High production of poly-β-hydroxybutyrate (PHB) by an Azotobacter vinelandii mutant altered in PHB regulation using a fed-batch fermentation process

被引:64
作者
Garcia, A. [1 ]
Segura, D. [2 ]
Espin, G. [2 ]
Galindo, E. [1 ]
Castillo, T. [1 ]
Pena, C. [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Ingn Celular & Biocatalisis, Cuernavaca 62250, Morelos, Mexico
[2] Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Mol Microbiol, Cuernavaca 62250, Morelos, Mexico
关键词
Poly-beta-hydroxybutyrate; Azotobacter vinelandii; Fed-batch cultures; Mutant; Fermentation; Dissolved oxygen; ALGINATE BIOSYNTHESIS; ALCALIGENES-EUTROPHUS; PHOSPHATE LIMITATION; MOLECULAR-MASS; CULTURE; POLY(3-HYDROXYBUTYRATE); GROWTH; GENES; POLYHYDROXYBUTYRATE; OXYGEN;
D O I
10.1016/j.bej.2013.10.020
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
A mixed fermentation strategy based on exponentially fed-batch cultures (EFBC) and nutrient pulses with sucrose and yeast extract was developed to achieve a high concentration of PHB by Azotobacter vinelandii OPNA, which carries a mutation on the regulatory systems PTSNtr and RsmA-RsmZ/Y, that negatively regulate the synthesis of PHB. Culture of the OPNA strain in shake Oaks containing PY-sucrose medium significantly improved growth and PHB production with respect to the results obtained from the cultures with the parental strain (OP). When the OPNA strain was cultured in a batch fermentation keeping constant the DOT at 4%, the maximal growth rate (0.16 h(-1)) and PHB yield (0.30 g(PHB) g(Suc)(-1)) were reached. Later, in EFBC, the OPNA strain increased three fold the biomass and 2.2 fold the PHB concentration in relation to the values obtained from the batch cultures. Finally, using a strategy of exponential feeding coupled with nutrient pulses (with sucrose and yeast extract) the production of PHB increased 7-fold to reach a maximal PHB concentration of 27.3 +/- 3.2 g L-1 at 60 h of fermentation. Overall, the use of the mutant of A. vinelandii OPNA, impaired in the PHB regulatory systems, in combination with a mixed fermentation strategy could be a feasible strategy to optimize the PHB production at industrial level. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:117 / 123
页数:7
相关论文
共 45 条
[1]   Process design for microbial plastic factories: metabolic engineering of polyhydroxyalkanoates [J].
Aldor, AS ;
Keasling, JD .
CURRENT OPINION IN BIOTECHNOLOGY, 2003, 14 (05) :475-483
[2]   POLYMER SYNTHESIS BY MICROORGANISMS - TECHNOLOGY AND ECONOMICS [J].
BYROM, D .
TRENDS IN BIOTECHNOLOGY, 1987, 5 (09) :246-250
[3]   The GacS sensor kinase regulates alginate and poly-β-hydroxybutyrate production in Azotobacter vinelandii [J].
Castañeda, M ;
Guzmán, J ;
Moreno, S ;
Espín, G .
JOURNAL OF BACTERIOLOGY, 2000, 182 (09) :2624-2628
[4]  
Castillo M.T., 2013, J IND MICROBIOL BIOT, DOI DOI 10.1007/S10295-013-1274-6
[5]   Production of poly-beta-hydroxybutyrate by Azotobacter vinelandii in a two-stage fermentation process [J].
Chen, GQ ;
Page, WJ .
BIOTECHNOLOGY TECHNIQUES, 1997, 11 (05) :347-350
[6]   Factors affecting the economics of polyhydroxyalkanoate production by bacterial fermentation [J].
Choi, J ;
Lee, SY .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1999, 51 (01) :13-21
[7]   The oxygen transfer rate influences the molecular mass of the alginate produced by Azotobacter vinelandii [J].
Diaz-Barrera, A. ;
Pena, C. ;
Galindo, E. .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2007, 76 (04) :903-910
[8]  
Flores C., 2013, ENZYME MICROB TECHNO, DOI DOI 10.1016/J.ENZMICTEC.04.010
[9]   Molecular and bioengineering strategies to improve alginate and polydydroxyalkanoate production by Azotobacter vinelandii [J].
Galindo, Enrique ;
Pena, Carlos ;
Nunez, Cinthia ;
Segura, Daniel ;
Espin, Guadalupe .
MICROBIAL CELL FACTORIES, 2007, 6 (1)
[10]   Bacterial Polyhydroxyalkanoate Granules: Biogenesis, Structure, and Potential Use as Nano-/Micro-Beads in Biotechnological and Biomedical Applications [J].
Grage, Katrin ;
Jahns, Anika C. ;
Parlane, Natalie ;
Palanisamy, Rajasekaran ;
Rasiah, Indira A. ;
Atwood, Jane A. ;
Rehm, Bernd H. A. .
BIOMACROMOLECULES, 2009, 10 (04) :660-669