Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/14487
Title: <span style="font-size:11.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-bidi-font-family: Mangal;mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language: HI" lang="EN-GB">Alkaline protease production, extraction and characterization from alkaliphilic <i style="mso-bidi-font-style:normal">Bacillus licheniformis</i> KBDL4: A Lonar soda lake isolate</span>
Authors: Pathak, Anupama P
Deshmukh, Kshipra B
Keywords: Alkaline protease
<i style="mso-bidi-font-style:normal"><span style="font-size:9.0pt;font-family:"Times New Roman";mso-fareast-font-family: "Times New Roman";mso-bidi-font-family:Mangal;letter-spacing:-.1pt;mso-ansi-language: EN-GB;mso-fareast-language:EN-US;mso-bidi-language:HI" lang="EN-GB">Bacillus licheniformis</span></i>
Gelatinous coating
Detergent compatibility
Lonar soda lake
Issue Date: Aug-2012
Publisher: NISCAIR-CSIR, India
Abstract: A bacterium producing an alkaline protease was isolated from the Lonar soda lake, Buldhana district (19°58' N; 76°31' E), Maharashtra, India. The most appropriate medium for the growth and protease production was composed of (g/L): casein 10; yeast extract 4; KH<sub>2</sub>PO<sub>4</sub> 0.5, K<sub>2</sub>HPO<sub>4</sub> 0.5 and CaCl<sub>2 </sub>0.5. The enzyme showed maximum activity with and without 5 m<i style="mso-bidi-font-style: normal">M</i> Ca<sup>2+</sup> at 70 and 60 <sup>o</sup>C, respectively. The enzyme retained 40 and 82% of its initial activity after heating for 60 min at 60 <sup>o</sup>C, in absence and presence of 5 m<i style="mso-bidi-font-style:normal">M</i> CaCl<sub>2 </sub>respectively. The enzyme remained active and stable at <i style="mso-bidi-font-style:normal">p</i>H 8-12, with an optimum at <i style="mso-bidi-font-style:normal">p</i>H 10. The enzyme showed stability towards non-ionic and anionic surfactants, and oxidizing agents. It also showed excellent stability and compatibility with commonly used laundry detergents. Wash performance analysis revealed that enzyme could effectively remove blood stains. It also showed decomposition of gelatinous coating on X- ray film.
Description: 569-576
URI: http://hdl.handle.net/123456789/14487
ISSN: 0975-1009 (Online); 0019-5189 (Print)
Appears in Collections:IJEB Vol.50(08) [August 2012]

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