Stoakes L, Schieven B, Hussain Z, Lannigan R
Zentralbl Bakteriol Mikrobiol Hyg A. 1987 Apr;264(1-2):131-6. doi: 10.1016/s0176-6724(87)80132-3.
A carbohydrate degradation medium was developed for the detection of acid production by Neisseria species and Branhamella catarrhalis. A total of 223 clinical isolates were identified by Supplemented Peptone Agar and the results were compared with those of Cystine Trypticase Agar. Supplemented Peptone Agar and Cystine Trypticase Agar correctly identified 99.1% and 93.7% of the total strains respectively within 24 h. With Cystine Trypticase Agar method another 4% of the isolates could be identified but required an additional 24 h of incubation.
开发了一种碳水化合物降解培养基,用于检测奈瑟菌属和卡他布兰汉菌产酸情况。通过补充蛋白胨琼脂对总共223株临床分离株进行鉴定,并将结果与胱氨酸胰蛋白酶琼脂的鉴定结果进行比较。补充蛋白胨琼脂和胱氨酸胰蛋白酶琼脂分别在24小时内正确鉴定了99.1%和93.7%的总菌株。使用胱氨酸胰蛋白酶琼脂方法,另外4%的分离株可以被鉴定出来,但需要额外培养24小时。