Literature DB >> 16116273

Enhanced glutamic acid production by a H+-ATPase-defective mutant of Corynebacterium glutamicum.

Ryo Aoki1, Masaru Wada, Nobuchika Takesue, Kenji Tanaka, Atsushi Yokota.   

Abstract

Previously we reported that a mutant of Corynebacterium glutamicum ATCC14067 with reduced H+-ATPase activity, F172-8, showed an approximately two times higher specific rate of glucose consumption than the parent, but no glutamic acid productivity under the standard biotin-limited culture conditions, where biotin concentration was set at 5.5 microg/l in the production medium (Sekine et al., Appl. Microbiol. Biotechnol., 57, 534-540 (2001)). In this study, various culture conditions were tested to check the glutamic acid productivity of strain F172-8. The mutant was found to produce glutamic acid under exhaustive biotin limitation, where the biotin concentration of the medium was set at 2.5 microg/l with much smaller inoculum size. When strain F172-8 was cultured under the same biotin-limited conditions using a jar fermentor, 53.7 g/l of glutamic acid was produced from 100 g/l glucose, while the parent produced 34.9 g/l of glutamic acid in a medium with 5.5 microg/l biotin. The glutamic acid yield of strain F172-8 also increased under Tween 40-triggered production conditions (1.2-fold higher than the parent strain). The amounts of biotin-binding enzymes were investigated by Western blot analysis. As compared to the parent, the amount of pyruvate carboxylase was lower in the mutant; however, the amount of acetyl-CoA carboxylase did not significantly change under the glutamic acid production conditions. To the best of our knowledge, this is the first report showing that the H+-ATPase-defective mutant of C. glutamicum is useful in glutamic acid production.

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Year:  2005        PMID: 16116273     DOI: 10.1271/bbb.69.1466

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  6 in total

1.  Enhanced Glucose Consumption and Organic Acid Production by Engineered Corynebacterium glutamicum Based on Analysis of a pfkB1 Deletion Mutant.

Authors:  Satoshi Hasegawa; Yuya Tanaka; Masako Suda; Toru Jojima; Masayuki Inui
Journal:  Appl Environ Microbiol       Date:  2017-01-17       Impact factor: 4.792

2.  Platform engineering of Corynebacterium glutamicum with reduced pyruvate dehydrogenase complex activity for improved production of L-lysine, L-valine, and 2-ketoisovalerate.

Authors:  Jens Buchholz; Andreas Schwentner; Britta Brunnenkan; Christina Gabris; Simon Grimm; Robert Gerstmeir; Ralf Takors; Bernhard J Eikmanns; Bastian Blombach
Journal:  Appl Environ Microbiol       Date:  2013-07-08       Impact factor: 4.792

3.  Alterations of cellular physiology in Escherichia coli in response to oxidative phosphorylation impaired by defective F1-ATPase.

Authors:  Sakiko Noda; Yuji Takezawa; Tomohiko Mizutani; Tomoaki Asakura; Eiichiro Nishiumi; Kazunori Onoe; Masaru Wada; Fusao Tomita; Kazunobu Matsushita; Atsushi Yokota
Journal:  J Bacteriol       Date:  2006-10       Impact factor: 3.490

4.  Cofactor recycling for co-production of 1,3-propanediol and glutamate by metabolically engineered Corynebacterium glutamicum.

Authors:  Jinhai Huang; Yao Wu; Wenjun Wu; Ye Zhang; Dehua Liu; Zhen Chen
Journal:  Sci Rep       Date:  2017-02-08       Impact factor: 4.379

5.  Development and experimental verification of a genome-scale metabolic model for Corynebacterium glutamicum.

Authors:  Yohei Shinfuku; Natee Sorpitiporn; Masahiro Sono; Chikara Furusawa; Takashi Hirasawa; Hiroshi Shimizu
Journal:  Microb Cell Fact       Date:  2009-08-03       Impact factor: 5.328

Review 6.  Current advance in bioconversion of methanol to chemicals.

Authors:  Wenming Zhang; Meng Song; Qiao Yang; Zhongxue Dai; Shangjie Zhang; Fengxue Xin; Weiliang Dong; Jiangfeng Ma; Min Jiang
Journal:  Biotechnol Biofuels       Date:  2018-09-24       Impact factor: 6.040

  6 in total

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