| Literature DB >> 31546303 |
Hyeok-Won Lee1, Jung-Ho Park2, Hee-Seok Lee1,3, Wonho Choi2, Sung-Hwa Seo1, Irika Devi Anggraini1,3, Eui-Sung Choi1,3, Hong-Weon Lee1,3.
Abstract
Isoprene has the potential to replace some petroleum-based chemicals and can be produced through biological systems using renewable carbon sources. Ralstonia eutropha can produce value-added compounds, including intracellular polyhydroxyalkanoate (PHA) through fatty acid and lipid metabolism. In the present study, we engineered strains of R. eutropha H16 and examined the strains for isoprene production. We optimized codons of all the genes involved in isoprene synthesis by the mevalonate pathway and manipulated the promoter regions using pLac and pJ5 elements. Our results showed that isoprene productivity was higher using the J5 promoter (1.9 ± 0.24 µg/l) than when using the lac promoter (1.5 ± 0.2 µg/l). Additionally, the use of three J5 promoters was more efficient (3.8 ± 0.18 µg/l) for isoprene production than a one-promoter system, and could be scaled up to a 5-L batch-cultivation from a T-flask culture. Although the isoprene yield obtained in our study was insufficient to meet industrial demands, our study, for the first time, shows that R. eutropha can be modified for efficient isoprene production and lays the foundation for further optimization of the fermentation process.Entities:
Keywords: MVA pathway; Ralstonia eutropha; fermentation; isoprene production; promoter
Year: 2019 PMID: 31546303 DOI: 10.4014/jmb.1909.09002
Source DB: PubMed Journal: J Microbiol Biotechnol ISSN: 1017-7825 Impact factor: 2.351