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Production of protein-based polymers in Pichia pastoris
Authors:Marc WT Werten  Gerrit Eggink  Martien A Cohen Stuart  Frits A de Wolf
Institution:1. Wageningen Food & Biobased Research, NL-6708 WG Wageningen, The Netherlands;2. Bioprocess Engineering, Wageningen University & Research, NL-6708 PB Wageningen, The Netherlands;3. Physical Chemistry and Soft Matter, Wageningen University & Research, NL-6708 WE Wageningen, The Netherlands
Abstract:Materials science and genetic engineering have joined forces over the last three decades in the development of so-called protein-based polymers. These are proteins, typically with repetitive amino acid sequences, that have such physical properties that they can be used as functional materials. Well-known natural examples are collagen, silk, and elastin, but also artificial sequences have been devised. These proteins can be produced in a suitable host via recombinant DNA technology, and it is this inherent control over monomer sequence and molecular size that renders this class of polymers of particular interest to the fields of nanomaterials and biomedical research. Traditionally, Escherichia coli has been the main workhorse for the production of these polymers, but the methylotrophic yeast Pichia pastoris is finding increased use in view of the often high yields and potential bioprocessing benefits. We here provide an overview of protein-based polymers produced in P. pastoris. We summarize their physicochemical properties, briefly note possible applications, and detail their biosynthesis. Some challenges that may be faced when using P. pastoris for polymer production are identified: (i) low yields and poor process control in shake flask cultures; i.e., the need for bioreactors, (ii) proteolytic degradation, and (iii) self-assembly in vivo. Strategies to overcome these challenges are discussed, which we anticipate will be of interest also to readers involved in protein expression in P. pastoris in general.
Keywords:Corresponding author at: Wageningen Food & Biobased Research  NL-6708 WG Wageningen  The Netherlands    Protein-based polymers  Protein expression  Proteolysis  Silk  Collagen  Gelatin  Elastin  Block copolymers  Self-assembly  alcohol oxidase 1  BiP  immunoglobulin-binding protein  DPAPase A  dipeptidyl aminopeptidase A  EBP  elastin-binding protein  ECM  extracellular matrix  ELP  elastin-like polypeptide  ERAD  ER-associated degradation  FDA  food and drug administration  glyceraldehyde-3-phosphate dehydrogenase  GRAS  generally recognized as safe  histidinol dehydrogenase  ITC  inverse transition cycling  LCST  lower critical solution temperature  MaSp1  major ampullate spidroin 1  MaSp2  major ampullate spidroin 2  600  optical density at 600 nm  P4H  peptidyl-prolyl-4-hydroxylase  PDI  protein disulfide isomerase  Pho1  acid phosphatase  ppαF  UPR  unfolded protein response
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