Departamento de Alimentos e Nutrição Experimental, Faculdade de Ciências Farmacêuticas, Universidade de São Paulo, Avenida Professor Lineu Prestes, 580, Cidade Universitária, P. O. Box 05508-900, São Paulo, SP, Brazil.
J Ind Microbiol Biotechnol. 2010 Apr;37(4):381-90. doi: 10.1007/s10295-009-0684-y.
Bacteriocins produced by lactic acid bacteria are gaining increased importance due to their activity against undesirable microorganisms in foods. In this study, a concentrated acid extract of a culture of Lactobacillus sakei subsp. sakei 2a, a bacteriocinogenic strain isolated from a Brazilian pork product, was purified by cation exchange and reversed-phase chromatographic methods. The amino acid sequences of the active antimicrobial compounds determined by Edman degradation were compared to known protein sequences using the BLAST-P software. Three different antimicrobial compounds were obtained, P1, P2 and P3, and mass spectrometry indicated molecular masses of 4.4, 6.8 and 9.5 kDa, respectively. P1 corresponds to classical sakacin P, P2 is identical to the 30S ribosomal protein S21 of L. sakei subsp. sakei 23 K, and P3 is identical to a histone-like DNA-binding protein HV produced by L. sakei subsp. sakei 23 K. Total genomic DNA was extracted and used as target DNA for PCR amplification of the genes sak, lis and his involved in the synthesis of P1, P2 and P3. The fragments were cloned in pET28b expression vector and the resulting plasmids transformed in E. coli KRX competent cells. The transformants were active against Listeria monocytogenes, indicating that the activity of the classical sakacin P produced by L. sakei 2a can be complemented by other antimicrobial proteins.
由于其对食品中有害微生物的活性,乳酸菌产生的细菌素越来越受到重视。在这项研究中,从巴西猪肉制品中分离出的产细菌素的清酒乳杆菌亚种 2a 培养物的浓缩酸提取物通过阳离子交换和反相色谱方法进行了纯化。通过 Edman 降解确定的活性抗菌化合物的氨基酸序列与 BLAST-P 软件中的已知蛋白序列进行了比较。得到了三种不同的抗菌化合物,P1、P2 和 P3,质谱分析表明它们的分子量分别为 4.4、6.8 和 9.5 kDa。P1 对应于经典的 sakacin P,P2 与 L. sakei subsp. sakei 23 K 的 30S 核糖体蛋白 S21 相同,而 P3 与 L. sakei subsp. sakei 23 K 产生的组蛋白样 DNA 结合蛋白 HV 相同。提取总基因组 DNA 并用作合成 P1、P2 和 P3 的基因 sak、lis 和 his 的 PCR 扩增的靶 DNA。将片段克隆到 pET28b 表达载体中,并将得到的质粒转化到 E. coli KRX 感受态细胞中。转化体对单核细胞增生李斯特菌具有活性,表明 L. sakei 2a 产生的经典 sakacin P 的活性可以被其他抗菌蛋白补充。