Bouksaim M, Fliss I, Meghrous J, Simard R, Lacroix C
Centre de recherche en sciences et technologie du lait (STELA), Université Laval, Ste-Foy, Québec, Canada.
J Appl Microbiol. 1998 Feb;84(2):176-84. doi: 10.1046/j.1365-2672.1998.00315.x.
A highly specific antisera was produced in New Zealand white rabbits against nisin Z, a 3400 Da bacteriocin produced by Lactococcus lactis ssp. lactis biovar. diacetylactis UL 719. A dot immunoblot assay was then developed to detect nisin Z in milk and whey. As few as 1.5 10(-1) international units per ml (IU ml-1), corresponding to 0.003 microgram ml-1 of pure nisin Z, were detected in carbonate-bicarbonate buffer within 6 h using chemiluminescence. When milk and whey samples were tested, approximately 0.155 microgram ml-1 (7.9 IU ml-1) of nisin Z was detected. The detection limit obtained was lower than that of traditional methods including microtitration and agar diffusion.
针对乳酸乳球菌乳酸亚种双乙酰乳酸变种UL 719产生的3400 Da细菌素乳酸链球菌素Z,在新西兰白兔中制备了一种高度特异性的抗血清。然后开发了一种斑点免疫印迹法来检测牛奶和乳清中的乳酸链球菌素Z。使用化学发光法,在6小时内可在碳酸盐-碳酸氢盐缓冲液中检测到低至每毫升1.5×10⁻¹国际单位(IU ml⁻¹),相当于每毫升0.003微克纯乳酸链球菌素Z。当检测牛奶和乳清样品时,检测到约0.155微克/毫升(7.9 IU ml⁻¹)的乳酸链球菌素Z。获得的检测限低于包括微量滴定和琼脂扩散在内的传统方法。