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PMID: 4359918 Published · ppublish English Journal Article

The structure of novel C35 pentacyclic terpenes from Acetobacter xylinum.

The Biochemical journal ·Vol. 135 ·No. 1 ·1973-09-00 ·Pages 133-43

Förster HJ, Biemann K, Haigh WG, Tattrie NH, Colvin JR

Abstract

A novel C(35) terpene and its monounsaturated analogue were isolated from cultures of Acetobacter xylinum, together with traces of their C(36) homologues. These substances were found to be hopane derivatives substituted by a five-carbon chain bearing four vicinal hydroxyl groups. For the parent hydrocarbon the term bacteriohopane is proposed. The elucidation of the structures utilized high-resolution mass spectrometry of the terpenes, degradation to C(32) hydrocarbons and detailed mass-spectrometric comparison of these with C(32) hydrocarbons synthesized from known pentacyclic triterpenes. High-resolution mass-spectral data of the terpenes are presented. N.m.r. data are in agreement with the proposed structures, which are further supported by the isolation from the same organism of 22-hydroxyhopane and derivative hopene(s).

MeSH Terms
Chromatography, Gas Gluconacetobacter xylinus/analysis Magnetic Resonance Spectroscopy Mass Spectrometry Molecular Conformation Periodic Acid Terpenes/analysis,chemical synthesis
Chemicals
Terpenes Periodic Acid
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Förster H J
Biemann K
Haigh W G
Tattrie N H
Colvin J R
References (2)
2 references, click to expand
  1. Induction of orientation of bacterial cellulose microfibrils by a novel terpenoid from Acetobacter xylinum.
    Biochem J. 1973 Sep;135(1):145-9 PMID: 4776865
  2. A simple method for the isolation and purification of total lipides from animal tissues.
    J Biol Chem. 1957 May;226(1):497-509 PMID: 13428781
Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1973-09-00
Pages
133-43
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1165798
Subset
IM
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