Moats W A, Kinner J A
Appl Environ Microbiol. 1976 Mar;31(3):380-4. doi: 10.1128/aem.31.3.380-384.1976.
Several formulations of brilliant green agar with an added H2S indicator were evaluated. Results were optimum with variations of a basic formula consisting of 40 g of tryptic soy agar (Difco), 8 g of lactose, 8 g of sucrose, 80 mg of phenol red, 1 g of sulfanilamide, 1.5 g of ferric ammonium citrate, 5 g of sodium thiosulfate pentahydrate, and 7 mg of brilliant green dye per liter. Brilliant green dye was added after sterilization of the other components This formulation supported good growth of all of 39 strains of Salmonella tested. Normal biochemical types formed pink colonies with black centers, and an H2S-negative S. choleraesuis formed pink colonies without black centers. Of other bacteria tested, only Enterobacter, Klebsiella, and a few Citrobacter strains showed significant growth in 24 h. When lactose was omitted from the formulation, a lactose-fermenting strain formed pink colonies with black centers, and differentiation of Salmonella from the Enterobacter-Klebsiella groups was equally good. Addition of xylose (4.0 g) and L-lysine hydrochloride (5.4 g) to the above formulation improved differentiation between Salmonella and the few Citrobacter strains that grew and produced more intense blackening in Salmonella colonies. Addition of an H2S indicator to brilliant green agar formulations aided in identification of Salmonella colonies, especially in mixtures with other bacteria. These media were judged to give better differentiation of salmonellae from other bacteria than Hektoen agar with added novobiocin (10 mg/liter).
对几种添加了H2S指示剂的亮绿琼脂配方进行了评估。由每升40克胰蛋白胨大豆琼脂(Difco)、8克乳糖、8克蔗糖、80毫克酚红、1克磺胺、1.5克柠檬酸铁铵、5克五水硫代硫酸钠和7毫克亮绿染料组成的基本配方变体效果最佳。亮绿染料在其他成分灭菌后添加。该配方支持所测试的39株沙门氏菌全部良好生长。正常生化类型形成中心黑色的粉红色菌落,而H2S阴性的猪霍乱沙门氏菌形成无中心黑色的粉红色菌落。在其他测试细菌中,只有肠杆菌属、克雷伯氏菌属和少数柠檬酸杆菌属菌株在24小时内有显著生长。当配方中省略乳糖时,一株乳糖发酵菌株形成中心黑色的粉红色菌落,沙门氏菌与肠杆菌-克雷伯氏菌属菌群的鉴别同样良好。在上述配方中添加木糖(4.0克)和L-盐酸赖氨酸(5.4克)可改善沙门氏菌与少数生长的柠檬酸杆菌属菌株之间的鉴别,并使沙门氏菌菌落产生更强烈的变黑现象。向亮绿琼脂配方中添加H2S指示剂有助于沙门氏菌菌落的鉴定,尤其是在与其他细菌混合的情况下。与添加新霉素(10毫克/升)的赫克托恩琼脂相比,这些培养基被认为能更好地将沙门氏菌与其他细菌区分开来。