A navigation guide of synthetic biology tools for Pseudomonas putida

被引:63
作者
Martin-Pascual, Maria [1 ]
Batianis, Christos [1 ]
Bruinsma, Lyon [1 ]
Asin-Garcia, Enrique [1 ]
Garcia-Morales, Luis [1 ]
Weusthuis, Ruud A. [2 ]
van Kranenburg, Richard [3 ,4 ]
dos Santos, Vitor A. P. Martins [1 ,5 ]
机构
[1] Wageningen Univ & Res, Lab Syst & Synthet Biol, NL-6708 WE Wageningen, Netherlands
[2] Wageningen Univ & Res, Bioproc Engn, Droevendaalsesteeg 1, NL-6708 PB Wageningen, Netherlands
[3] Corbion, NL-4206 AC Gorinchem, Netherlands
[4] Wageningen Univ & Res, Lab Microbiol, NL-6708 WE Wageningen, Netherlands
[5] LifeGlimmer GmbH, D-12163 Berlin, Germany
基金
荷兰研究理事会; 欧盟地平线“2020”;
关键词
Pseudomonas putida; Genetic toolbox; Genome editing; Synthetic biology; Chassis; Metabolic engineering; BROAD-HOST-RANGE; EUROPEAN VECTOR ARCHITECTURE; BACTERIAL GENE-EXPRESSION; SEQUENCE-SPECIFIC CONTROL; GRAM-NEGATIVE BACTERIA; SMALL RNA REGULATORS; P-COUMARIC ACID; ESCHERICHIA-COLI; ENGINEERING STRATEGIES; GENOME;
D O I
10.1016/j.biotechadv.2021.107732
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
Pseudomonas putida is a microbial chassis of huge potential for industrial and environmental biotechnology, owing to its remarkable metabolic versatility and ability to sustain difficult redox reactions and operational stresses, among other attractive characteristics. A wealth of genetic and in silico tools have been developed to enable the unravelling of its physiology and improvement of its performance. However, the rise of this microbe as a promising platform for biotechnological applications has resulted in diversification of tools and methods rather than standardization and convergence. As a consequence, multiple tools for the same purpose have been generated, whilst most of them have not been embraced by the scientific community, which has led to compartmentalization and inefficient use of resources. Inspired by this and by the substantial increase in popularity of P. putida, we aim herein to bring together and assess all currently available (wet and dry) synthetic biology tools specific for this microbe, focusing on the last 5 years. We provide information on the principles, functionality, advantages and limitations, with special focus on their use in metabolic engineering. Additionally, we compare the tool portfolio for P. putida with those for other bacterial chassis and discuss potential future directions for tool development. Therefore, this review is intended as a reference guide for experts and new 'users' of this promising chassis.
引用
收藏
页数:28
相关论文
共 275 条
[11]   A Multiplex Genome Editing Method for Escherichia coli Based on CRISPR-Cas12a [J].
Ao, Xiang ;
Yao, Yi ;
Li, Tian ;
Yang, Ting-Ting ;
Dong, Xu ;
Zheng, Ze-Tong ;
Chen, Guo-Qiang ;
Wu, Qiong ;
Guo, Yingying .
FRONTIERS IN MICROBIOLOGY, 2018, 9
[12]  
Aparicio T., 2015, HYDROCARBON LIPID MI
[13]   High-Efficiency Multi-site Genomic Editing of Pseudomonas putida through Thermoinducible ssDNA Recombineering [J].
Aparicio, Tomas ;
Nyerges, Akos ;
Martinez-Garcia, Esteban ;
de Lorenzo, Victor .
ISCIENCE, 2020, 23 (03)
[14]   Improved Thermotolerance of Genome-Reduced Pseudomonas putida EM42 Enables Effective Functioning of the PL/cI857 System [J].
Aparicio, Tomas ;
de Lorenzo, Victor ;
Martinez-Garcia, Esteban .
BIOTECHNOLOGY JOURNAL, 2019, 14 (01)
[15]   CRISPR/Cas9-Based Counterselection Boosts Recombineering Efficiency in Pseudomonas putida [J].
Aparicio, Tomas ;
de Lorenzo, Victor ;
Martinez-Garcia, Esteban .
BIOTECHNOLOGY JOURNAL, 2018, 13 (05)
[16]   The Ssr protein (T1E_1405) from Pseudomonas putida DOT-T1E enables oligonucleotide-based recombineering in platform strain P. putida EM42 [J].
Aparicio, Tomas ;
Jensen, Sheila I. ;
Nielsen, Alex T. ;
de Lorenzo, Victor ;
Martinez-Garcia, Esteban .
BIOTECHNOLOGY JOURNAL, 2016, 11 (10) :1309-1319
[17]   Tailor-made sRNAs: a plasmid tool to control the expression of target mRNAs in Pseudomonas putida [J].
Apura, Patricia ;
Saramago, Margarida ;
Peregrina, Alexandra ;
Viegas, Sandra C. ;
Carvalho, Sandra M. ;
Saraiva, Ligia M. ;
Arraiano, Cecilia M. ;
Domingues, Susana .
PLASMID, 2020, 109
[18]   Mutants IoxP vectors for selectable marker recycle and conditional knock-outs [J].
Arakawa H. ;
Lodygin D. ;
Buerstedde J.-M. .
BMC Biotechnology, 1 (1)
[19]   ACTIVITY OF THE HYBRID TRP-LAC(TAC) PROMOTER OF ESCHERICHIA-COLI IN PSEUDOMONAS-PUTIDA - CONSTRUCTION OF BROAD-HOST-RANGE, CONTROLLED-EXPRESSION VECTORS [J].
BAGDASARIAN, MM ;
AMANN, E ;
LURZ, R ;
RUCKERT, B ;
BAGDASARIAN, M .
GENE, 1983, 26 (2-3) :273-282
[20]   Genome-scale metabolic rewiring improves titers rates and yields of the non-native product indigoidine at scale [J].
Banerjee, Deepanwita ;
Eng, Thomas ;
Lau, Andrew K. ;
Sasaki, Yusuke ;
Wang, Brenda ;
Chen, Yan ;
Prahl, Jan-Philip ;
Singan, Vasanth R. ;
Herbert, Robin A. ;
Liu, Yuzhong ;
Tanjore, Deepti ;
Petzold, Christopher J. ;
Keasling, Jay D. ;
Mukhopadhyay, Aindrila .
NATURE COMMUNICATIONS, 2020, 11 (01)