Anaerobic Conditioning of E. coli Cell Lysate for Enhanced In Vitro Protein Synthesis

被引:5
作者
Tamiev, Denis [1 ]
Dopp, Jared L. [2 ]
Reuel, Nigel F. [2 ]
机构
[1] Iowa State Univ, Biochem Biophys & Mol Biol Dept, Ames, IA 50011 USA
[2] Iowa State Univ, Chem & Biol Engn Dept, Ames, IA 50011 USA
关键词
NITRITE REDUCTION; ESCHERICHIA-COLI; AMMONIA; SYSTEM;
D O I
10.1021/acssynbio.0c00501
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cell-free protein expression (CFPS) from E. coli cell lysate is an established chemical biology technique. Common efforts to improve synthesis capacity, such as strain engineering and process improvements, have overlooked the opportunity to increase productivity by reducing the dependence on limited, dissolved oxygen. Here we demonstrate conditioning E. coli cells for anaerobic respiration which increases the initial protein expression rate up to 4-fold and increases titer by 50% as compared to traditional aerobic cell lysate when using sfGFP as a reporter protein in CFPS reactions run at atmospheric conditions. This enhancement is even more significant when run in an oxygen-depleted environment, where anaerobic respiration preconditioned cells increase yield when supplemented with nitrite as a terminal electron acceptor (TEA). Furthermore, we test knockout mutants to determine key proteins responsible for enhancing the anaerobically prepared CFPS lysate. Further improvements could be made in preconditioning cells by increasing expression levels of critical pathway enzymes or by screening other TEA.
引用
收藏
页码:716 / 723
页数:8
相关论文
共 31 条
[1]  
ASAKURA T, 1978, J BIOL CHEM, V253, P6423
[2]   Cell-free synthesis and maturation of [FeFe] hydrogenases [J].
Boyer, Marcus E. ;
Stapleton, James A. ;
Kuchenreuther, Jon M. ;
Wang, Chia-Wei ;
Swartz, James R. .
BIOTECHNOLOGY AND BIOENGINEERING, 2008, 99 (01) :59-67
[3]  
COLE JA, 1978, FEMS MICROBIOL LETT, V4, P327
[4]   NITRITE REDUCTION TO AMMONIA BY FERMENTATIVE BACTERIA - SHORT-CIRCUIT IN THE BIOLOGICAL NITROGEN-CYCLE [J].
COLE, JA ;
BROWN, CM .
FEMS MICROBIOLOGY LETTERS, 1980, 7 (02) :65-72
[5]   Methodologies for preparation of prokaryotic extracts for cell-free expression systems [J].
Cole, Stephanie D. ;
Miklos, Aleksandr E. ;
Chiao, Abel C. ;
Sun, Zachary Z. ;
Lux, Matthew W. .
SYNTHETIC AND SYSTEMS BIOTECHNOLOGY, 2020, 5 (04) :252-267
[6]   Holistic engineering of cell-free systems through proteome-reprogramming synthetic circuits [J].
Contreras-Llano, Luis E. ;
Meyer, Conary ;
Liu, Yao ;
Sarker, Mridul ;
Lim, Sierin ;
Longo, Marjorie L. ;
Tan, Cheemeng .
NATURE COMMUNICATIONS, 2020, 11 (01)
[7]   Simple, functional, inexpensive cell extract for in vitro prototyping of proteins with disulfide bonds [J].
Dopp, Jared L. ;
Reuel, Nigel F. .
BIOCHEMICAL ENGINEERING JOURNAL, 2020, 164
[8]   Methods to reduce variability in E. Coli-based cell-free protein expression experiments [J].
Dopp, Jared L. ;
Jo, Yeong Ran ;
Reuel, Nigel F. .
SYNTHETIC AND SYSTEMS BIOTECHNOLOGY, 2019, 4 (04) :204-211
[9]   Process optimization for scalable E.coli extract preparation for cell-free protein synthesis [J].
Dopp, Jared L. ;
Reuel, Nigel F. .
BIOCHEMICAL ENGINEERING JOURNAL, 2018, 138 :21-28
[10]   Rapid prototyping of proteins: Mail order gene fragments to assayable proteins within 24 hours [J].
Dopp, Jared Lynn ;
Rothstein, Samuel Michael ;
Mansell, Thomas Joseph ;
Reuel, Nigel Forest .
BIOTECHNOLOGY AND BIOENGINEERING, 2019, 116 (03) :667-676