| Literature DB >> 29366323 |
Jicong Cao1,2,3, Cesar de la Fuente-Nunez1,2,3, Rui Wen Ou4, Marcelo Der Torossian Torres1,2,5, Santosh G Pande6, Anthony J Sinskey4, Timothy K Lu1,2,3.
Abstract
Antibiotic resistance is one of the most challenging global health threats in our society. Antimicrobial peptides (AMPs) represent promising alternatives to conventional antibiotics for the treatment of drug-resistant infections. However, they are limited by their high manufacturing cost. Engineering living organisms represents a promising approach to produce such molecules in an inexpensive manner. Here, we genetically modified the yeast Pichia pastoris to produce the prototypical AMP apidaecin Ia using a fusion protein approach that leverages the beneficial properties ( e.g., stability) of human serum albumin. The peptide was successfully isolated from the fusion protein construct, purified, and demonstrated to have bioactivity against Escherichia coli. To demonstrate this approach as a manufacturing solution to AMPs, we scaled-up production in bioreactors to generate high AMP yields. We envision that this system could lead to improved AMP biomanufacturing platforms.Entities:
Keywords: Pichia pastoris; antimicrobials; protein production; synthetic biology; yeast
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Year: 2018 PMID: 29366323 DOI: 10.1021/acssynbio.7b00396
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110