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用于检测厌氧菌产生明胶酶的明胶琼脂培养基。

Gelatin agar medium for detecting gelatinase production by anaerobic bacteria.

作者信息

Whaley D N, Dowell V R, Wanderlinder L M, Lombard G L

出版信息

J Clin Microbiol. 1982 Aug;16(2):224-9. doi: 10.1128/jcm.16.2.224-229.1982.

DOI:10.1128/jcm.16.2.224-229.1982
PMID:6288762
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC272334/
Abstract

A new medium, Lombard-Dowell gelatin agar, was developed for detecting gelatinase activity by anaerobic bacteria. The medium contained: Trypticase (BBL Microbiology Systems), 5.0 g; yeast extract (Difco Laboratories), 5 g; sodium chloride, 2.5 g; sodium sulfite, 0.1 g; L-tryptophan, 0.2 g; L-cystine, 0.4 g; hemin, 10.0 mg; vitamin K1, 10.0 mg; agar, 20.0 g; D-glucose, 1.0 g; gelatin, 4.0 g; and distilled water to 1 liter. The pH was adjusted to 7.5. The medium was dispensed in 100- by 15-mm quadrant plastic dishes (5 ml per quadrant). To test for gelatinase activity, we inoculated the medium with a young enriched thioglycolate or chopped meat glucose broth culture or a turbid cell suspension in Lombard-Dowell broth, using a sterile cotton swab, and incubated it under anaerobic conditions for 48 h at 35 degrees C. The quadrants were then flooded with Frazier solution, and clear zones around the bacterial growth were recorded as positive for gelatinase activity. The new medium was tested with a variety of anaerobic bacteria, and the results were compared with data obtained with the conventional technique for detecting gelatinase activity. Overall, there was satisfactory agreement between the two tests in the detection of gelatinase activity, but the Lombard-Dowell gelatin agar tests was more rapid and somewhat more sensitive than the conventional test.

摘要

一种新的培养基——伦巴德 - 道威尔明胶琼脂被开发出来用于检测厌氧菌的明胶酶活性。该培养基包含:胰蛋白酶(BBL微生物系统公司)5.0克;酵母提取物(Difco实验室)5克;氯化钠2.5克;亚硫酸钠0.1克;L - 色氨酸0.2克;L - 胱氨酸0.4克;血红素10.0毫克;维生素K1 10.0毫克;琼脂20.0克;D - 葡萄糖1.0克;明胶4.0克;加蒸馏水至1升。将pH值调至7.5。将培养基分装到100×15毫米的四象限塑料培养皿中(每象限5毫升)。为检测明胶酶活性,我们用无菌棉拭子蘸取年轻的硫乙醇酸盐或碎肉葡萄糖肉汤富集培养物或伦巴德 - 道威尔肉汤中的浑浊细胞悬液接种该培养基,并在35℃厌氧条件下培养48小时。然后在各象限加入弗雷泽溶液,细菌生长周围出现的透明圈记录为明胶酶活性阳性。用多种厌氧菌对这种新培养基进行了测试,并将结果与用传统技术检测明胶酶活性所获得的数据进行了比较。总体而言,在检测明胶酶活性方面,两种测试结果之间的一致性令人满意,但伦巴德 - 道威尔明胶琼脂测试比传统测试更快速,且灵敏度略高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38d1/272334/bd9d01ea071a/jcm00145-0041-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38d1/272334/bd9d01ea071a/jcm00145-0041-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38d1/272334/bd9d01ea071a/jcm00145-0041-a.jpg

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