Efficient production of (R)-3-hydroxybutyric acid by Pseudomonas sp. DS1001a and its extracellular poly(3-hydroxybutyrate) depolymerase. Issue 3 (March 2016)

• Record Type: Journal Article
• Authors: Li, Fan; Zhang, Chunyu; Liu, Yuting; Liu, Dongbo; Xia, Hongmei; Chen, Shan
• Is Part Of: Process biochemistry. Volume 51:Issue 3(2016:Mar.)
• Page Start: 369
• Page End: 373
• Publication Date: 2016-03
• Subjects: (R)-3-Hydroxybutyric acid -- Pseudomonas sp. DS1001a -- PHB depolymerase -- Bioconversion; Biochemical engineering -- Periodicals; Biotechnology -- Periodicals; Biochemistry -- periodicals; Biotechnology -- periodicals; Chemical Engineering -- periodicals; Génie biochimique -- Périodiques; Biotechnologie -- Périodiques; Biochemical engineering; Biotechnology; Periodicals; 660.63
• DOI: 10.1016/j.procbio.2015.12.016
• Languages: English
• ISSNs: 1359-5113

Abstract

Graphical abstract: We demonstrated a novel strategy to produce (R)-3-hydroxybutyric acid [(R)-3-HB] by microorganism or depolymerase in vivo. MS and HPLC assay of PHB hydrolysis product by Pseudomonas sp. DS1001a and its PHB depolymerase were carried out. The results show that (R)-3-HB monomer with a peak at m / z 103, rather than the dimer, trimer, or other oligomers, was detected in the water-soluble products (a and c). The HPLC chromatograms of the monomer product and (R)-3-HB standard matched perfectly (b and d). Yields of 0.130 g/l h and 1.073 g/l h were achieved by strain and crude enzyme, respectively. CaCO3 added in depolymerase increased (R)-3-HB yields efficiently; suggesting the bioconversions from low-valued PHB wastes or industrial leftovers to high-valued (R)-3-HB using extracellular PHB depolymerase is attractive. Highlights: An alternative strategy for production of ( R )-3-hydroxybutyric acid was demonstrated. The strategy involved bioconversion by Pseudomonas sp. and its extracellular depolymerase. Yields of 0.130 g/l h and 1.073 g/l h were achieved by strain and crude enzyme, respectively. CaCO3 increased yields to 3 g/l h by stabilizing the pH of the reaction system. Abstract: We demonstrate a novel strategy to produce ( R )-3-hydroxybutyric acid [( R )-3-HB] using Pseudomonas sp. DS1001a or its extracellular poly (3-hydroxybutyrate) (PHB) depolymerase. While approximately 77.8% PHB was degraded by Pseudomonas sp. DS1001a after 12 h of cultivation, only 1.555 g/l of 3-HB monomer was produced because of assimilation by the strain. About 8.58 g/l ( R )-3-HB was obtained after 8 h of incubation using extracellular PHB depolymerase from Pseudomonas sp. DS1001a. The optimal temperature and pH of PHB depolymerase were 50 °C and 8, respectively. CaCO3 increased ( R )-3-HB yields to 23.97 g/l by stabilizing the pH of the reaction system. High yields of the ( R )-3-HB product and the low cost of the medium and CaCO3 indicate the feasibility of bioconversion of low-value PHB waste or industrial leftovers into high-value ( R )-3-HB using extracellular PHB depolymerase.