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Homofermentative production of optically pure L-lactic acid from xylose by genetically engineered Escherichia coli B

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    • 바이오플라스틱
      1. 플라스틱
    • 바이오정밀화학
      1. 기타
    • 화장품용 기능성소재
      1. 계면활성제⁄증점제
    • 의료용 화학소재
      1. 치료제
      2. 식품첨가제
논문

Homofermentative production of optically pure L-lactic acid from xylose by genetically engineered Escherichia coli B

학술지

Microbial cell factories

저자명

Zhao, Jinfang; Xu, Liyuan; Wang, Yongze; Zhao, Xiao; Wang, Jinhua; Garza, Erin; Manow, Ryan; Zhou, Shengde

초록

<P><B>Background</B></P><P>Polylactic acid (PLA), a biodegradable polymer, has the potential to replace (at least partially) traditional petroleum-based plastics, minimizing “white pollution”. However, cost-effective production of optically pure L-lactic acid is needed to achieve the full potential of PLA. Currently, starch-based glucose is used for L-lactic acid fermentation by lactic acid bacteria. Due to its competition with food resources, an alternative non-food substrate such as cellulosic biomass is needed for L-lactic acid fermentation. Nevertheless, the substrate (sugar stream) derived from cellulosic biomass contains significant amounts of xylose, which is unfermentable by most lactic acid bacteria. However, the microorganisms that do ferment xylose usually carry out heterolactic acid fermentation. As a result, an alternative strain should be developed for homofermentative production of optically pure L-lactic acid using cellulosic biomass.</P><P><B>Results</B></P><P>In this study, an ethanologenic <I>Escherichia coli</I> strain, SZ470 (&Delta;<I>frdBC</I> &Delta;<I>ldhA</I> &Delta;<I>ackA</I> &Delta;<I>pflB</I> &Delta;<I>pdhR ::pflBp6-acEF-lpd</I> &Delta;<I>mgsA)</I>, was reengineered for homofermentative production of L-lactic acid from xylose (1.2 mole xylose = > 2 mole L-lactic acid), by deleting the alcohol dehydrogenase gene (<I>adhE</I>) and integrating the L-lactate dehydrogenase gene (<I>ldhL</I>) of <I>Pediococcus acidilactici</I>. The resulting strain, WL203, was metabolically evolved further through serial transfers in screw-cap tubes containing xylose, resulting in the strain WL204 with improved anaerobic cell growth. When tested in 70 g L<SUP>-1</SUP> xylose fermentation (complex medium), WL204 produced 62 g L<SUP>-1</SUP> L-lactic acid, with a maximum production rate of 1.631 g L<SUP>-1</SUP> h<SUP>-1</SUP> and a yield of 97% based on xylose metabolized. HPLC analysis using a chiral column showed that an L-lactic acid optical purity of 99.5% was achieved by WL204.</P><P><B>Conclusions</B></P><P>These results demonstrated that WL204 has the potential for homofermentative production of L-lactic acid using cellulosic biomass derived substrates, which contain a significant amount of xylose.</P>

발행연도

2013

발행기관

BioMed Central

라이선스

cc-by

ISSN

1475-2859

12

페이지

pp.57-57

주제어

E. coli; Genetic engineering; L-lactic acid; PLA; Xylose fermentation

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논문; 2013-06-07

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