Exploiting the Feedstock Flexibility of the Emergent Synthetic Biology Chassis Vibrio natriegens for Engineered Natural Product Production

被引:42
作者
Ellis, Gregory A. [1 ]
Tschirhart, Tanya [2 ]
Spangler, Joseph [3 ]
Walper, Scott A. [1 ]
Medintz, Igor L. [1 ]
Vora, Gary J. [1 ]
机构
[1] US Navy, Res Lab, Ctr Bio Mol Sci & Engn, Washington, DC 20375 USA
[2] US Navy, Res Lab, Amer Soc Engn Educ, Postdoctoral Res Associate, Washington, DC 20375 USA
[3] US Navy, Res Lab, Natl Acad Sci, Natl Res Council,Postdoctoral Res Associate, Washington, DC 20375 USA
基金
美国食品与农业研究所;
关键词
Vibrio; beta-carotene; violacein; marine bacteria; RECOMBINANT ESCHERICHIA-COLI; WHOLE MEVALONATE PATHWAY; BETA-CAROTENE; PSEUDOMONAS-NATRIEGENS; SUCROSE UTILIZATION; EXPRESSION; BIOSYNTHESIS; BACTERIUM; VIOLACEIN; BATCH;
D O I
10.3390/md17120679
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A recent goal of synthetic biology has been to identify new chassis that provide benefits lacking in model organisms. Vibrio natriegens is a marine Gram-negative bacterium which is an emergent synthetic biology chassis with inherent benefits: An extremely fast growth rate, genetic tractability, and the ability to grow on a variety of carbon sources ("feedstock flexibility"). Given these inherent benefits, we sought to determine its potential to heterologously produce natural products, and chose beta-carotene and violacein as test cases. For beta-carotene production, we expressed the beta-carotene biosynthetic pathway from the sister marine bacterium Vibrio campbellii, as well as the mevalonate biosynthetic pathway from the Gram-positive bacterium Lactobacillus acidophilus to improve precursor abundance. Violacein was produced by expressing a biosynthetic gene cluster derived from Chromobacterium violaceum. Not only was V. natriegens able to heterologously produce these compounds in rich media, illustrating its promise as a new chassis for small molecule drug production, but it also did so in minimal media using a variety of feedstocks. The ability for V. natriegens to produce natural products with multiple industrially-relevant feedstocks argues for continued investigations into the production of more complex natural products in this chassis.
引用
收藏
页数:21
相关论文
共 81 条
[1]   The Next Generation of Synthetic Biology Chassis: Moving Synthetic Biology from the Laboratory to the Field [J].
Adams, Bryn L. .
ACS SYNTHETIC BIOLOGY, 2016, 5 (12) :1328-1330
[2]   rRNA promoter activity in the fast-growing bacterium Vibrio natriegens [J].
Aiyar, SE ;
Gaal, T ;
Gourse, RL .
JOURNAL OF BACTERIOLOGY, 2002, 184 (05) :1349-1358
[3]   Metabolic engineering of Escherichia coli for limonene and perillyl alcohol production [J].
Alonso-Gutierrez, Jorge ;
Chan, Rossana ;
Batth, Tanveer S. ;
Adams, Paul D. ;
Keasling, Jay D. ;
Petzold, Christopher J. ;
Lee, Taek Soon .
METABOLIC ENGINEERING, 2013, 19 :33-41
[4]   Complete genome sequence of the probiotic lactic acid bacterium Lactobacillus acidophilus NCFM [J].
Altermann, E ;
Russell, WM ;
Azcarate-Peril, MA ;
Barrangou, R ;
Buck, BL ;
McAuliffe, O ;
Souther, N ;
Dobson, A ;
Duong, T ;
Callanan, M ;
Lick, S ;
Hamrick, A ;
Cano, R ;
Klaenhammer, TR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (11) :3906-3912
[5]  
[Anonymous], BIOSEPARATIONS SCI E
[6]  
[Anonymous], BIORXIV2016058487
[7]   Deletion of cscR in Escherichia coli W improves growth and poly-3-hydroxybutyrate (PHB) production from sucrose in fed batch culture [J].
Arifin, Yalun ;
Sabri, Suriana ;
Sugiarto, Haryadi ;
Kroemer, Jens O. ;
Vickers, Claudia E. ;
Nielsen, Lars K. .
JOURNAL OF BIOTECHNOLOGY, 2011, 156 (04) :275-278
[8]   In vitro biosynthesis of violacein from L-tryptophan by the enzymes VioA-E from Chromobacterium violaceum [J].
Balibar, Carl J. ;
Walsh, Christopher T. .
BIOCHEMISTRY, 2006, 45 (51) :15444-15457
[9]  
Benson DA, 2017, GenBank Nucleic Acids Res., V45, pD42
[10]   Phenotype MicroArrays for high-throughput phenotypic testing and assay of gene function [J].
Bochner, BR ;
Gadzinski, P ;
Panomitros, E .
GENOME RESEARCH, 2001, 11 (07) :1246-1255