Genetically encoded sensors enable real-time observation of metabolite production

被引:145
作者
Rogers, Jameson K. [1 ]
Church, George M. [1 ]
机构
[1] Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02115 USA
基金
美国国家科学基金会;
关键词
biotechnology; directed evolution; biosensor; metabolic engineering; synthetic biology; ESCHERICHIA-COLI; CHLOROFLEXUS-AURANTIACUS; 3-HYDROXYPROPIONIC ACID; SALMONELLA-ENTERICA; GLUCARIC ACID; E; COLI; EVOLUTION; EXPRESSION; TRANSCRIPTION; PRECISE;
D O I
10.1073/pnas.1600375113
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Engineering cells to produce valuable metabolic products is hindered by the slow and laborious methods available for evaluating product concentration. Consequently, many designs go unevaluated, and the dynamics of product formation over time go unobserved. In this work, we develop a framework for observing product formation in real time without the need for sample preparation or laborious analytical methods. We use genetically encoded biosensors derived from small-molecule responsive transcription factors to provide a fluorescent readout that is proportional to the intracellular concentration of a target metabolite. Combining an appropriate biosensor with cells designed to produce a metabolic product allows us to track product formation by observing fluorescence. With individual cells exhibiting fluorescent intensities proportional to the amount of metabolite they produce, high-throughput methods can be used to rank the quality of genetic variants or production conditions. We observe production of several renewable plastic precursors with fluorescent readouts and demonstrate that higher fluorescence is indeed an indicator of higher product titer. Using fluorescence as a guide, we identify process parameters that produce 3-hydroxypropionate at 4.2 g/L, 23-fold higher than previously reported. We also report, to our knowledge, the first engineered route from glucose to acrylate, a plastic precursor with global sales of $14 billion. Finally, we monitor the production of glucarate, a replacement for environmentally damaging detergents, and muconate, a renewable precursor to polyethylene terephthalate and nylon with combined markets of $51 billion, in real time, demonstrating that our method is applicable to a wide range of molecules.
引用
收藏
页码:2388 / 2393
页数:6
相关论文
共 41 条
[11]  
Gibson DG, 2009, NAT METHODS, V6, P343, DOI [10.1038/nmeth.1318, 10.1038/NMETH.1318]
[12]   REGULATION OF MALONYL-COA METABOLISM BY ACYL-ACYL CARRIER PROTEIN AND BETA-KETOACYL-ACYL CARRIER PROTEIN SYNTHASES IN ESCHERICHIA-COLI [J].
HEATH, RJ ;
ROCK, CO .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (26) :15531-15538
[13]   Engineering an Acinetobacter regulon for biosensing and high-throughput enzyme screening in E-coli via flow cytometry [J].
Jha, Ramesh K. ;
Kern, Theresa L. ;
Fox, David T. ;
Strauss, Charlie E. M. .
NUCLEIC ACIDS RESEARCH, 2014, 42 (12) :8150-8160
[14]   Recent advances in biological production of 3-hydroxypropionic acid [J].
Kumar, Vinod ;
Ashok, Somasundar ;
Park, Sunghoon .
BIOTECHNOLOGY ADVANCES, 2013, 31 (06) :945-961
[15]   A propionate-inducible expression system for enteric bacteria [J].
Lee, SK ;
Keasling, JD .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (11) :6856-6862
[16]   Catabolite repression of the propionate catabolic genes in Escherichia coli and Salmonella enterica:: Evidence for involvement of the cyclic AMP receptor protein [J].
Lee, SK ;
Newman, JD ;
Keasling, JD .
JOURNAL OF BACTERIOLOGY, 2005, 187 (08) :2793-2800
[17]   Independent and tight regulation of transcriptional units in Escherichia coli via the LacR/O, the TetR/O and AraC/I-1-I-2 regulatory elements [J].
Lutz, R ;
Bujard, H .
NUCLEIC ACIDS RESEARCH, 1997, 25 (06) :1203-1210
[18]   Expression of the sub-pathways of the Chloroflexus aurantiacus 3-hydroxypropionate carbon fixation bicycle in E. coli: Toward horizontal transfer of autotrophic growth [J].
Mattozzi, Matthew D. ;
Ziesack, Marika ;
Voges, Mathias J. ;
Silver, Pamela A. ;
Way, Jeffrey C. .
METABOLIC ENGINEERING, 2013, 16 :130-139
[19]   Use of modular, synthetic scaffolds for improved production of glucaric acid in engineered E. coli [J].
Moon, Tae Seok ;
Dueber, John E. ;
Shiue, Eric ;
Prather, Kristala L. Jones .
METABOLIC ENGINEERING, 2010, 12 (03) :298-305
[20]   Production of Glucaric Acid from a Synthetic Pathway in Recombinant Escherichia coli [J].
Moon, Tae Seok ;
Yoon, Sang-Hwal ;
Lanza, Amanda M. ;
Roy-Mayhew, Joseph D. ;
Prather, Kristala L. Jones .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2009, 75 (03) :589-595