Reunanen J, Saris P E J
Applied Chemistry and Microbiology, University of Helsinki, FIN-00014 Helsinki, Finland.
Appl Environ Microbiol. 2003 Jul;69(7):4214-8. doi: 10.1128/AEM.69.7.4214-4218.2003.
A plasmid coding for the nisin two-component regulatory proteins, NisK and NisR, was constructed; in this plasmid a gfp gene (encoding the green fluorescent protein) was placed under control of the nisin-inducible nisF promoter. The plasmid was transformed into non-nisin-producing Lactococcus lactis strain MG1614. The new strain could sense extracellular nisin and transduce it to green fluorescent protein fluorescence. The amount of fluorescence was dependent on the nisin concentration, and it could be measured easily. By using this strain, an assay for quantification of nisin was developed. With this method it was possible to measure as little as 2.5 ng of pure nisin per ml in culture supernatant, 45 ng of nisin per ml in milk, 0.9 microg of nisin in cheese, and 1 microg of nisin per ml in salad dressings.
构建了一个编码乳链菌肽双组分调控蛋白NisK和NisR的质粒;在该质粒中,绿色荧光蛋白基因(gfp)置于乳链菌肽诱导型nisF启动子的控制之下。将该质粒转化到不产乳链菌肽的乳酸乳球菌MG1614菌株中。新菌株能够感知细胞外的乳链菌肽并将其转化为绿色荧光蛋白荧光。荧光量取决于乳链菌肽的浓度,且易于测量。利用该菌株开发了一种定量乳链菌肽的检测方法。通过这种方法,可以检测到培养上清液中低至每毫升2.5纳克的纯乳链菌肽、牛奶中每毫升45纳克的乳链菌肽、奶酪中0.9微克的乳链菌肽以及沙拉酱中每毫升1微克的乳链菌肽。