Production of γ-decalactone and 4-hydroxy-decanoic acid in the genus Sporidiobolus

Within the genus Sporidiobolus, S. odorus has been widely reported as having the ability to convert castor oil or its derivatives to γ-decalactone, but other species have also shown potential for lactone production. In this work, the bioconversion of ricinoleic acid methyl ester to γ-decalactone was...

Full description

Saved in:
Bibliographic Details
Published inJournal of fermentation and bioengineering Vol. 86; no. 2; pp. 169 - 173
Main Authors Dufossé, Laurent, Feron, Gilles, Mauvais, Geneviève, Bonnarme, Pascal, Durand, Alain, Spinnler, Henry-Eric
Format Journal Article
LanguageEnglish
Published Osaka Elsevier B.V 01.01.1998
Society for Fermentation and Bioengineering
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Within the genus Sporidiobolus, S. odorus has been widely reported as having the ability to convert castor oil or its derivatives to γ-decalactone, but other species have also shown potential for lactone production. In this work, the bioconversion of ricinoleic acid methyl ester to γ-decalactone was studied with four species of Sporidiobolus: S. salmonicolor, S. ruinenii, S. johnsonii, and S. pararoseus. With 4.1 g/ l of ricinoleic acid methyl ester, only S. salmonicolor and S. ruinenii were able to produce γ-decalactone (12 and 40 mg/ l respectively). S. johnsonii and S. pararoseus did not produce any lactone in spite of consuming the precursor. The four strains showed different sensitivities to lactone. Between S. salmonicolor and S. ruinenii, the latter was the best biocatalyst. During four successive batch cultivations in a 7- l bioreactor, 5.5 g/ l of γ-decalactone was produced with S. ruinenii in each 10-d run. This was essentially due to its ability to produce the open form of γ-decalactone ( i.e., 4-hydroxy-decanoic acid), which is far less toxic than the lactone.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0922-338X
DOI:10.1016/S0922-338X(98)80056-1