Majithiya Vaishali R, Gohel Sangeeta D
Department of Biosciences, Saurashtra University, Rajkot, 360005, Gujarat, India.
Appl Biochem Biotechnol. 2025 Jan;197(1):545-569. doi: 10.1007/s12010-024-05057-4. Epub 2024 Aug 29.
The oceanic actinobacteria have strong potential to secrete novel enzymes with unique properties useful for biotechnological applications. The Nocardiopsis dassonvillei strain VCS-4, associated with seaweed Caulerpa scalpeliformis, was a halo-alkaline protease producer. Further investigation focuses on medium optimization and the use of agro-industrial waste for economically feasible, high-yield protease production. A total of 12 experimental runs were designed using Minitab-20 software and Placket-Burman design. Among the 7 physicochemical parameters analyzed, incubation time and gelatin were detected as significant factors responsible for higher protease production. Incubation time and gelatin were further analyzed using OVATs. Optimal protease production was achieved with 2% gelatin, 0.1% yeast extract, 0.1% bacteriological peptone, 7% NaCl, pH 8, 5% inoculum, and a 7-day incubation period, resulting in a maximum protease activity (Pmax) of 363.97 U/mL, generation time of 11.9 h, specific growth rate of 0.161 g/mL/h, and protease productivity (Qp) of 61.65 U/mL/h. Moreover, utilizing groundnut cake as an agro-industrial waste led to enhanced production parameters: Pmax of 408.42 U/mL, generation time of 9.74 h, specific growth rate of 0.361 g/mL/h, and Qp of 68.07 U/mL/h. The immobilization of crude protease was achieved using Seralite SRC 120 as a support matrix resulting in 470.38 U/g immobilization, 88.20% immobilization yield, and 28.90% recovery activity. Characterization of both crude and immobilized proteases revealed optimal activity at pH 10 and 70 °C. Immobilization enhanced the shelf-life, reusability, and stability of VCS-4 protease under extreme conditions.
海洋放线菌具有强大的潜力,能够分泌具有独特性质的新型酶,这些酶对生物技术应用很有用。与海藻粗枝软骨藻相关的达松维尔诺卡氏菌菌株VCS-4是一种嗜盐碱性蛋白酶产生菌。进一步的研究集中在培养基优化以及利用农业工业废弃物实现经济可行的高产蛋白酶生产。使用Minitab-20软件和Plackett-Burman设计共设计了12次实验运行。在分析的7个理化参数中,培养时间和明胶被检测为导致更高蛋白酶产量的显著因素。使用一次一因子法对培养时间和明胶进行了进一步分析。在2%明胶、0.1%酵母提取物、0.1%细菌蛋白胨、7%氯化钠、pH 8、5%接种量和7天培养期的条件下实现了最佳蛋白酶生产,最大蛋白酶活性(Pmax)为363.97 U/mL,代时为11.9小时,比生长速率为0.161 g/mL/h,蛋白酶生产力(Qp)为61.65 U/mL/h。此外,利用花生饼作为农业工业废弃物可提高生产参数:Pmax为408.42 U/mL,代时为9.74小时,比生长速率为0.361 g/mL/h,Qp为68.07 U/mL/h。使用Seralite SRC 120作为支持基质实现了粗蛋白酶的固定化,固定化量为470.38 U/g,固定化产率为88.20%,回收活性为28.90%。对粗蛋白酶和固定化蛋白酶的表征显示,在pH 10和70°C下具有最佳活性。固定化提高了VCS-4蛋白酶在极端条件下的保质期、可重复使用性和稳定性。