Optimization of production of detergent-compatible and thrombolytic protease by Aspergillus flavus AT grown on agrowastes using Taguchi technique cum nanoparticles supplementation
{"title":"Optimization of production of detergent-compatible and thrombolytic protease by Aspergillus flavus AT grown on agrowastes using Taguchi technique cum nanoparticles supplementation","authors":"V.A. Ajayi, A. Lateef","doi":"10.1016/j.clcb.2025.100144","DOIUrl":null,"url":null,"abstract":"<div><div>Microbial proteases are important industrial enzymes with diverse applications. However, their production is expensive due to the cost of media, thereby necessitating the search for cheap substrates for their production. In this study, novel optimization regimen was applied to increase protease production by a local strain of <em>Aspergillus flavus</em> by deploying the Taguchi technique with the incorporation of ZnONPs. The isolate produced protease in both SmF and SSF by utilizing groundnut peel (GP), groundnut shell (GS) and melon seed shell (MS) with titers in the range of 24.20–45.65 U/ml for SmF and 18.15–152.90 U/g for SSF, respectively. Its protease production was further optimized in the underutilized MS, which has not been reported for protease production until now. Taguchi cum nanosupplemention in SmF increased protease production from 37.40–185.25 U/ml as the global optimum with the inclusion of ZnONPs accounting for up to 10.74 % of the production. The improved production of protease was 4.95 fold compared with the unoptimized bioprocess. The protease was effective for blood stain removing and showed enhanced proteolytic activities of 254.72–329.10 U/ml corresponding to performance of 137.50–177.65 % in the presence of four detergents indicating high level of compatibility. The protease also dissolved blood clot by 91.30 %, thereby making it useful as thrombolytic agent. For the first time, we report the microbial production of protease using MS-based media and enhanced its production via incorporation of nanoparticles. Thus, the detergent-compatible protease produced in this study has industrial and biomedical applications.</div></div>","PeriodicalId":100250,"journal":{"name":"Cleaner and Circular Bioeconomy","volume":"10 ","pages":"Article 100144"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cleaner and Circular Bioeconomy","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772801325000119","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Microbial proteases are important industrial enzymes with diverse applications. However, their production is expensive due to the cost of media, thereby necessitating the search for cheap substrates for their production. In this study, novel optimization regimen was applied to increase protease production by a local strain of Aspergillus flavus by deploying the Taguchi technique with the incorporation of ZnONPs. The isolate produced protease in both SmF and SSF by utilizing groundnut peel (GP), groundnut shell (GS) and melon seed shell (MS) with titers in the range of 24.20–45.65 U/ml for SmF and 18.15–152.90 U/g for SSF, respectively. Its protease production was further optimized in the underutilized MS, which has not been reported for protease production until now. Taguchi cum nanosupplemention in SmF increased protease production from 37.40–185.25 U/ml as the global optimum with the inclusion of ZnONPs accounting for up to 10.74 % of the production. The improved production of protease was 4.95 fold compared with the unoptimized bioprocess. The protease was effective for blood stain removing and showed enhanced proteolytic activities of 254.72–329.10 U/ml corresponding to performance of 137.50–177.65 % in the presence of four detergents indicating high level of compatibility. The protease also dissolved blood clot by 91.30 %, thereby making it useful as thrombolytic agent. For the first time, we report the microbial production of protease using MS-based media and enhanced its production via incorporation of nanoparticles. Thus, the detergent-compatible protease produced in this study has industrial and biomedical applications.