2021
DOI: 10.1039/d1ra02774c
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Identification and in situ removal of an inhibitory intermediate to develop an efficient phytosterol bioconversion process using a cyclodextrin-resting cell system

Abstract: We identified an inhibitory intermediate, 4-ene-3-keto steroids, that limits the bioconversion rate and provided a solution based on resin adsorption for improving 9α-OH-AD production efficiency in a commercial-scale process.

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Cited by 7 publications
(3 citation statements)
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“…The in-depth influence of detergents on the synthesis of steroids at the metabolic level is worth exploring. In addition to these results, propionyl-CoA, ROS, and 4-ene-3-ketosteroids were identified as toxic molecules that inhibit the synthesis of 9α-OH-AD, and an in-situ adsorption scheme improved the production efficiency by 23.15% (Wang et al 2021 ). Development of omics not only rapidly promoted the technological development of the biosynthesis of steroids, but also provided genetic data for constructing efficient pathways and designing biological cell factories.…”
Section: Significance Of Monooxygenase Resources For Steroid Modifica...mentioning
confidence: 98%
“…The in-depth influence of detergents on the synthesis of steroids at the metabolic level is worth exploring. In addition to these results, propionyl-CoA, ROS, and 4-ene-3-ketosteroids were identified as toxic molecules that inhibit the synthesis of 9α-OH-AD, and an in-situ adsorption scheme improved the production efficiency by 23.15% (Wang et al 2021 ). Development of omics not only rapidly promoted the technological development of the biosynthesis of steroids, but also provided genetic data for constructing efficient pathways and designing biological cell factories.…”
Section: Significance Of Monooxygenase Resources For Steroid Modifica...mentioning
confidence: 98%
“…In Actinobacteria, the degradation of sterols begins with the oxidation of the β-hydroxyl group of cholesterol, catalyzed by either cholesterol oxidase (ChO) or 3-hydroxysteroid dehydrogenase (3-HSD), leading to the formation of cholest-4-en-3-one (Figure 3) [58][59][60]. Subsequently, through the combined action of 3-ketosteroid-∆1-dehydrogenase (KstD) and 3-sterone-9α-hydroxylase (Ksh), the B-ring of the steroid nucleus undergoes cleavage, eventually resulting in the degradation of products into short-chain organic molecules like propionyl-CoA and propionate [50,61].…”
Section: Reconstructing the Degradation Pathway Of Steroid Nucleusmentioning
confidence: 99%
“…However, with the further increase of SSL, the yields decreased; and no ADD was generated when the ratio of SSL/phytosterols reached 4:1. Hence, SSL as co-solvent could not enhance the ADD biosynthesis of the perlite-immobilized M. neoaurum R. Resins were employed as adsorbents for steroids in several researches on steroid biotransformation (Molchanova et al 2007;Wang et al 2021). In fermentation medium containing the equal amount of macroporous resin HPD826 as phytosterols, ADD reached 1.11 g/L, which was 60.9% higher than that in media without HPD826.…”
Section: Optimization Of Add Accumulation By Immobilized M Neoaurum Rmentioning
confidence: 99%