生物制造
合成生物学
毕赤酵母
抗菌肽
酵母
大肠杆菌
抗菌剂
融合蛋白
肽
生物
抗生素
生物技术
生物制药
蛋白质工程
计算生物学
微生物学
重组DNA
生物化学
酶
基因
作者
Jicong Cao,César de la Fuente‐Núñez,Rui Wen Ou,Marcelo Der Torossian Torres,Santosh G. Pande,Anthony J. Sinskey,Timothy K. Lu
标识
DOI:10.1021/acssynbio.7b00396
摘要
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.
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