Pectinase production by fungal-based solid-state fermentation of selected agricultural wastes

S. Awe, A. Ajiboye, F. Agboola
{"title":"Pectinase production by fungal-based solid-state fermentation of selected agricultural wastes","authors":"S. Awe, A. Ajiboye, F. Agboola","doi":"10.31248/jbbd2023.179","DOIUrl":null,"url":null,"abstract":"Agricultural waste is the residues from growing and processing raw agricultural products. They can be properly managed using fungi to produce economical materials such as pectinase enzymes that act as biological agents which are applicable in many areas. This research was aimed at producing pectinase by fungal-based solid-state fermentation of agricultural wastes. Fungi were isolated from dump sites soil using the pour plate method. These fungal isolates were inoculated into the pretreated agricultural waste, including watermelon, mango, and pineapple peels. The degradation period was 15 days on mineral salt solid media using separate flasks for each waste and fungus. They were incubated at room temperature (28°C). The pectinase was assayed using pectin and DNSA (dinitrosalicyclic acid). Fungal isolates were identified and screened for pectinase production using standard methods. The pH and temperature were optimized to study the effect on pectinase activities using standard procedures and pectinase was purified using column sephadex G-100. Molecular identifications were carried out on the isolates using 18srRNA gene primers. The fungi were identified as Aspergillus niger strain AGF3 (OM273994), Penicillium Chrysogenum strain AGF2 (OM273982) and Cladosporium tenuissimum strain AGF1 (OM273981). Aspergillus niger strain AGF3 (OM273994) produced the highest specific pectinase activities in mango waste (2400 U/mg. protein/ mL and it can be compared to what was produced by Cladosporium tenuissimum strain AGF1 (OM273981) (1590 U/mg. protein/mL). High specific pecrtinase activity was also obtained from pineapple peels (2200 U/mg. protein/mL) produced by Cladosporium tenussimum strain AGF1 (OM273981). It can be concluded in this study that Aspergillus niger strain AGF3 (OM273994) and Cladosporium tenuissimum strain AGF1 (OM273981) were the best producers of pectinase using mango and pineapple peels, while Penicillium chrysogenum strain AGF2 (OM273982) produced substantial pectinase in all the three agricultural wastes but not at higher levels.","PeriodicalId":15121,"journal":{"name":"Journal of Bioscience and Biotechnology Discovery","volume":"167 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bioscience and Biotechnology Discovery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31248/jbbd2023.179","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

Agricultural waste is the residues from growing and processing raw agricultural products. They can be properly managed using fungi to produce economical materials such as pectinase enzymes that act as biological agents which are applicable in many areas. This research was aimed at producing pectinase by fungal-based solid-state fermentation of agricultural wastes. Fungi were isolated from dump sites soil using the pour plate method. These fungal isolates were inoculated into the pretreated agricultural waste, including watermelon, mango, and pineapple peels. The degradation period was 15 days on mineral salt solid media using separate flasks for each waste and fungus. They were incubated at room temperature (28°C). The pectinase was assayed using pectin and DNSA (dinitrosalicyclic acid). Fungal isolates were identified and screened for pectinase production using standard methods. The pH and temperature were optimized to study the effect on pectinase activities using standard procedures and pectinase was purified using column sephadex G-100. Molecular identifications were carried out on the isolates using 18srRNA gene primers. The fungi were identified as Aspergillus niger strain AGF3 (OM273994), Penicillium Chrysogenum strain AGF2 (OM273982) and Cladosporium tenuissimum strain AGF1 (OM273981). Aspergillus niger strain AGF3 (OM273994) produced the highest specific pectinase activities in mango waste (2400 U/mg. protein/ mL and it can be compared to what was produced by Cladosporium tenuissimum strain AGF1 (OM273981) (1590 U/mg. protein/mL). High specific pecrtinase activity was also obtained from pineapple peels (2200 U/mg. protein/mL) produced by Cladosporium tenussimum strain AGF1 (OM273981). It can be concluded in this study that Aspergillus niger strain AGF3 (OM273994) and Cladosporium tenuissimum strain AGF1 (OM273981) were the best producers of pectinase using mango and pineapple peels, while Penicillium chrysogenum strain AGF2 (OM273982) produced substantial pectinase in all the three agricultural wastes but not at higher levels.
选定农业废弃物的真菌固态发酵生产果胶酶
农业废弃物是种植和加工农产品的残留物。利用真菌可以适当地管理它们,以生产经济的材料,如果胶酶,作为生物制剂,可适用于许多领域。本研究旨在利用真菌为基础的农业废弃物固态发酵生产果胶酶。采用倾板法从垃圾场土壤中分离真菌。将这些真菌分离株接种到预处理的农业废弃物中,包括西瓜、芒果和菠萝皮。在矿物盐固体培养基上,每一种废弃物和真菌分别用不同的烧瓶进行降解,降解期为15 d。室温(28℃)培养。用果胶和二硝基水杨酸测定果胶酶。采用标准方法对分离的真菌进行鉴定和筛选,以生产果胶酶。采用标准程序优化pH和温度对果胶酶活性的影响,并用sephadex G-100柱对果胶酶进行纯化。利用18srRNA基因引物对分离株进行分子鉴定。真菌鉴定为黑曲霉菌株AGF3 (OM273994)、青霉菌菌株AGF2 (OM273982)和细枝霉菌株AGF1 (OM273981)。黑曲霉菌株AGF3 (OM273994)在芒果废弃物中产生的比果胶酶活性最高(2400 U/mg)。蛋白/ mL,可与枯枝孢菌AGF1 (OM273981)产生的1590 U/mg相比较。蛋白质/毫升)。菠萝果胶酶活性也较高(2200 U/mg)。蛋白/mL),由tenussimum枝孢菌AGF1 (OM273981)产生。本研究结果表明,黑曲霉AGF3 (OM273994)和柔韧枝孢杆菌AGF1 (OM273981)是利用芒果和菠萝果皮产生果胶酶最好的菌株,而青霉菌AGF2 (OM273982)在三种农业废弃物中均产生大量果胶酶,但含量不高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信