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利用荧光底物分析空气中的放线菌孢子。

Analysis of airborne actinomycete spores with fluorogenic substrates.

作者信息

Gazenko S V, Reponen T A, Grinshpun S A, Willeke K

机构信息

Aerosol Research and Exposure Assessment Laboratory, Department of Environmental Health, University of Cincinnati, Cincinnati, Ohio 45267-0056, USA.

出版信息

Appl Environ Microbiol. 1998 Nov;64(11):4410-5. doi: 10.1128/AEM.64.11.4410-4415.1998.

Abstract

The reactions between seven fluorogenic substrates and different groups of enzymes, esterases, lipases, phosphatases, and dehydrogenases, were studied in a search for a new method for the detection of actinomycete spores. Fluorescence measurement was chosen as a fast and sensitive method for microbial analysis. The focus of the research was on the spores of important air contaminants: Streptomyces albus and Thermoactinomyces vulgaris. For the measurement of the enzymatic activity, the chosen fluorogenic substrate was added to a mixture of spores and nutrient media, and the resulting fluorescence was measured with a spectrofluorometer. Fluorogenic substrates were found to show enzymatic activities even for dormant spores. Comparison of the enzymatic activities of dormant spores with those of vegetative cells showed similarity of the enzymatic profiles but higher activity for vegetative cells. The increase of enzymatic activity from dormant spores to vegetative cells was not linear but fluctuating. The largest fluctuations were found after 4 to 5 h of incubation. The enzymatic activities of S. albus were 10 to 50 times lower than those of T. vulgaris, except for the dehydrogenase activity, which was seven times higher. These results indicate that analysis with fluorogenic substrates has the potential for becoming a fast and sensitive method for the enumeration and identification of airborne actinomycete spores.

摘要

研究了七种荧光底物与不同种类酶(酯酶、脂肪酶、磷酸酶和脱氢酶)之间的反应,以寻找一种检测放线菌孢子的新方法。荧光测量被选为一种快速且灵敏的微生物分析方法。该研究的重点是重要空气污染物的孢子:白色链霉菌和普通嗜热放线菌。为了测量酶活性,将选定的荧光底物添加到孢子和营养培养基的混合物中,并用荧光分光光度计测量产生的荧光。发现荧光底物即使对休眠孢子也显示出酶活性。将休眠孢子的酶活性与营养细胞的酶活性进行比较,结果表明酶谱相似,但营养细胞的活性更高。从休眠孢子到营养细胞,酶活性的增加不是线性的,而是波动的。在培养4至5小时后发现波动最大。除脱氢酶活性高7倍外,白色链霉菌的酶活性比普通嗜热放线菌低10至50倍。这些结果表明,用荧光底物进行分析有潜力成为一种快速且灵敏的方法,用于对空气中放线菌孢子进行计数和鉴定。

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