Effect of gene knockouts of L-tryptophan uptake system on the production of L-tryptophan in Escherichia coli

被引:21
作者
Zhao, Zhijun [1 ,2 ,3 ]
Chen, Sheng [1 ,2 ,3 ]
Wu, Dan [1 ,2 ,3 ]
Wu, Jing [1 ,2 ,3 ]
Chen, Jian [1 ,2 ,3 ]
机构
[1] Jiangnan Univ, State Key Lab Food Sci & Technol, Wuxi 214122, Jiangsu, Peoples R China
[2] Jiangnan Univ, Minist Educ, Key Lab Ind Biotechnol, Wuxi 214122, Jiangsu, Peoples R China
[3] Jiangnan Univ, Sch Biotechnol, Wuxi 214122, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
L-Tryptophan; Uptake system; Gene knockout; Batch fermentation; Escherichia coli; CATABOLITE REPRESSION; AMINO-ACIDS; TRANSPORT; OPERON; HYPERPRODUCTION; OVERPRODUCTION; FERMENTATION; EXPRESSION; THREONINE; MUTANTS;
D O I
10.1016/j.procbio.2011.11.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Uptake of L-tryptophan in Escherichia coli was carried out by three distinct permeases, Mtr. TnaB, and AroP, respectively. In the present study, the three genes of L-tryptophan uptake system were knocked out from an L-tryptophan-producing strain of E. coli, respectively. The knockout mutants all showed lower L-tryptophan uptake activities and higher L-tryptophan production than their parent. Among the three genes, the knockout of mtr was most critical for both L-tryptophan uptake and L-tryptophan production. The uptake activity of L-tryptophan of the mtr mutant was 1.5 nmol min(-1) (mg dry weight)(-1), which was decreased by 48% when compared to that of the parent; the production of L-tryptophan of the mtr mutant was 14.7 g/l, which was increased by 34% when compared to that of the parent. Furthermore, the physiological and fermentation characteristics caused by gene knockouts were also analyzed. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:340 / 344
页数:5
相关论文
共 31 条
[1]  
[Anonymous], 2007, MICROBIOL MONOGR, DOI DOI 10.1007/7171_2006_069
[2]   HYPER-PRODUCTION OF L-TRYPTOPHAN VIA FERMENTATION WITH CRYSTALLIZATION [J].
AZUMA, S ;
TSUNEKAWA, H ;
OKABE, M ;
OKAMOTO, R ;
AIBA, S .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1993, 39 (4-5) :471-476
[3]   Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants:: the Keio collection [J].
Baba, Tomoya ;
Ara, Takeshi ;
Hasegawa, Miki ;
Takai, Yuki ;
Okumura, Yoshiko ;
Baba, Miki ;
Datsenko, Kirill A. ;
Tomita, Masaru ;
Wanner, Barry L. ;
Mori, Hirotada .
MOLECULAR SYSTEMS BIOLOGY, 2006, 2 (1) :2006.0008
[4]   Bacterial amino acid transport proteins:: occurrence, functions, and significance for biotechnological applications [J].
Burkovski, A ;
Krämer, R .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2002, 58 (03) :265-274
[5]   Interaction between lysine 102 and aspartate 338 in the insect amino acid cotransporter KAAT1 [J].
Castagna, M. ;
Soragna, A. ;
Mari, S. A. ;
Santacroce, M. ;
Bette, S. ;
Mandela, P. G. ;
Rudnick, G. ;
Peres, A. ;
Sacchi, V. F. .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2007, 293 (04) :C1286-C1295
[6]   AMPLIFICATION OF THE TRYPTOPHAN OPERON GENE IN ESCHERICHIA-COLI CHROMOSOME TO INCREASE L-TRYPTOPHAN BIOSYNTHESIS [J].
CHAN, EC ;
TSAI, HL ;
CHEN, SL ;
MOU, DG .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1993, 40 (2-3) :301-305
[7]   Potential of fermentation profiling via rapid measurement of amino acid metabolism by liquid chromatography-tandem mass spectrometry [J].
Dalluge, JJ ;
Smith, S ;
Sanchez-Riera, F ;
McGuire, C ;
Hobson, R .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1043 (01) :3-7
[8]   Optimization of the glucose feed rate profile for the production of tryptophan from recombinant E coli [J].
Dodge, TC ;
Gerstner, JM .
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2002, 77 (11) :1238-1245
[9]   YddG from Escherichia coli promotes export of aromatic amino acids [J].
Doroshenko, Vera ;
Airich, Larisa ;
Vitushkina, Maria ;
Kolokolova, Alexandra ;
Livshits, Vitaliy ;
Mashko, Sergey .
FEMS MICROBIOLOGY LETTERS, 2007, 275 (02) :312-318
[10]   CATABOLITE REPRESSION IN ESCHERICHIA-COLI MUTANTS LACKING CYCLIC-AMP RECEPTOR PROTEIN [J].
GUIDIRONTANI, C ;
DANCHIN, A ;
ULLMANN, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (10) :5799-5801