Recent achievements and perspectives for large-scale recombinant production of antimicrobial peptides

被引:63
|
作者
Wibowo, David [1 ,2 ]
Zhao, Chun-Xia [1 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
[2] Griffith Univ, Griffith Inst Drug Discovery, Nathan, Qld 4111, Australia
基金
澳大利亚研究理事会;
关键词
Antimicrobial peptides; Fusion proteins; Protein purification; Recombinant production; SOLUBLE PROKARYOTIC EXPRESSION; ESCHERICHIA-COLI; HETEROLOGOUS EXPRESSION; MOLECULAR-CLONING; BACILLUS-SUBTILIS; PROTEIN EXPRESSION; THIOREDOXIN-SUMO; AFFINITY TAGS; PURIFICATION; FUSION;
D O I
10.1007/s00253-018-9524-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Antibiotic resistance poses a growing threat to global public health. It is urgent to develop new alternative antibiotics. Antimicrobial peptide (AMP) is a diverse class of natural-occurring molecules that constitute immune systems of living organisms. More than 2500 AMPs have been identified and isolated from natural sources. Compared to conventional antibiotics, AMPs exhibit antimicrobial activities against a broad spectrum of microorganisms including bacteria, fungi, and even viruses. More importantly, the unique antimicrobial mechanisms of AMPs make it difficult for microorganisms to develop resistance. Therefore, it is very promising to develop AMPs as high-value antimicrobial candidates. This mini review provides an update of recent progresses in recombinant production of AMPs after fusion of AMP with carrier proteins and their scale-up. Key factors including selection of expression host and fusion tags are firstly introduced, followed by subsequent discussions on purification of fusion proteins and recovery of antimicrobial peptides. The scale production of AMPs is also explored.
引用
收藏
页码:659 / 671
页数:13
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