Overcoming acetate in Escherichia coli recombinant protein fermentations

被引:311
作者
Eiteman, Mark A. [1 ]
Altman, Elliot [1 ]
机构
[1] Univ Georgia, Ctr Mol Bioengn, Athens, GA 30602 USA
关键词
D O I
10.1016/j.tibtech.2006.09.001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Escherichia, coli is the organism of choice for the expression of a wide variety of recombinant proteins for therapeutic, diagnostic and industrial applications. E. coli generates acetic acid (acetate) as an undesirable by-product that has several negative effects on protein production. Various strategies have been developed to limit acetate accumulation or reduce its negative effects to increase the productivity of recombinant proteins. This article reviews recent strategies for reducing or eliminating acetate, including approaches that optimize the protein production process as well as those that involve modifying the host organism itself.
引用
收藏
页码:530 / 536
页数:7
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共 74 条
[1]  
Åkesson M, 1999, BIOTECHNOL BIOENG, V64, P590, DOI 10.1002/(SICI)1097-0290(19990905)64:5<590::AID-BIT9>3.0.CO
[2]  
2-T
[3]   Avoiding acetate accumulation in Escherichia coli cultures using feedback control of glucose feeding [J].
Åkesson, M ;
Hagander, P ;
Axelsson, JP .
BIOTECHNOLOGY AND BIOENGINEERING, 2001, 73 (03) :223-230
[4]   ARE GROWTH-RATES OF ESCHERICHIA-COLI IN BATCH CULTURES LIMITED BY RESPIRATION [J].
ANDERSEN, KB ;
VONMEYENBURG, K .
JOURNAL OF BACTERIOLOGY, 1980, 144 (01) :114-123
[5]   Prokaryotic expression of antibodies [J].
Arbabi-Ghahroudi, M ;
Tanha, J ;
MacKenzie, R .
CANCER AND METASTASIS REVIEWS, 2005, 24 (04) :501-519
[6]   METABOLIC ENGINEERING OF ESCHERICHIA-COLI TO ENHANCE RECOMBINANT PROTEIN-PRODUCTION THROUGH ACETATE REDUCTION [J].
ARISTIDOU, AA ;
SAN, KY ;
BENNETT, GN .
BIOTECHNOLOGY PROGRESS, 1995, 11 (04) :475-478
[7]   Improvement of biomass yield and recombinant gene expression in Escherichia coli by using fructose as the primary carbon source [J].
Aristidou, AA ;
San, KY ;
Bennett, GN .
BIOTECHNOLOGY PROGRESS, 1999, 15 (01) :140-145
[8]   Global analysis of Escherichia coli gene expression during the acetate-induced acid tolerance response [J].
Arnold, CN ;
McElhanon, J ;
Lee, A ;
Leonhart, R ;
Siegele, DA .
JOURNAL OF BACTERIOLOGY, 2001, 183 (07) :2178-2186
[9]   Production of interferon-α in high cell density cultures of recombinant Escherichia coli and its single step purification from refolded inclusion body proteins [J].
Babu, KR ;
Swaminathan, S ;
Marten, S ;
Khanna, N ;
Rinas, U .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2000, 53 (06) :655-660
[10]   IMPROVED EXPRESSION OF HUMAN INTERLEUKIN-2 IN HIGH-CELL-DENSITY FERMENTER CULTURES OF ESCHERICHIA-COLI K-12 BY A PHOSPHOTRANSACETYLASE MUTANT [J].
BAUER, KA ;
BENBASSAT, A ;
DAWSON, M ;
DELAPUENTE, VT ;
NEWAY, JO .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1990, 56 (05) :1296-1302