Microbial dehydrogenation of a dithia-analogue of stearic acid
โ Scribed by Peter H. Buist; H.Garry Dallmann
- Book ID
- 104216363
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 262 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
The substitution of a methylene group by a sulfur atom at C-6 and C-13 of stearic acid does not prevent the bio-introduction of a cis -double bond between the two sulfur atoms.
Biological transformations of thia-analogues of fatty acids are being studied extensively in this laboratory.
๐ SIMILAR VOLUMES
Replacement of a methylene grouo by a sulfur atom at the 5-position of stearic acid does not prevent the introduction of a cis-double bond at the 9-,lO-positions. previous communication', we showed that an enzymatic methylating system was able to unactivated double bond in the presence of a more nu