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 D. T. 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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