High expression of a plectasin-derived peptide NZ2114 in Pichia pastoris and its pharmacodynamics, postantibiotic and synergy against Staphylococcus aureus

被引:102
作者
Zhang, Yong [1 ,2 ]
Teng, Da [1 ,2 ]
Mao, Ruoyu [1 ,2 ]
Wang, Xiumin [1 ,2 ]
Xi, Di [1 ,2 ]
Hu, Xiaoyuan [1 ,2 ]
Wang, Jianhua [1 ,2 ]
机构
[1] Minist Agr, Key Lab Feed Biotechnol, Beijing 100081, Peoples R China
[2] Chinese Acad Agr Sci, Feed Res Inst, Gene Engn Lab, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
NZ2114; Pichia pastoris; MRSA; PAE; Synergy; ANTIMICROBIAL PEPTIDES; UNITED-STATES; HETEROLOGOUS EXPRESSION; RECOMBINANT EXPRESSION; ESCHERICHIA-COLI; INFECTIONS; VANCOMYCIN; PROTEIN; RESISTANCE; STRATEGIES;
D O I
10.1007/s00253-013-4881-2
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
NZ2114, a new variant of plectasin, was overexpressed in Pichia pastoris X-33 via pPICZ alpha A for the first time. The total secreted protein of fermentation supernatant reached 2,390 mg/l (29 A degrees C) and 2,310 mg/l (25 A degrees C), and the recombinant NZ2114 (rNZ2114) reached 860 mg/l (29 A degrees C) and 1,309 mg/l (25 A degrees C) at 96 h induction in a 5-l fermentor, respectively.The rNZ2114 was purified by cation exchange chromatography, and its yield was 583 mg/l with 94.8 % purity. The minimal inhibitory concentration (MIC) of rNZ2114 to four ATCC strains of Staphyloccocus aureus was evaluated from 0.028 to 0.90 mu M. Meanwhile, it showed potent activity (0.11-0.90 mu M) to 20 clinical isolates of MRSA. The rNZ2114 killed over 99.9 % of tested S. aureus (ATCC 25923 and ATCC 43300) in Mueller-Hinton medium within 6 h when treated with 4 x MIC. The postantibiotic effect of rNZ2114 to S. aureus ATCC 25923 and ATCC 43300 was 18.6-45.6 and 1.7-3.5 h under 1x, 2x, and 4x MIC, respectively. The fractional inhibitory concentration index (FICI) indicated a synergistic effect between rNZ2114 and kanamycin, streptomycin, and vancomycin against S. aureus ATCC 25923 (FICI = 0.125), and additivity between rNZ2114 and ampicillin, spectinomycin (FICI = 0.625), respectively. To S. aureus ATCC 43300 [methicillin-resistant S. aureus (MRSA)], rNZ2114 showed a synergistic effect (FICI = 0.125-0.3125) with kanamycin, ampicillin, streptomycin, and vancomycin, and antagonism with spectinomycin (FICI = 8.0625). The rNZ2114 caused only less than 0.1 % hemolytic activity in the concentration of 128 mu g/ml, and showed a good thermostability from 20 to 80 A degrees C. In addition, it exhibited the highest activity at pH 8.0. These results suggested that large-scale production of NZ2114 is feasible using the P. pastoris expression system, and it could be a new potential antimicrobial agent for the prevention and treatment of S. aureus especially for MRSA infections.
引用
收藏
页码:681 / 694
页数:14
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