Engineering of Halomonas bluephagenesis for low cost production of poly(3-hydroxybutyrate-co-4-hydroxybutyrate) from glucose
Poly(3-hydroxybutyrate-co−4-hydroxybutyrate) [P(3HB-co−4HB)] is one of the most promising biomaterials expected to be used in a wide range of scenarios. However, its large-scale production is still hindered by the high cost. Here we report the engineering of Halomonas bluephagenesis as a low-cost pl...
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Veröffentlicht in: | Metabolic engineering 2018-05, Vol.47, p.143-152 |
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Sprache: | eng |
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Zusammenfassung: | Poly(3-hydroxybutyrate-co−4-hydroxybutyrate) [P(3HB-co−4HB)] is one of the most promising biomaterials expected to be used in a wide range of scenarios. However, its large-scale production is still hindered by the high cost. Here we report the engineering of Halomonas bluephagenesis as a low-cost platform for non-sterile and continuous fermentative production of P(3HB-co−4HB) from glucose. Two interrelated 4-hydroxybutyrate (4HB) biosynthesis pathways were constructed to guarantee 4HB monomer supply for P(3HB-co−4HB) synthesis by working in concert with 3-hydroxybutyrate (3HB) pathway. Interestingly, only 0.17 mol% 4HB in the copolymer was obtained during shake flask studies. Pathway debugging using structurally related carbon source located the failure as insufficient 4HB accumulation. Further whole genome sequencing and comparative genomic analysis identified multiple orthologs of succinate semialdehyde dehydrogenase (gabD) that may compete with 4HB synthesis flux in H. bluephagenesis. Accordingly, combinatory gene-knockout strains were constructed and characterized, through which the molar fraction of 4HB was increased by 24-fold in shake flask studies. The best-performing strain was grown on glucose as the single carbon source for 60 h under non-sterile conditions in a 7-L bioreactor, reaching 26.3 g/L of dry cell mass containing 60.5% P(3HB-co−17.04 mol%4HB). Besides, 4HB molar fraction in the copolymer can be tuned from 13 mol% to 25 mol% by controlling the residual glucose concentration in the cultures. This is the first study to achieve the production of P(3HB-co−4HB) from only glucose using Halomonas.
•Halomonas bluephagenesis was engineered to produce P(3HB-co−4HB) from glucose in non-sterile fermentation.•Comparative genome analysis were used for pathway debugging and significantly improved P(3HB-co−4HB) synthesis.•P(3HB-co−25 mol% 4HB) was produced by engineered H. bluephagenesis utilizing glucose only.•Next-generation industrial biotechnology was successfully applied to P(3HB-co−4HB) production. |
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ISSN: | 1096-7176 1096-7184 |
DOI: | 10.1016/j.ymben.2018.03.013 |