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海洋酵母正假丝酵母AKB-1产生的碱性蛋白酶的特性及其应用

Characterization of alkaline protease enzyme produced from marine yeast Candida orthopsilosis AKB-1 and its applications.

作者信息

Sarkar Anwesha, S R Anjukrishna, K V Bhaskara Rao

机构信息

Marine Biotechnology Laboratory, Department of Biomedical Sciences, School of Biosciences and Technology, Vellore Institute of Technology, Vellore, 632014, Tamil Nadu, India.

出版信息

Folia Microbiol (Praha). 2024 Oct 28. doi: 10.1007/s12223-024-01216-6.

Abstract

The present study has undertaken the isolation of marine yeasts from mangrove sediment samples and their ability to produce alkaline protease enzymes. A total of 14 yeast isolates were recovered on yeast-malt agar (YMA) and yeast extract peptone dextrose (YEPD) agar medium. After screening for proteolytic activity on skim milk agar, marine yeast isolate, AKB-1 exhibited a hydrolysis zone of 18 mm. Optimal conditions for the enzyme production from yeast isolate AKB-1 were at 30 °C, pH 8, fructose as carbon source, potassium nitrate as nitrogen source, and 25% saline concentration. Under the optimal conditions, the protease enzyme activity of the isolate AKB-1 was observed to be 978 IU/mL. The structural and functional analysis was carried out through FTIR and HPLC analysis for the extracted protease enzyme. Furthermore, the enzyme produced was partially purified by solvent extraction using ethyl acetate and ammonium sulfate precipitation (3.4-fold) followed by dialysis (56.8-fold). The molecular weight of the purified enzyme was observed to be around 60 kDa using SDS-PAGE. The extracted protein showed good antibacterial activity against six different clinical bacterial pathogens and the highest against Bacillus cereus (16 ± 0.5 mm). The extracted protease enzyme was revealed to remove blood stains from cloth within 20 min of application similar to the commercial detergent. The marine yeast isolate was further identified as Candida orthopsilosis AKB-1 (Accession number KY348766) through 18S rRNA sequencing, and a phylogenetic tree was generated.

摘要

本研究从红树林沉积物样本中分离出海洋酵母,并研究了它们产生碱性蛋白酶的能力。在酵母麦芽琼脂(YMA)和酵母提取物蛋白胨葡萄糖(YEPD)琼脂培养基上共分离出14株酵母菌株。在脱脂乳琼脂上筛选蛋白水解活性后,海洋酵母菌株AKB-1表现出18毫米的水解圈。酵母菌株AKB-1产生酶的最佳条件为30℃、pH 8、以果糖为碳源、硝酸钾为氮源以及25%的盐浓度。在最佳条件下,观察到菌株AKB-1的蛋白酶活性为978 IU/mL。通过傅里叶变换红外光谱(FTIR)和高效液相色谱(HPLC)分析对提取的蛋白酶进行了结构和功能分析。此外,所产生的酶通过乙酸乙酯溶剂萃取和硫酸铵沉淀(3.4倍)进行部分纯化,随后进行透析(56.8倍)。使用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)观察到纯化酶的分子量约为60 kDa。提取的蛋白质对六种不同的临床细菌病原体表现出良好的抗菌活性,对蜡样芽孢杆菌的抗菌活性最高(16±0.5毫米)。结果表明,所提取的蛋白酶在应用20分钟内即可去除布料上的血迹,效果与商用洗涤剂类似。通过18S rRNA测序进一步将该海洋酵母菌株鉴定为正假丝酵母AKB-1(登录号KY348766),并构建了系统发育树。

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