4.7 Article

Production of PHA copolymers consisting of 3-hydroxybutyrate and 3-hydroxyhexanoate (PHBHHx) by recombinant Halomonas bluephagenesis

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 466, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2023.143261

Keywords

PHBHHx; Expression-tuning; beta-oxidation; Chromosome engineering; Halomonas; Next generation industrial biotechnology

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This study aims to produce low-cost poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBHHx) with customized and/or rich 3HHx by engineering Halomonas bluephagenesis. Through the expression of heterologous PHA synthase (PhaC(ac)) and enoyl coenzyme-A hydratase (PhaJ(ac)), PHBHHx with high 3HHx ratios was obtained. Furthermore, by weakening the native beta-oxidation pathway, PHBHHx with up to 49 mol% 3HHx was synthesized.
Microbial synthesized poly(3-hydroxybutyrate-co-3-hydroxyhexanoate), namely PHBHHx, with different 3HHx monomer ratios have shown biocompatibility, biodegradability and flexibility for commercial uses. This study aims at the low-cost production of PHBHHx with customized and/or rich 3HHx by engineered Halomonas bluephagenesis (H. bluephagenesis), which is a rising-star chassis for Next Generation Industrial Biotechnology (NGIB). Recombinant H. bluephagenesis harboring heterologous PHA synthase (PhaC(ac)) and enoyl coenzyme-A hydratase (PhaJ(ac)) could produce PHBHHx from glucose and sodium hexanoate. After rationally fine-tuning the expression levels of phaC(ac) and phaJ(ac) employing two inducible promoters, P-lac and P-lux induced by IPTG and AHL, respectively, the resulting H. bluephagenesis TDC-CJ produced 55 wt% P(3HB-co-14.21 mol% 3HHx). Furthermore, two inducible promoters were replaced by constitutive ones, P-porin68 and P-porin58, respectively, with similar expression strength to remove the additions of inducers. Notably, PHBHHx of high 3HHx ratios, reaching up to 49 mol%, was further obtained by weakening the native beta-oxidation pathway. Finally, chromosomally engineered H. bluephagenesis G34 with two expression cassettes of phaCJ on loci G3 and G4 was constructed to achieve the synthesis of P(3HB-co-36 mol% 3HHx) without supplementing antibiotic. For lab-scale fermentation in a 7-L bioreactor, H. bluephagenesis G34 produced PHBHHx with controllable molar fraction of 3HHx from 0-to-37 mol% by designing glucose/hexanoate ratio. These efforts demonstrate that engineering H. bluephagenesis is of great potential for PHBHHx production of low cost for industrial-scale biomanufacturing purpose.

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