An elevated OmpA expression during the production of a recombinant protein in Escherichia coli

被引:0
作者
Kurnia, Frans [1 ]
Novirani, Gestria [1 ]
Khairunnisa, Fatiha [1 ,2 ]
Meidianto, Vincencius F. [1 ]
Ismaya, Wangsa T. [1 ]
Tjandrawinata, Raymond R. [1 ,3 ]
机构
[1] PT Dexa Med, Dexa Labs Biomol Sci, Ind Selatan 5 Blok PP-7,Jababeka 2 Ind Estate, Cikarang 17550, Indonesia
[2] Airlangga Univ, Fac Sci & Technol, Dept Chem, Kampus C Mulyorejo, Surabaya 60115, Indonesia
[3] Atma Jaya Catholic Univ Indonesia, Fac Biotechnol, South Jakarta 12930, Indonesia
关键词
Escherichia coli; Fermentation; OmpA; Recombinant protein expression; Upscaling; MESSENGER-RNA STABILITY; OUTER-MEMBRANE; CYCLIC-AMP; GLUCOSE;
D O I
10.1007/s42770-023-01152-6
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Escherichia coli cells rapidly respond to changes in the environment. Such response must be anticipated upon development of fermentation strategy for commercial purposes. The response may signal changes in cell physiology, which is critical for the cell growth and the level of the target protein production. One of the responses is the elevated expression of membrane proteins to tightly control the trafficking of molecules into and out from the cells. Normally, the expression level of the membrane protein is basal as the fermentation is carried out in physiological conditions. Here, we reported an elevated expression of the outer membrane protein A (OmpA) during a series of fermentation conduct, starting from the shake flask, 1-L to finally 10-L fermentor. The incidence led to a lower expression of the target protein and thereby resulting in lower process efficiency. OmpA expression was concomitant to the bacterial growth and already observed in the early exponential phase. Despite the drawback, this phenomenon actually inspires the observation of OmpA expression as one of the indicators for the E. coli cells response to the fermentation conditions. This auxiliary check would prevent the higher OmpA expression that led to the low expression of the target protein.
引用
收藏
页码:2755 / 2763
页数:9
相关论文
共 50 条
[31]   Deleting mrdA and mrcB to significantly improve extracellular recombinant protein production in Escherichia coli [J].
Yang, Haiquan ;
Wang, Fuxiang ;
Wang, Haokun ;
Lu, Xiao ;
Shen, Wei ;
Chen, Xianzhong .
BIOCHEMICAL ENGINEERING JOURNAL, 2019, 143 :185-195
[32]   Strong stimulation of recombinant protein production in Escherichia coli by combining stimulatory control elements in an expression cassette [J].
Zwick, Friederike ;
Lale, Rahmi ;
Valla, Svein .
MICROBIAL CELL FACTORIES, 2012, 11
[33]   Strong stimulation of recombinant protein production in Escherichia coli by combining stimulatory control elements in an expression cassette [J].
Friederike Zwick ;
Rahmi Lale ;
Svein Valla .
Microbial Cell Factories, 11
[34]   The PAR promoter expression system: Modified lac promoters for controlled recombinant protein production in Escherichia coli [J].
Hothersall, Joanne ;
Godfrey, Rita E. ;
Fanitsios, Christos ;
Overton, Tim W. ;
Busby, Stephen J. W. ;
Browning, Douglas F. .
NEW BIOTECHNOLOGY, 2021, 64 :1-8
[35]   Production and Purification of Recombinant Proteins from Escherichia coli [J].
Tripathi, Nagesh K. .
CHEMBIOENG REVIEWS, 2016, 3 (03) :116-133
[36]   Engineering cell physiology to enhance recombinant protein production in Escherichia coli [J].
Chou, C. Perry .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2007, 76 (03) :521-532
[37]   Production of recombinant serpins in Escherichia coli [J].
Bird, PI ;
Pak, SC ;
Worrall, DM ;
Bottomley, SP .
METHODS, 2004, 32 (02) :169-176
[38]   Strategies to Enhance Periplasmic Recombinant Protein Production Yields in Escherichia coli [J].
Karyolaimos, Alexandros ;
de Gier, Jan-Willem .
FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY, 2021, 9
[39]   The production of polyhydroxyalkanoates in recombinant Escherichia coli [J].
Li, Rui ;
Zhang, Hanxing ;
Qi, Qingsheng .
BIORESOURCE TECHNOLOGY, 2007, 98 (12) :2313-2320
[40]   Butanol production from glycerol by recombinant Escherichia coli [J].
Zhou, Pengpeng ;
Zhang, Yan ;
Wang, Pixiang ;
Xie, Jingli ;
Ye, Qin .
ANNALS OF MICROBIOLOGY, 2014, 64 (01) :219-227