4.2 Article

Cell-free prototyping strategies for enhancing the sustainable production of polyhydroxyalkanoates bioplastics

期刊

SYNTHETIC BIOLOGY
卷 3, 期 1, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/synbio/ysy016

关键词

synthetic biology; cell-free transcription-translation; polyhydroxyalkanoates; biopolymers; whey permeate

资金

  1. Engineering and Physical Science Research Council (EPSRC) [EP/J02175X/1, EP/L011573/1]
  2. Biotechnology and Biological Sciences Research Council (BBSRC) Foundry grant [BB/L027852/1]
  3. BBSRC [BB/L027852/1, BB/M025632/1] Funding Source: UKRI
  4. EPSRC [EP/M006700/1, EP/L011573/1, EP/J02175X/1, EP/N023854/1] Funding Source: UKRI

向作者/读者索取更多资源

The polyhydroxyalkanoates (PHAs) are microbially-produced biopolymers that could potentially be used as sustainable alternatives to oil-derived plastics. However, PHAs are currently more expensive to produce than oil-derived plastics. Therefore, more efficient production processes would be desirable. Cell-free metabolic engineering strategies have already been used to optimize several biosynthetic pathways and we envisioned that cell-free strategies could be used for optimizing PHAs biosynthetic pathways. To this end, we developed several Escherichia coli cell-free systems for in vitro prototyping PHAs biosynthetic operons, and also for screening relevant metabolite recycling enzymes. Furthermore, we customized our cell-free reactions through the addition of whey permeate, an industrial waste that has been previously used to optimize in vivo PHAs production. We found that the inclusion of an optimal concentration of whey permeate enhanced relative cell-free GFPmut3b production by approximately 50%. In cell-free transcription-translation prototyping reactions, gas chromatography-mass spectrometry quantification of cell-free 3-hydroxybutyrate (3HB) production revealed differences between the activities of the Native Delta PhaC_C319A (1.18 +/- 0.39 mu M), C104 Delta PhaC_C319A (4.62 +/- 1.31 mu M) and C101 Delta PhaC_C319A (2.65 +/- 1.27 mu M) phaCAB operons that were tested. Interestingly, the most active operon, C104 produced higher levels of PHAs (or PHAs monomers) than the Native phaCAB operon in both in vitro and in vivo assays. Coupled cell-free biotransformation/transcription-translation reactions produced greater yields of 3HB (32.87 +/- 6.58 mu M), and these reactions were also used to characterize a Clostridium propionicum Acetyl-CoA recycling enzyme. Together, these data demonstrate that cell-free approaches complement in vivo workflows for identifying additional strategies for optimizing PHAs production.

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