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Production of itaconate by whole-cell bioconversion of citrate mediated by expression of multiple cis-aconitate decarboxylase (cadA) genes in Escherichia coli

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논문

Production of itaconate by whole-cell bioconversion of citrate mediated by expression of multiple cis-aconitate decarboxylase (cadA) genes in Escherichia coli

학술지

Scientific reports

저자명

Kim, Junyoung; Seo, Hyung-Min; Bhatia, Shashi Kant; Song, Hun-Seok; Kim, Jung-Ho; Jeon, Jong-Min; Choi, Kwon-Young; Kim, Wooseong; Yoon, Jeong-Jun; Kim, Yun-Gon; Yang, Yung-Hun

초록

<P>Itaconate, a C<SUB>5</SUB> unsaturated dicarboxylic acid, is an important chemical building block that is used in manufacturing high-value products, such as latex and superabsorbent polymers. Itaconate is produced by fermentation of sugars by the filamentous fungus <I>Aspergillus terreus</I>. However, fermentation by <I>A. terreus</I> involves a long fermentation period and the formation of various byproducts, resulting in high production costs. <I>E. coli</I> has been developed as an alternative for producing itaconate. However, fermentation of glucose gives low conversion yields and low productivity. Here, we report the whole-cell bioconversion of citrate to itaconate with enhanced aconitase and cis-aconitate decarboxylase activities by controlling the expression of multiple <I>cadA</I> genes. In addition, this bioconversion system does not require the use of buffers, which reduces the production cost and the byproducts released during purification. Using this whole-cell bioconversion system, we were able to catalyze the conversion of 319.8 mM of itaconate (41.6 g/L) from 500 mM citrate without any buffer system or additional cofactors, with 64.0% conversion in 19 h and a productivity of 2.19 g/L/h. Our bioconversion system suggests very high productivity for itaconate production.</P>

발행연도

2017

발행기관

Nature Publishing Group

라이선스

cc-by

ISSN

2045-2322

7

페이지

pp.39768

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논문; 2017-01-04

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