The inhibitory effect of cyclodextrin on the degradation of 9α-hydroxyandrost-4-ene-3,17-dione by Mycobacterium sp. VKM Ac-1817D

The inhibitory effect of methylated β-cyclodextrin (mCD) on steroid degradation was studied using the degradation of 9α-hydroxyandrost-4-ene-3,17-dione (9-OH-AD) by Mycobacterium sp. VKM Ac-1817D as a model process. The formation of the [9-OH-AD-mCD] complex was shown by 1 H NMR-spectroscopy. The bi...

Full description

Saved in:
Bibliographic Details
Published inBiocatalysis and biotransformation Vol. 25; no. 5; pp. 386 - 392
Main Authors Khomutov, Sergey M., Sukhodolskaya, Galina V., Donova, Marina V.
Format Journal Article
LanguageEnglish
Published Abingdon Taylor & Francis 01.01.2007
Taylor and Francis
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The inhibitory effect of methylated β-cyclodextrin (mCD) on steroid degradation was studied using the degradation of 9α-hydroxyandrost-4-ene-3,17-dione (9-OH-AD) by Mycobacterium sp. VKM Ac-1817D as a model process. The formation of the [9-OH-AD-mCD] complex was shown by 1 H NMR-spectroscopy. The biodegradation of 9-OH-AD by whole and disrupted cells was carried out at 30°C in aqueous solutions with or without mCD. Enzyme kinetic parameters were calculated by non-linear regression of the Michaelis-Menten plot. The complexation of 9-OH-AD and mCD was evaluated via the stability constant for the [9-OH-AD-mCD] complex. The V max and K M values calculated for the free (non-complex) steroid in mCD solutions corresponded to steroid degradation in the absence of mCD. The inclusion complex [9-OH-AD-mCD] was shown to be resistant to enzymatic degradation. The inference is made that the ''guest-host'' molecular complexation with cyclodextrin can be used for the control of steroid bioconversions.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1024-2422
1029-2446
DOI:10.1080/10242420701510510