Biotransformation of Hydrocortisone by Mucor hiemalis and In silico Study of the Produced Metabolite against 11β-Hydroxysteroid Dehydrogenase Type I.

Bahman Nickavar, Maryam Mehmannavaz
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引用次数: 0

Abstract

Background: Microbial biotransformation of steroids is a valuable method for producing active pharmaceuticals or potentially active steroids, and fungi serve as powerful biocatalysts in this process. On the other hand, in silico analyses are preliminary yet influential studies for the evaluation of compounds in the drug development process.

Objective: This study aimed to examine the ability of Mucor hiemalis to biotransform hydrocortisone, predict the potential binding ability of the products to the 11β- hydroxysteroid dehydrogenase enzyme (as a target for the control of diabetes mellitus type 2), and assess the products' pharmacokinetic properties.

Methods: The incubation of M. hiemalis with hydrocortisone for nine days resulted in the production of a main product in the culture medium. The metabolite was subsequently isolated using chromatographic procedures and its identity was determined by spectroscopic analysis. Computational binding studies and pharmacokinetic profile prediction of the metabolite were conducted using AutoDock Vina and SwissADME, respectively.

Results: The biotransformation of hydrocortisone by M. hiemalis produced 11β,17α,20β,21-tetrahydroxypregn-4-en-3-one as the major metabolite. Molecular docking studies demonstrated that the metabolite can interact with functional residues located at the catalytic site of the enzyme in different ways. Furthermore, the results indicated a favorable pharmacokinetic profile of the produced metabolite.

Conclusion: The current study showed that M. hiemalis may be considered an effective tool for the biotransformation of steroids and the production of potentially bioactive compounds.

毛霉对氢化可的松的生物转化及其对ⅰ型11β-羟基类固醇脱氢酶代谢产物的研究。
背景:微生物对类固醇的生物转化是生产活性药物或潜在活性类固醇的一种有价值的方法,真菌在这一过程中起着强有力的生物催化剂的作用。另一方面,在药物开发过程中,计算机分析对化合物的评价是初步的但有影响的研究。目的:研究毛霉对氢化可的松的生物转化能力,预测产物与11β-羟基类固醇脱氢酶(作为控制2型糖尿病的靶点)的潜在结合能力,并评价产物的药动学性质。方法:用氢化可的松培养hiemalis 9 d,在培养基中产生主要产物。代谢物随后用色谱方法分离,并通过光谱分析确定其身份。分别使用AutoDock Vina和SwissADME进行代谢物的计算结合研究和药代动力学谱预测。结果:M. hiemalis对氢化可的松的生物转化产生11β,17α,20β,21-四羟基孕酮-4-en-3-one为主要代谢物。分子对接研究表明,代谢物可以以不同的方式与酶催化位点的功能残基相互作用。此外,结果表明,产生的代谢物具有良好的药代动力学特征。结论:目前的研究表明,海马杆菌可能被认为是类固醇生物转化和生产潜在生物活性化合物的有效工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.60
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