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Fungal 17 beta-hydroxysteroid dehydrogenase.
T Lanisnik1, M Zakelj-Mavric, I Belic
1Institute of Biochemistry, Medical Faculty, University of Ljubljana, Slovenia.
FEMS Microbiology Letters
|November 15, 1992
Summary
Fungal steroid metabolism involves 17 beta-hydroxysteroid dehydrogenase (HSDH) enzymes, found in all tested species. These enzymes primarily act on the C17 steroid position, with oxidative pathways often preferred.
Area of Science:
- Mycology
- Biochemistry
- Enzymology
Background:
- Steroid metabolism is crucial in many organisms.
- Hydroxysteroid dehydrogenases (HSDHs) play key roles in steroid transformations.
- Fungal HSDH activity and its specific roles remain underexplored.
Purpose of the Study:
- To investigate the presence and characteristics of 17 beta-hydroxysteroid dehydrogenase (HSDH) activity in diverse fungal species.
- To determine the regioselectivity and pathway preference (oxidative vs. reductive) of fungal HSDHs.
- To explore the potential ecological or metabolic significance of HSDH in fungi.
Main Methods:
- Testing constitutive 17 beta-HSDH activity in fungal isolates from various taxonomic classes.
- Assessing enzyme regioselectivity for the C17 position of steroid substrates.
- Detecting 20 beta-HSDH activity in specific fungal strains.
- Comparing the rates of oxidative and reductive pathways catalyzed by the enzyme.
Main Results:
- Constitutive 17 beta-HSDH activity was detected in all tested fungal representatives across different classes.
- The enzyme exhibited regioselectivity for the C17 position of the steroid ring.
- 20 beta-HSDH activity was specifically identified in *Trichoderma viride*.
- The oxidative pathway was favored over the reductive pathway in most fungal species examined.
Conclusions:
- Fungi possess widespread 17 beta-HSDH activity, suggesting a conserved role in steroid processing.
- Fungal HSDHs are primarily C17-acting enzymes, with potential for specific isoforms like 20 beta-HSDH.
- The prevalence of the oxidative pathway indicates its importance in fungal steroid biotransformation.