Searching for the physiological function of 17 beta-hydroxysteroid dehydrogenase from the fungus Cochliobulus lunatus: studies of substrate specificity and expression analysis
Tl. Rizner et al., Searching for the physiological function of 17 beta-hydroxysteroid dehydrogenase from the fungus Cochliobulus lunatus: studies of substrate specificity and expression analysis, MOL C ENDOC, 171(1-2), 2001, pp. 193-198
17 beta -hydroxysteroid dehydrogenase from the filamentous fungus Cochliobo
lus lunatus (17 beta -HSDcl) has recently been characterized. Since its fun
ction is still unclear, we performed substrate specificity studies to obtai
n some indications about its physiological function. Different steroids wer
e studied as putative substrates of recombinant 17 beta -HSDcl, androgens a
nd estrogens, brassinosteroids, and the fungal steroid herbarulid. Among th
ese androgens and estrogens were most efficiently converted. The Following
substrates in decreasing order were best reduced: 4-estrene-3,17-dione, 5 a
lpha -androstane-3,17-dione, 4-androstene-3,17-dione and estrone. Two typic
al inhibitors were tested: carbenoxolone - a representative inhibitor of th
e SDR family and quercetin - a diagnostic inhibitor of carbonyl reductases.
Among these two quercetin was more efficient. Expression studies revealed
that 17 beta -HSDcl is mainly expressed in the stationary phase of growth i
ndicating its possible involvement in secondary metabolism. (C) 2001 Elsevi
er Science Ireland Ltd. All rights reserved.