Purification and characterization of alkaline soda-bleach stable protease from Bacillus sp. APP-07 isolated from Laundromat soil

The detergent-compatible alkaline protease was produced from the bacterial strain Bacillus sp. APP-07 isolated from Laundromat soil of Solapur, Maharashtra, India. The culture was grown in 1000 ml capacity baffled flask with a working volume of 100 ml and incubated at 55 °C for 33 h on a rotary shak...

Full description

Bibliographic Details
Main Authors: I.K. Shaikh, P.P. Dixit, T.M. Shaikh
Format: Article
Language:English
Published: SpringerOpen 2018-12-01
Series:Journal of Genetic Engineering and Biotechnology
Online Access:http://www.sciencedirect.com/science/article/pii/S1687157X18300702
id doaj-b13d31ee90e54c3e824ba4b552df00d0
record_format Article
spelling doaj-b13d31ee90e54c3e824ba4b552df00d02020-11-25T02:20:50ZengSpringerOpenJournal of Genetic Engineering and Biotechnology1687-157X2018-12-01162273279Purification and characterization of alkaline soda-bleach stable protease from Bacillus sp. APP-07 isolated from Laundromat soilI.K. Shaikh0P.P. Dixit1T.M. Shaikh2Department of Microbiology, Dr. Babasaheb Ambedkar Marathwada University, Sub Campus, Osmanabad, India; Deparment of Antitoxin and Sera, Haffkine Biopharmaceutical Corporation Limited, Pune, IndiaDepartment of Microbiology, Dr. Babasaheb Ambedkar Marathwada University, Sub Campus, Osmanabad, India; Corresponding author at: Department of Microbiology, Dr. Babasaheb Ambedkar Marathwada University, Sub Campus, Osmanabad, 413501, India.Deparment of Antitoxin and Sera, Haffkine Biopharmaceutical Corporation Limited, Pune, IndiaThe detergent-compatible alkaline protease was produced from the bacterial strain Bacillus sp. APP-07 isolated from Laundromat soil of Solapur, Maharashtra, India. The culture was grown in 1000 ml capacity baffled flask with a working volume of 100 ml and incubated at 55 °C for 33 h on a rotary shaker. After incubation, alkaline protease was partially purified by the sequential method of acetone precipitation followed by nominal molecular weight limit (NMWL) cut-off ultrafiltration using 50 K and 10 K filters. Finally, Sephadex G-100 gel filtration chromatographic purification was performed to obtain 3.12 fold purified alkaline protease enzyme with a 66.67% final yield. The purified enzyme showed 31907.269 units (U) of enzyme activity containing 8741.718 U/mg of specific enzyme activity. The molecular weight of the enzyme was confirmed about 33.0 kDa (kDa) by the SDS-PAGE analysis. The purified enzyme was stable at higher pH and temperature range, with an optimum pH 10.5 and temperature 55 °C. The enzyme showed excellent stability and compatibility in various detergents, surfactants, bleach, and oxidizing agents. The enzyme activity enhanced in the presence of Ca2+, Cu2+, and surfactants, whereas; the phenylmethylsulphonyl fluoride (PMSF) and Diisopropyl fluorophosphate (DFP) completely inhibit the enzymatic activity, which pointed out that the enzyme affiliated to serine-centered metalloproteases family.In conclusion, the remarkable tolerance and stability of the enzyme explored the promising candidature for the several potential applications in the laundry detergents. The sustainability of the enzyme might serve several possible applications in the laundry detergents, leather industries, and other harsh industrial processes. Keywords: Bacillus sp., Alkaline protease, Purification and characterization, Laundry detergenthttp://www.sciencedirect.com/science/article/pii/S1687157X18300702
collection DOAJ
language English
format Article
sources DOAJ
author I.K. Shaikh
P.P. Dixit
T.M. Shaikh
spellingShingle I.K. Shaikh
P.P. Dixit
T.M. Shaikh
Purification and characterization of alkaline soda-bleach stable protease from Bacillus sp. APP-07 isolated from Laundromat soil
Journal of Genetic Engineering and Biotechnology
author_facet I.K. Shaikh
P.P. Dixit
T.M. Shaikh
author_sort I.K. Shaikh
title Purification and characterization of alkaline soda-bleach stable protease from Bacillus sp. APP-07 isolated from Laundromat soil
title_short Purification and characterization of alkaline soda-bleach stable protease from Bacillus sp. APP-07 isolated from Laundromat soil
title_full Purification and characterization of alkaline soda-bleach stable protease from Bacillus sp. APP-07 isolated from Laundromat soil
title_fullStr Purification and characterization of alkaline soda-bleach stable protease from Bacillus sp. APP-07 isolated from Laundromat soil
title_full_unstemmed Purification and characterization of alkaline soda-bleach stable protease from Bacillus sp. APP-07 isolated from Laundromat soil
title_sort purification and characterization of alkaline soda-bleach stable protease from bacillus sp. app-07 isolated from laundromat soil
publisher SpringerOpen
series Journal of Genetic Engineering and Biotechnology
issn 1687-157X
publishDate 2018-12-01
description The detergent-compatible alkaline protease was produced from the bacterial strain Bacillus sp. APP-07 isolated from Laundromat soil of Solapur, Maharashtra, India. The culture was grown in 1000 ml capacity baffled flask with a working volume of 100 ml and incubated at 55 °C for 33 h on a rotary shaker. After incubation, alkaline protease was partially purified by the sequential method of acetone precipitation followed by nominal molecular weight limit (NMWL) cut-off ultrafiltration using 50 K and 10 K filters. Finally, Sephadex G-100 gel filtration chromatographic purification was performed to obtain 3.12 fold purified alkaline protease enzyme with a 66.67% final yield. The purified enzyme showed 31907.269 units (U) of enzyme activity containing 8741.718 U/mg of specific enzyme activity. The molecular weight of the enzyme was confirmed about 33.0 kDa (kDa) by the SDS-PAGE analysis. The purified enzyme was stable at higher pH and temperature range, with an optimum pH 10.5 and temperature 55 °C. The enzyme showed excellent stability and compatibility in various detergents, surfactants, bleach, and oxidizing agents. The enzyme activity enhanced in the presence of Ca2+, Cu2+, and surfactants, whereas; the phenylmethylsulphonyl fluoride (PMSF) and Diisopropyl fluorophosphate (DFP) completely inhibit the enzymatic activity, which pointed out that the enzyme affiliated to serine-centered metalloproteases family.In conclusion, the remarkable tolerance and stability of the enzyme explored the promising candidature for the several potential applications in the laundry detergents. The sustainability of the enzyme might serve several possible applications in the laundry detergents, leather industries, and other harsh industrial processes. Keywords: Bacillus sp., Alkaline protease, Purification and characterization, Laundry detergent
url http://www.sciencedirect.com/science/article/pii/S1687157X18300702
work_keys_str_mv AT ikshaikh purificationandcharacterizationofalkalinesodableachstableproteasefrombacillusspapp07isolatedfromlaundromatsoil
AT ppdixit purificationandcharacterizationofalkalinesodableachstableproteasefrombacillusspapp07isolatedfromlaundromatsoil
AT tmshaikh purificationandcharacterizationofalkalinesodableachstableproteasefrombacillusspapp07isolatedfromlaundromatsoil
_version_ 1724869381732696064