrations of N1-acetylspermidine and syn-homospermidine in the hamster epididymis. Biochem Biophys Res Commun. 1982 Jul 16;107(1):307–313. doi: 10.1016/0006-291x(82)91705-3. [DOI] [PubMed] [Google Scholar]
  5. Matsuzaki S., Xiao L. P., Suzuki M., Hamana K., Niitsu M., Samejima K. Occurrence of aminopropylhomospermidine and canavalmine in the hamster epididymis. Biochem Int. 1987 Oct;15(4):817–822. [PubMed] [Google Scholar]
  6. Oshima T. A pentaamine is present in an extreme thermophile. J Biol Chem. 1982 Sep 10;257(17):9913–9914. [PubMed] [Google Scholar]
  7. Oshima T., Hamasaki N., Senshu M., Kakinuma K., Kuwajima I. A new naturally occurring polyamine containing a quaternary ammonium nitrogen. J Biol Chem. 1987 Sep 5;262(25):11979–11981. [PubMed] [Google Scholar]
  8. Oshima T., Kawahata S. Homocaldopentamine: a new naturally occurring pentaamine. J Biochem. 1983 May;93(5):1455–1456. doi: 10.1093/oxfordjournals.jbchem.a134281. [DOI] [PubMed] [Google Scholar]
  9. Stevens L., Morrison M. R. Studies on the role of polyamines associated with the ribosomes from Bacillus stearothermophilus. Biochem J. 1968 Jul;108(4):633–640. doi: 10.1042/bj1080633. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES