Application of microbial 3-ketosteroid Δ1-dehydrogenases in biotechnology

酮甾体 辅因子 脱氢酶 生物化学 化学 代谢工程 生物转化 生物过程 异构酶 生物 古生物学
作者
Ali Rohman,Bauke W. Dijkstra
出处
期刊:Biotechnology Advances [Elsevier BV]
卷期号:49: 107751-107751 被引量:29
标识
DOI:10.1016/j.biotechadv.2021.107751
摘要

3-Ketosteroid Δ1-dehydrogenase catalyzes the 1(2)-dehydrogenation of 3-ketosteroid substrates using flavin adenine dinucleotide as a cofactor. The enzyme plays a crucial role in microbial steroid degradation, both under aerobic and anaerobic conditions, by initiating the opening of the steroid nucleus. Indeed, many microorganisms are known to possess one or more 3-ketosteroid Δ1-dehydrogenases. In the pharmaceutical industry, 3-ketosteroid Δ1-dehydrogenase activity is exploited to produce Δ1-3-ketosteroids, a class of steroids that display various biological activities. Many of them are used as active pharmaceutical ingredients in drug products, or as key precursors to produce pharmaceutically important steroids. Since 3-ketosteroid Δ1-dehydrogenase activity requires electron acceptors, among other considerations, Δ1-3-ketosteroid production has been industrially implemented using whole-cell fermentation with growing or metabolically active resting cells, in which the electron acceptors are available, rather than using the isolated enzyme. In this review we discuss biotechnological applications of microbial 3-ketosteroid Δ1-dehydrogenases, covering commonly used steroid-1(2)-dehydrogenating microorganisms, the bioprocess for preparing Δ1-3-ketosteroids, genetic engineering of 3-ketosteroid Δ1-dehydrogenases and related genes for constructing new, productive industrial strains, and microbial fermentation strategies for enhancing the product yield. Furthermore, we also highlight the recent development in the use of isolated 3-ketosteroid Δ1-dehydrogenases combined with a FAD cofactor regeneration system. Finally, in a somewhat different context, we summarize the role of 3-ketosteroid Δ1-dehydrogenase in cholesterol degradation by Mycobacterium tuberculosis and other mycobacteria. Because the enzyme is essential for the pathogenicity of these organisms, it may be a potential target for drug development to combat mycobacterial infections.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
可爱的函函应助111采纳,获得10
1秒前
平淡的之云完成签到,获得积分20
1秒前
1秒前
yys发布了新的文献求助10
2秒前
八点必起发布了新的文献求助30
2秒前
5秒前
搞怪莫茗发布了新的文献求助10
5秒前
6秒前
6秒前
7秒前
bkagyin应助花花采纳,获得10
7秒前
8秒前
aaaa完成签到,获得积分10
9秒前
Anderson732发布了新的文献求助10
9秒前
兔子胡萝卜完成签到,获得积分10
10秒前
11秒前
12秒前
果汁羊排发布了新的文献求助10
12秒前
zfg完成签到,获得积分10
12秒前
13秒前
xjcy应助霸霸采纳,获得10
13秒前
14秒前
pxptmac发布了新的文献求助10
14秒前
15秒前
15秒前
深情安青应助pililili采纳,获得10
15秒前
wmy发布了新的文献求助10
16秒前
南柯一梦完成签到,获得积分10
16秒前
17秒前
17秒前
杨文琪发布了新的文献求助10
17秒前
18秒前
18秒前
蓝天发布了新的文献求助10
19秒前
852应助我不吃牛肉采纳,获得10
19秒前
123发布了新的文献求助10
19秒前
无极微光应助我不吃牛肉采纳,获得20
19秒前
天天快乐应助我不吃牛肉采纳,获得10
20秒前
20秒前
无极微光应助我不吃牛肉采纳,获得20
20秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Environmental Leverage in Times of Climate Crisis: Product Standards, Carbon Border Measures and Preferential Trade Agreements 1000
Erwählung und Berufung bei Paulus: Bedeutung, Entwicklung und Funktion einer Vorstellung in ihrem frühjüdischen und griechisch-römischen Kontext 850
Matrix Methods in Data Mining and Pattern Recognition 510
Structural Geology: A Quantitative Introduction 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7216639
求助须知:如何正确求助?哪些是违规求助? 8848176
关于积分的说明 18672361
捐赠科研通 6872864
什么是DOI,文献DOI怎么找? 3185098
关于科研通互助平台的介绍 2346933
邀请新用户注册赠送积分活动 2159383