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Alkaline Protease Production from Bacillus gibsonii 6BS15-4 Using Dairy Effluent and Its Characterization as a Laundry Detergent Additive
Protease is a widely used enzyme particularly in the detergent industry. In this research, we aimed to isolate alkaline protease-producing bacteria for characterization as a laundry detergent additive. The screening of alkaline protease production was investigated on basal medium agar plus 1% skim m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Microbiology and Biotechnology
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998202/ https://www.ncbi.nlm.nih.gov/pubmed/36697226 http://dx.doi.org/10.4014/jmb.2210.10007 |
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author | Mahakhan, Polson Apiso, Patapee Srisunthorn, Kannika Vichitphan, Kanit Vichitphan, Sukanda Punyauppa-path, Sukrita Sawaengkaew, Jutaporn |
author_facet | Mahakhan, Polson Apiso, Patapee Srisunthorn, Kannika Vichitphan, Kanit Vichitphan, Sukanda Punyauppa-path, Sukrita Sawaengkaew, Jutaporn |
author_sort | Mahakhan, Polson |
collection | PubMed |
description | Protease is a widely used enzyme particularly in the detergent industry. In this research, we aimed to isolate alkaline protease-producing bacteria for characterization as a laundry detergent additive. The screening of alkaline protease production was investigated on basal medium agar plus 1% skim milk at pH 11, with incubation at 30°C. The highest alkaline protease-producing bacterium was 6BS15-4 strain, identified as Bacillus gibsonii by 16S rRNA gene sequencing. While the optimum pH was 12.0, the strain was stable at pH range 7.0-12.0 when incubated at 45°C for 60 min. The alkaline protease produced by B. gibsonii 6BS15-4 using dairy effluent was characterized. The optimum temperature was 60°C and the enzyme was stable at 55°C when incubated at pH 11.0 for 60 min. Metal ions K(+), Mg(2+), Cu(2+), Na(+), and Zn(2+) exhibited a slightly stimulatory effect on enzyme activity. The enzyme retained over 80% of its activity in the presence of Ca(2+), Ba(2+), and Mn(2+). Thiol reagent and ethylenediaminetetraacetic acid did not inhibit the enzyme activity, whereas phenylmethylsulfonyl fluoride significantly inhibited the protease activity. The alkaline protease from B. gibsonii 6BS15-4 demonstrated efficiency in blood stain removal and could therefore be used as a detergent additive, with potential for various other industrial applications. |
format | Online Article Text |
id | pubmed-9998202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Korean Society for Microbiology and Biotechnology |
record_format | MEDLINE/PubMed |
spelling | pubmed-99982022023-03-10 Alkaline Protease Production from Bacillus gibsonii 6BS15-4 Using Dairy Effluent and Its Characterization as a Laundry Detergent Additive Mahakhan, Polson Apiso, Patapee Srisunthorn, Kannika Vichitphan, Kanit Vichitphan, Sukanda Punyauppa-path, Sukrita Sawaengkaew, Jutaporn J Microbiol Biotechnol Research article Protease is a widely used enzyme particularly in the detergent industry. In this research, we aimed to isolate alkaline protease-producing bacteria for characterization as a laundry detergent additive. The screening of alkaline protease production was investigated on basal medium agar plus 1% skim milk at pH 11, with incubation at 30°C. The highest alkaline protease-producing bacterium was 6BS15-4 strain, identified as Bacillus gibsonii by 16S rRNA gene sequencing. While the optimum pH was 12.0, the strain was stable at pH range 7.0-12.0 when incubated at 45°C for 60 min. The alkaline protease produced by B. gibsonii 6BS15-4 using dairy effluent was characterized. The optimum temperature was 60°C and the enzyme was stable at 55°C when incubated at pH 11.0 for 60 min. Metal ions K(+), Mg(2+), Cu(2+), Na(+), and Zn(2+) exhibited a slightly stimulatory effect on enzyme activity. The enzyme retained over 80% of its activity in the presence of Ca(2+), Ba(2+), and Mn(2+). Thiol reagent and ethylenediaminetetraacetic acid did not inhibit the enzyme activity, whereas phenylmethylsulfonyl fluoride significantly inhibited the protease activity. The alkaline protease from B. gibsonii 6BS15-4 demonstrated efficiency in blood stain removal and could therefore be used as a detergent additive, with potential for various other industrial applications. The Korean Society for Microbiology and Biotechnology 2023-02-28 2022-12-27 /pmc/articles/PMC9998202/ /pubmed/36697226 http://dx.doi.org/10.4014/jmb.2210.10007 Text en Copyright © 2023 by the authors. Licensee KMB. https://creativecommons.org/licenses/by/4.0/This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research article Mahakhan, Polson Apiso, Patapee Srisunthorn, Kannika Vichitphan, Kanit Vichitphan, Sukanda Punyauppa-path, Sukrita Sawaengkaew, Jutaporn Alkaline Protease Production from Bacillus gibsonii 6BS15-4 Using Dairy Effluent and Its Characterization as a Laundry Detergent Additive |
title | Alkaline Protease Production from Bacillus gibsonii 6BS15-4 Using Dairy Effluent and Its Characterization as a Laundry Detergent Additive |
title_full | Alkaline Protease Production from Bacillus gibsonii 6BS15-4 Using Dairy Effluent and Its Characterization as a Laundry Detergent Additive |
title_fullStr | Alkaline Protease Production from Bacillus gibsonii 6BS15-4 Using Dairy Effluent and Its Characterization as a Laundry Detergent Additive |
title_full_unstemmed | Alkaline Protease Production from Bacillus gibsonii 6BS15-4 Using Dairy Effluent and Its Characterization as a Laundry Detergent Additive |
title_short | Alkaline Protease Production from Bacillus gibsonii 6BS15-4 Using Dairy Effluent and Its Characterization as a Laundry Detergent Additive |
title_sort | alkaline protease production from bacillus gibsonii 6bs15-4 using dairy effluent and its characterization as a laundry detergent additive |
topic | Research article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998202/ https://www.ncbi.nlm.nih.gov/pubmed/36697226 http://dx.doi.org/10.4014/jmb.2210.10007 |
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