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Optimization of protease production from Rhizomucor miehei Rm4 isolate under solid-state fermentation

BACKGROUND: Protease is one of the most important industrial enzymes. The importance of protease bioproduction comes from meeting the increasing demand for this enzyme especially in the cheese industry. Rhizomucor miehei protease is the preferred substitute for the traditional rennet. Solid-state fe...

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Autores principales: Alahmad Aljammas, Houthail, Yazji, Sabah, Azizieh, Abdulhakim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9151939/
https://www.ncbi.nlm.nih.gov/pubmed/35635657
http://dx.doi.org/10.1186/s43141-022-00358-9
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author Alahmad Aljammas, Houthail
Yazji, Sabah
Azizieh, Abdulhakim
author_facet Alahmad Aljammas, Houthail
Yazji, Sabah
Azizieh, Abdulhakim
author_sort Alahmad Aljammas, Houthail
collection PubMed
description BACKGROUND: Protease is one of the most important industrial enzymes. The importance of protease bioproduction comes from meeting the increasing demand for this enzyme especially in the cheese industry. Rhizomucor miehei protease is the preferred substitute for the traditional rennet. Solid-state fermentation (SSF) shows promising results in enzyme production. An optimization strategy was applied to optimize the production of Rhizomucor miehei protease in a solid medium. The components of the fermentation medium were screened by using the one-factor-at-a-time (OFAT) approach. The optimization process then was performed by using the response surface methodology (RSM) approach based on five factors (fermentation time, temperature, pH, moisture content, nitrogen concentration) at five levels. Specific milk clotting activity and milk clotting activity/proteolytic activity ratio were considered as response variables in the optimization process. RESULTS: Among several combinations, wheat bran was selected as the best substrate. Casein was selected based on preliminary screening of nitrogen sources. The optimal conditions identified by RSM analysis were found to be 81.21 h, 41.11°C, 6.31, 80%, and 1.33% for fermentation time, temperature, pH, moisture content, and casein concentration, respectively. The performed fermentation process under the optimized conditions gave an enzymatic extract with the values of 5.11 mg/mL, 2258.13 Soxhlet unit/mL, 441.90 Soxhlet unit/mg, 1.14 protease unit/mg, and 388.66 for protein content, milk clotting activity, specific clotting activity, specific proteolytic activity, and milk clotting activity/proteolytic activity ratio, respectively. The aforementioned values were close to the predicted values. CONCLUSION: The high milk clotting activity and the relatively low proteolytic activity signify higher specificity of the produced enzyme, which is favorable in cheese making. The observed results reveal the efficiency of the applied statistical approaches in obtaining desired values of response variables and minimizing experimental runs, as well as achieving good predictions for response variables.
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spelling pubmed-91519392022-06-16 Optimization of protease production from Rhizomucor miehei Rm4 isolate under solid-state fermentation Alahmad Aljammas, Houthail Yazji, Sabah Azizieh, Abdulhakim J Genet Eng Biotechnol Research BACKGROUND: Protease is one of the most important industrial enzymes. The importance of protease bioproduction comes from meeting the increasing demand for this enzyme especially in the cheese industry. Rhizomucor miehei protease is the preferred substitute for the traditional rennet. Solid-state fermentation (SSF) shows promising results in enzyme production. An optimization strategy was applied to optimize the production of Rhizomucor miehei protease in a solid medium. The components of the fermentation medium were screened by using the one-factor-at-a-time (OFAT) approach. The optimization process then was performed by using the response surface methodology (RSM) approach based on five factors (fermentation time, temperature, pH, moisture content, nitrogen concentration) at five levels. Specific milk clotting activity and milk clotting activity/proteolytic activity ratio were considered as response variables in the optimization process. RESULTS: Among several combinations, wheat bran was selected as the best substrate. Casein was selected based on preliminary screening of nitrogen sources. The optimal conditions identified by RSM analysis were found to be 81.21 h, 41.11°C, 6.31, 80%, and 1.33% for fermentation time, temperature, pH, moisture content, and casein concentration, respectively. The performed fermentation process under the optimized conditions gave an enzymatic extract with the values of 5.11 mg/mL, 2258.13 Soxhlet unit/mL, 441.90 Soxhlet unit/mg, 1.14 protease unit/mg, and 388.66 for protein content, milk clotting activity, specific clotting activity, specific proteolytic activity, and milk clotting activity/proteolytic activity ratio, respectively. The aforementioned values were close to the predicted values. CONCLUSION: The high milk clotting activity and the relatively low proteolytic activity signify higher specificity of the produced enzyme, which is favorable in cheese making. The observed results reveal the efficiency of the applied statistical approaches in obtaining desired values of response variables and minimizing experimental runs, as well as achieving good predictions for response variables. Springer Berlin Heidelberg 2022-05-30 /pmc/articles/PMC9151939/ /pubmed/35635657 http://dx.doi.org/10.1186/s43141-022-00358-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Alahmad Aljammas, Houthail
Yazji, Sabah
Azizieh, Abdulhakim
Optimization of protease production from Rhizomucor miehei Rm4 isolate under solid-state fermentation
title Optimization of protease production from Rhizomucor miehei Rm4 isolate under solid-state fermentation
title_full Optimization of protease production from Rhizomucor miehei Rm4 isolate under solid-state fermentation
title_fullStr Optimization of protease production from Rhizomucor miehei Rm4 isolate under solid-state fermentation
title_full_unstemmed Optimization of protease production from Rhizomucor miehei Rm4 isolate under solid-state fermentation
title_short Optimization of protease production from Rhizomucor miehei Rm4 isolate under solid-state fermentation
title_sort optimization of protease production from rhizomucor miehei rm4 isolate under solid-state fermentation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9151939/
https://www.ncbi.nlm.nih.gov/pubmed/35635657
http://dx.doi.org/10.1186/s43141-022-00358-9
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