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粘性放线菌对果聚糖的降解作用。

Degradation of levan by Actinomyces viscosus.

作者信息

Miller C H, Somers P J

出版信息

Infect Immun. 1978 Oct;22(1):266-74. doi: 10.1128/iai.22.1.266-274.1978.

DOI:10.1128/iai.22.1.266-274.1978
PMID:32137
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC422144/
Abstract

Actinomyces viscosus ATCC 15987 was examined for its ability to hydrolyze its own levan. Washed whole cells and an ammonium sulfate fraction from cell-free culture fluids were shown to possess levan hydrolase activity. Analyses of reaction mixtures by gel filtration and thin-layer chromatography demonstrated that the product of levan hydrolysis was free fructose. The cell-associated and extracellular enzyme preparations also hydrolyzed inulin and the levans synthesized by Aerobacter levanicum and Bacillus subtilis. Growth of A. viscosus in media supplemented with 0.1% A. viscosus levan resulted in a 33-fold increase and a 7-fold increase in the specific activities of the respective extracellular and cell-associated enzymes when compared with those from 55 mM glucose cultures. Growth in the presence of 29.2 mM sucrose resulted in a 28-fold increase and a 5-fold increase in the specific activities of the respective enzymes when compared with those from the glucose cultures. The extracellular enzyme exhibited high activity over a wide pH range, with 87 and 89% of its pH 6.0 optimum activity at pH 5.0 and 7.0, respectively. The cell-associated enzyme also exhibited optimum activity at pH 6.0, but this was decreased to 10 and 20% at pH 5.0 and 7.0, respectively. Analysis for the presence of extracellular levan during growth of A. viscosus in sucrose broths demonstrated that peak levan concentrations occurred during the mid-exponential to late-exponential phase of growth followed by a rapid decline in extracellular levan as a result of levan hydrolase activity.

摘要

对黏性放线菌ATCC 15987水解其自身果聚糖的能力进行了检测。结果表明,洗涤后的全细胞以及无细胞培养液的硫酸铵分级分离物具有果聚糖水解酶活性。通过凝胶过滤和薄层色谱对反应混合物进行分析,结果表明果聚糖水解产物为游离果糖。与细胞相关的酶制剂和细胞外酶制剂也能水解菊粉以及由产气杆菌和枯草芽孢杆菌合成的果聚糖。与在55 mM葡萄糖培养基中培养的黏性放线菌相比,在添加0.1%黏性放线菌果聚糖的培养基中生长时,相应的细胞外酶和与细胞相关的酶的比活性分别提高了33倍和7倍。在29.2 mM蔗糖存在的情况下生长时,与葡萄糖培养基中的相比,相应酶的比活性分别提高了28倍和5倍。细胞外酶在较宽的pH范围内表现出高活性,在pH 5.0和7.0时分别为其pH 6.0最佳活性的87%和89%。与细胞相关的酶在pH 6.0时也表现出最佳活性,但在pH 5.0和7.0时分别降至10%和20%。对黏性放线菌在蔗糖肉汤中生长期间细胞外果聚糖的存在情况进行分析表明,果聚糖浓度峰值出现在生长的指数中期至后期,随后由于果聚糖水解酶活性,细胞外果聚糖迅速下降。

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本文引用的文献

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