前往化源商城

Bioresource Technology 2014-12-01

Bioreduction of α,β-unsaturated ketones and aldehydes by non-conventional yeast (NCY) whole-cells.

Matthew E Kutcher, Lucy Z Kornblith, Ryan F Vilardi, Brittney J Redick, Mary F Nelson, Mitchell Jay Cohen

文献索引:Bioresour. Technol. 102(5) , 3993-8, (2011)

全文:HTML全文

摘要

The bioreduction of α,β-unsaturated ketones (ketoisophorone, 2-methyl- and 3-methyl-cyclopentenone) and aldehydes [(S)-(-)-perillaldehyde and α-methyl-cinnamaldehyde] by 23 "non-conventional" yeasts (NCYs) belonging to 21 species of the genera Candida, Cryptococcus, Debaryomyces, Hanseniaspora, Kazachstania, Kluyveromyces, Lindnera, Nakaseomyces, Vanderwaltozyma, and Wickerhamomyces was reported. The results highlight the potential of NCYs as whole-cell biocatalysts for selective biotransformation of electron-poor alkenes. A few NCYs exhibited extremely high (>90%) or even total ketoisophorone and 2-methyl-cyclopentenone bioconversion yields via asymmetric reduction of the conjugated CC bond catalyzed by enoate reductases. Catalytic efficiency declined after switching from ketones to aldehydes. High chemoselectivity due to low competing carbonyl reductases was also sometimes observed.Copyright © 2010 Elsevier Ltd. All rights reserved.

相关化合物

结构式 名称/CAS号 全部文献
环戊酮 结构式 环戊酮
CAS:120-92-3
茶香酮 结构式 茶香酮
CAS:1125-21-9