Purification and characterization of a cold active alkaline protease from Stenotrophomonas sp., isolated from Kashmir, India

被引:28
|
作者
Saba, Iram [1 ]
Qazi, Parvaiz H. [1 ]
Rather, Shabir A. [1 ]
Dar, Refaz A. [1 ]
Qadri, Qurrat A. [1 ]
Ahmad, Nasier [1 ]
Johri, Sarojini [2 ]
Taneja, Subash C. [3 ]
Shawl, Sami [4 ]
机构
[1] Indian Inst Integrat Med, Div Biotechnol, Council Sci & Ind Res, Srinagar 190005, Jammu & Kashmir, India
[2] Indian Inst Integrat Med, Div Biotechnol, Council Sci & Ind Res, Jammu 190008, India
[3] Indian Inst Integrat Med, Bioorgan Chem Div, Council Sci & Ind Res, Jammu 190008, India
[4] Indian Inst Integrat Med, Div Chem, Council Sci & Ind Res, Srinagar 190005, Jammu & Kashmir, India
来源
关键词
Psychrotolerant; Cold active enzyme; Alkaline protease; OPTIMIZATION; ENZYMES; DNA;
D O I
10.1007/s11274-011-0905-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A Psychrotolerant alkaline protease producing bacterium IIIM-ST045 was isolated from a soil sample collected from the Thajiwas glacier of Kashmir, India and identified as Stenotrophomonas sp. on the basis of its biochemical properties and 16S ribosomal gene sequencing. The strain could grow well within a temperature range of 4-37A degrees C however, showed optimum growth at 15A degrees C. The strain was found to over-produce proteases when it was grown in media containing lactose as carbon source (157.50 U mg(-1)). The maximum specific enzyme activity (398 U mg(-1)) was obtained using soya oil as nitrogen source, however, the inorganic nitrogen sources urea, ammonium chloride and ammonium sulphate showed the lowest production of 38.9, 62.2 and 57.9 U mg(-1). The enzyme was purified to 18.45 folds and the molecular weight of the partially purified protease was estimated to be similar to 55 kDa by SDS-PAGE analysis. The protease activity increased as the increase in enzyme concentration while as the optimum enzyme activity was found when casein (1% w/v) was used as substrate. The enzyme was highly active over a wide range of pH from 6.5 to 12.0 showing optimum activity at pH 10.0. The optimum temperature for the enzyme was 15A degrees C. Proteolytic activity reduced gradually with higher temperatures with a decrease of 56% at 40A degrees C. The purified enzyme was checked for the removal of protein containing tea stains using a silk cloth within a temperature range of 10-60A degrees C. The best washing efficiency results obtained at low temperatures indicate that the enzyme may be used for cold washing purposes of delicate fabrics that otherwise are vulnerable to high temperatures.
引用
收藏
页码:1071 / 1079
页数:9
相关论文
共 50 条
  • [1] Purification and characterization of a cold active alkaline protease from Stenotrophomonas sp., isolated from Kashmir, India
    Iram Saba
    Parvaiz H. Qazi
    Shabir A. Rather
    Refaz A. Dar
    Qurrat A. Qadri
    Nasier Ahmad
    Sarojini Johri
    Subash C. Taneja
    Sami Shawl
    [J]. World Journal of Microbiology and Biotechnology, 2012, 28 : 1071 - 1079
  • [2] Purification and characterization of alkaline protease from a newly isolated haloalkaliphilic Bacillus sp.
    Patel, Rajesh K.
    Dodia, Mital S.
    Joshi, Rupal H.
    Singh, Satya P.
    [J]. PROCESS BIOCHEMISTRY, 2006, 41 (09) : 2002 - 2009
  • [3] Purification and characterization of an alkaline protease from Micrococcus sp. isolated from the South China Sea
    Enling Hou
    Tao Xia
    Zhaohui Zhang
    Xiangzhao Mao
    [J]. Journal of Ocean University of China, 2017, 16 : 319 - 325
  • [4] Purification and characterization of an extracellular alkaline cold-adapted serine metalo-protease from the cold tolerant bacterium, Stenotrophomonas sp. BTR88
    Nikbakhti, Reihaneh
    Shahnavaz, Bahar
    Asoodeh, Ahmad
    [J]. INDIAN JOURNAL OF BIOCHEMISTRY & BIOPHYSICS, 2021, 58 (05): : 444 - 450
  • [5] New alkaline protease from Nocardiopsis sp.:: partial purification and characterization
    Moreira, KA
    Porto, TS
    Teixeira, MFS
    Porto, ALF
    Lima, JL
    [J]. PROCESS BIOCHEMISTRY, 2003, 39 (01) : 67 - 72
  • [6] Purification and characterization of fibrinolytic alkaline protease from Fusarium sp. BLB
    Mitsuhiro Ueda
    Toshihiro Kubo
    Kazutaka Miyatake
    Takumi Nakamura
    [J]. Applied Microbiology and Biotechnology, 2007, 74 : 331 - 338
  • [7] Purification and Characterization of Alkaline Protease from Bacillus sp. HD292
    Putatunda C.
    Kundu B.S.
    Bhatia R.
    [J]. Proceedings of the National Academy of Sciences, India Section B: Biological Sciences, 2019, 89 (3) : 957 - 965
  • [8] Thermostable alkaline protease from newly isolated Vibrio sp.: extraction, purification and characterisation
    Ponnambalam Subhashini
    Neelamegam Annamalai
    Ayyappan Saravanakumar
    Thangavel Balasubramanian
    [J]. Biologia, 2012, 67 : 629 - 635
  • [9] Thermostable alkaline protease from newly isolated Vibrio sp.: extraction, purification and characterisation
    Subhashini, Ponnambalam
    Annamalai, Neelamegam
    Saravanakumar, Ayyappan
    Balasubramanian, Thangavel
    [J]. BIOLOGIA, 2012, 67 (04) : 629 - 635
  • [10] Isolation, Screening and Characterization of Cold Active Alkaline Protease from wular Lake of Kashmir Region
    Furhan, Junaid
    Sharma, Sarika
    [J]. INTERNATIONAL JOURNAL OF ADVANCED BIOTECHNOLOGY AND RESEARCH, 2014, 5 (04): : 576 - 581