黑海分离细菌角化酶、干酪子酶、纤维素酶和β-甘露聚糖酶活性的研究

Q4 Biochemistry, Genetics and Molecular Biology
O. Gudzenko, K. V. Avdiyuk, N. Borzova, V. Ivanytsia, L. Varbanets
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引用次数: 1

摘要

长期以来,对海洋环境的主要兴趣,被认为是极端的,是分离和鉴定具有生物特性的天然产物,为此,对许多生物和化学结构进行了研究。因此,从各种底物中分离出来的海洋细菌,如沉积物、海水和红树林碎屑,是具有不同活性的酶的产生者,即淀粉酶、纤维素酶、海藻酸解酶、几丁质酶、葡萄糖苷酶、菊糖酶、角化酶、木质素酶、木聚糖酶等。如今,研究人员也在关注海洋环境中产生的具有特殊性质的酶。因此,本研究的目的是研究海洋微生物菌株表现出纤维素酶、β-甘露聚糖酶、角化酶和酪蛋白溶酶活性的能力。方法。研究了培养液上清液的酶活性。分别以瓜尔胶半乳甘露聚糖和na -羧甲基纤维素为底物测定β-甘露聚糖酶和纤维素酶活性。酪蛋白和去脂碎羽毛作为底物测定蛋白水解活性。结果。在含有鸡毛作为碳氮唯一来源的营养培养基(营养培养基1)上培养10个微生物没有产生阳性结果。使用培养基2时,4株菌株(51、52、54、247)在培养液(CLS)上清液中均有活性生长,对角蛋白(6.0 ~ 16.0 U/mL)和酪蛋白(0.025 ~ 0.33 U/mL)均有活性。在研究的10个培养物中,只有6个(7、20、51、52、50、247)的CLS中观察到纤维素酶和β-甘露聚糖酶的活性。培养物20的纤维素酶活性最高(1.8 U/mL)。培养7活性稍低,为1.0 U/mL。在培养物54 (0.06 U/mL)、56和50 (0.05 U/mL)中,活性不显著。在培养247中观察到微量的活性水平。结论。菌株7、20、247和51是首次从黑海分离到的菌株,作为纤维素酶、β-甘露聚糖酶、角化酶和酪蛋白溶酶的产生物,具有进一步研究的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Keratinase, Caseinolitic, Cellulase and β-Mananase Activities of Bacteria Isolated from the Black Sea
For a long time, the main interest in the marine environment, considered extreme, was the isolation and identification of natural products with biological properties, and for that, numerous organisms and chemical structures have been studied. Thus, marine bacteria isolated from various substrates, such as sediments, seawater, and mangrove detritus, are producers of enzymes with different activities, i.e., amylase, cellulase, alginate lyase, chitinase, glucosidase, inulinase, keratinase, ligninase, xylanase, and others. Nowadays, researchers are also focusing on the enzymes produced in the marine environment that can present special properties. Therefore, the aim of this study was to investigate the ability of marine strains of microorganisms to exhibit cellulase, β-mannanase, keratinase, and caseinolytic activities. Methods. Enzymatic activities were studied in the culture liquid supernatant. To determine β-mannanase and cellulase activities, guar gum galactomannan and Na-carboxymethylcellulose respectively were used as substrates. Casein and crushed defatted feathers served as substrates for the determination of proteolytic activity. Results. Growing 10 cultures of microorganisms on a nutrient medium containing chicken feathers as the sole source of carbon and nitrogen (nutrient medium 1) did not give positive results. When using medium 2, active growth was observed in four of the studied strains (51, 52, 54, 247) in the supernatant of culture liquid (CLS), the activity of which both to keratin (6.0—16.0 U/mL) and casein (0.025—0.33 U/mL) was found. In the CLS of only six of the 10 studied cultures (7, 20, 51, 52, 50, 247), cellulase and β-mannanase activities were observed. The highest cellulase activity was found in culture 20 (1.8 U/mL). The activity of culture 7 was somewhat lower (1.0 U/mL). An insignificant activity was noted in cultures 54 (0.06 U/mL), 56, and 50 (0.05 U/mL). Trace levels of activity were observed in culture 247. Conclusions. Strains 7, 20, 247, and 51, for the first time isolated from the Black Sea, are promising for further studies as producers of cellulase, β-mannanase, keratinase, and caseinolytic enzymes.
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Mikrobiolohichnyi zhurnal
Mikrobiolohichnyi zhurnal Medicine-Microbiology (medical)
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