4.5 Review

Improving biological production of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) co-polymer: a critical review

Journal

Publisher

SPRINGER
DOI: 10.1007/s11157-021-09575-z

Keywords

3HV precursors; Biorefinery; Metabolic engineered microorganisms; High performance biomaterials; PHBV

Funding

  1. Universita` degli Studi di Napoli Federico II within the CRUI-CARE Agreement

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This study compares methods to enhance the yield of PHBV copolymer biologically produced and reduce costs, including the addition of 3HV precursors to increase the hydroxyvalerate fraction, the use of wild bacterial species to produce hydroxyvalerate from unrelated carbon sources, and the use of metabolic engineering techniques to promote independent biosynthesis pathways. The selection of suitable substrate-microorganism combinations is crucial for process optimization.
Although poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) is the most promising biopolymer for petroleum-based plastics replacement, the low processes productivity as well as the high sale price represent a major barrier for its widespread usage. The present work examines comparatively the existing methods to enhance the yield of the PHBV copolymer biologically produced and/or reduce their costs. The study is addressed to researchers working on the development of new biological production methods and/or the improvement of those currently used. At this aim, the authors have considered the analysis of some crucial aspects related to substrates and microorganism's choice. The production strategies have been individuated, presented and discussed, either based on a single aspect (type of substrate or microorganism) or based on combined aspects (type of substrate and microorganism). Process operating conditions have been discussed as well. The analysis indicates that the addition of 3HV precursors is capable to dramatically enhance the hydroxyvalerate fraction in the produced biopolymers. On the other hand, due to the high costs of the 3HV precursors, the utilization of wild bacterial species capable to produce the hydroxyvalerate fraction from unrelated carbon sources (i.e. no 3HV precursors) also can be considered a valuable strategy for costs reduction. Moreover, metabolic engineering techniques can be successfully used to promote 3HV precursors-independent biosynthesis pathways and enhance the process productivity. The use of mixed cultures or extremophile bacteria avoids the need of sterile working conditions, and therefore favours the process scale-up. The utilization of the organic waste as substrate plays a key role for a sharp reduction of production costs. Finally, the selection of the most suitable substrate-microorganism combination cannot be separated by the adoption of an appropriate choice of reactor configuration and abiotic factors.

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