Monocarboxylic acids from oxidation of acyclic isoprenoid alkanes by Mycobacterium fortuitum.

Abstract:

:Mycobacterium fortuitum utilizes certain stereoisometric mixtures of individual multimethyl branched alkanes as sole carbon source, including 2,6(R), 10(S), 14(RS)-tetramethylhexadecane; 2.6(R), 10(S), 14(RS)-tetramethylheptadecane; 2,6(RS), 10(RS)-trimethyltetradecane, and 2,6(R), 10(S)-trimethylpentadecane. Products of oxidation isolated from the bacterial lipids were acids derived predominantly from oxidation of the isopropyl terminus of each alkane, except in the case of 2,6(RS), 10(RS)-trimethyltetradecane. With the latter, acids from oxidation at either terminus were detected in comparable proportions.

journal_name

Lipids

journal_title

Lipids

authors

Cox RE,Maxwell JR,Myers RN

doi

10.1007/BF02532587

subject

Has Abstract

pub_date

1976-01-01 00:00:00

pages

72-6

issue

1

eissn

0024-4201

issn

1558-9307

journal_volume

11

pub_type

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