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Isolation and screening of Streptomyces sp. Al-Dhabi-49 from the environment of Saudi Arabia with concomitant production of lipase and protease in submerged fermentation

In this study, Streptomyces sp. Al-Dhabi-49 was isolated from the soil sample of Saudi Arabian environment for the simultaneous production of lipase and protease in submerged fermentation. The process parameters were optimized to enhance enzymes production. The production of protease and lipase was...

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Autores principales: Al-Dhabi, Naif Abdullah, Esmail, Galal Ali, Ghilan, Abdul-Kareem Mohammed, Arasu, Mariadhas Valan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933164/
https://www.ncbi.nlm.nih.gov/pubmed/31889873
http://dx.doi.org/10.1016/j.sjbs.2019.11.011
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author Al-Dhabi, Naif Abdullah
Esmail, Galal Ali
Ghilan, Abdul-Kareem Mohammed
Arasu, Mariadhas Valan
author_facet Al-Dhabi, Naif Abdullah
Esmail, Galal Ali
Ghilan, Abdul-Kareem Mohammed
Arasu, Mariadhas Valan
author_sort Al-Dhabi, Naif Abdullah
collection PubMed
description In this study, Streptomyces sp. Al-Dhabi-49 was isolated from the soil sample of Saudi Arabian environment for the simultaneous production of lipase and protease in submerged fermentation. The process parameters were optimized to enhance enzymes production. The production of protease and lipase was found to be maximum after 5 days of incubation (139.2 ± 2.1 U/ml, 253 ± 4.4 U/ml). Proteolytic enzyme increases with the increase in pH up to 9.0 (147.2 ± 3.6 U/ml) and enzyme production depleted significantly at higher pH values. In the case of lipase, production was maximum in the culture medium containing pH 8.0 (166 ± 1.3 U/ml). The maximum production of protease was observed at 40 °C (174 ± 12.1 U/ml) by Streptomyces sp. Lipase activity was found to be optimum at the range of temperatures (30–50 °C) and maximum production was achieved at 35 °C (168 ± 7.8 U/ml). Among the evaluated carbon sources, maltose significantly influenced on protease production (218 ± 12.8 U/ml). Lipase production was maximum when Streptomyces sp. was cultured in the presence of glucose (162 ± 10.8U/ml). Among various concentrations of peptone, 1.0% (w/v) significantly enhanced protease production. The lipase production was very high in the culture medium containing malt extract as nitrogen source (86 ± 10.2 U/ml). Protease production was maximum in the presence of Ca(2+) as ionic source (212 ± 3.8 U/ml) and lipase production was enhanced by the addition of Mg(2+) with the fermentation medium (163.7 ± 6.2 U/ml).
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spelling pubmed-69331642019-12-30 Isolation and screening of Streptomyces sp. Al-Dhabi-49 from the environment of Saudi Arabia with concomitant production of lipase and protease in submerged fermentation Al-Dhabi, Naif Abdullah Esmail, Galal Ali Ghilan, Abdul-Kareem Mohammed Arasu, Mariadhas Valan Saudi J Biol Sci Article In this study, Streptomyces sp. Al-Dhabi-49 was isolated from the soil sample of Saudi Arabian environment for the simultaneous production of lipase and protease in submerged fermentation. The process parameters were optimized to enhance enzymes production. The production of protease and lipase was found to be maximum after 5 days of incubation (139.2 ± 2.1 U/ml, 253 ± 4.4 U/ml). Proteolytic enzyme increases with the increase in pH up to 9.0 (147.2 ± 3.6 U/ml) and enzyme production depleted significantly at higher pH values. In the case of lipase, production was maximum in the culture medium containing pH 8.0 (166 ± 1.3 U/ml). The maximum production of protease was observed at 40 °C (174 ± 12.1 U/ml) by Streptomyces sp. Lipase activity was found to be optimum at the range of temperatures (30–50 °C) and maximum production was achieved at 35 °C (168 ± 7.8 U/ml). Among the evaluated carbon sources, maltose significantly influenced on protease production (218 ± 12.8 U/ml). Lipase production was maximum when Streptomyces sp. was cultured in the presence of glucose (162 ± 10.8U/ml). Among various concentrations of peptone, 1.0% (w/v) significantly enhanced protease production. The lipase production was very high in the culture medium containing malt extract as nitrogen source (86 ± 10.2 U/ml). Protease production was maximum in the presence of Ca(2+) as ionic source (212 ± 3.8 U/ml) and lipase production was enhanced by the addition of Mg(2+) with the fermentation medium (163.7 ± 6.2 U/ml). Elsevier 2020-01 2019-11-22 /pmc/articles/PMC6933164/ /pubmed/31889873 http://dx.doi.org/10.1016/j.sjbs.2019.11.011 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Al-Dhabi, Naif Abdullah
Esmail, Galal Ali
Ghilan, Abdul-Kareem Mohammed
Arasu, Mariadhas Valan
Isolation and screening of Streptomyces sp. Al-Dhabi-49 from the environment of Saudi Arabia with concomitant production of lipase and protease in submerged fermentation
title Isolation and screening of Streptomyces sp. Al-Dhabi-49 from the environment of Saudi Arabia with concomitant production of lipase and protease in submerged fermentation
title_full Isolation and screening of Streptomyces sp. Al-Dhabi-49 from the environment of Saudi Arabia with concomitant production of lipase and protease in submerged fermentation
title_fullStr Isolation and screening of Streptomyces sp. Al-Dhabi-49 from the environment of Saudi Arabia with concomitant production of lipase and protease in submerged fermentation
title_full_unstemmed Isolation and screening of Streptomyces sp. Al-Dhabi-49 from the environment of Saudi Arabia with concomitant production of lipase and protease in submerged fermentation
title_short Isolation and screening of Streptomyces sp. Al-Dhabi-49 from the environment of Saudi Arabia with concomitant production of lipase and protease in submerged fermentation
title_sort isolation and screening of streptomyces sp. al-dhabi-49 from the environment of saudi arabia with concomitant production of lipase and protease in submerged fermentation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933164/
https://www.ncbi.nlm.nih.gov/pubmed/31889873
http://dx.doi.org/10.1016/j.sjbs.2019.11.011
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