Expression, purification, and molecular characterization of a full-length thermostable alkaline protease gene from Bacillus subtilis DMA-09

Biologia ◽  
2020 ◽  
Author(s):  
Dilara Abbas Bukhari ◽  
Amina Barkat ◽  
Abdul Rehman
2001 ◽  
Vol 183 (15) ◽  
pp. 4648-4651 ◽  
Author(s):  
Michihiro Hata ◽  
Mitsuo Ogura ◽  
Teruo Tanaka

ABSTRACT Expression of Bacillus subtilis aprE, encoding an extracellular alkaline protease, is positively regulated by phosphorylated DegU, the regulator of a two-component regulatory system, DegS-DegU. We found that the expression of anaprE′-′lacZ fusion was greatly reduced in a disruption mutant with a mutation of relA, which encodes the stringent factor RelA. The level of DegU in the relA mutant was similar to that in the wild-type cell. A relA degU double mutation did not result in a further decrease of theaprE′-′lacZ level found in a degU single mutant. The expression of the aprE′-′lacZ fusion in therelA mutant was stimulated by multicopy degR or the degU32(Hy) and degS200(Hy) mutations that cause the stabilization of phosphorylated DegU. Furthermore, the expression of sacB′-′lacZ, which is also dependent on phosphorylated DegU, was stimulated by the relA mutation, and this stimulation was not seen in the relA degU double mutant. These results show that RelA (or its product guanosine-3′,5′-bisdiphosphate [pp Gpp]) does not affect the phosphorylation of DegU and suggest that it participates in the expression of aprE and sacB through the regulation of DegU-dependent transcription.


2020 ◽  
Vol 8 (2) ◽  
pp. 154-160
Author(s):  
N.G. Ramesh Babu ◽  
Anupa Mary Aji

  Alkaline protease enzymes are enzymes which can catalyze the process of proteolysis between the pH ranges from 8 to 12.  Extracellular alkaline proteases are used as additives in detergent powders. In the present study, source of the organism was from a detergent contaminated area. The study has been carried out in Aeromonas hydrophila AH10 strain that produces protease enzyme with an alkaline pH optimum. The organism was a gram-negative rod with a protease enzyme activity of 0.385 ml/min. purification of the protease enzyme from the bacteria was carried out. This protease is suitable for use in alkaline detergent powders as well as in silver recovery process. The Aeromonas hydrophila strain AH10 gene encoding this high-alkaline protease was cloned and characterized.   Int. J. Appl. Sci. Biotechnol. Vol 8(2): 154-160


1991 ◽  
Vol 55 (11) ◽  
pp. 2807-2811 ◽  
Author(s):  
Kohji Murakami ◽  
Yutaka Ishida ◽  
Atsushi Masaki ◽  
Hiroki Tatsumi ◽  
Seiji Murakami ◽  
...  

1991 ◽  
Vol 55 (11) ◽  
pp. 2807-2811 ◽  
Author(s):  
Kohji MURAKAMI ◽  
Yutaka ISHIDA ◽  
Atsushi MASAKI ◽  
Hiroki TATSUMI ◽  
Seiji MURAKAMI ◽  
...  

2014 ◽  
Vol 55 (2) ◽  
pp. 160-171 ◽  
Author(s):  
Irfana Iqbal ◽  
Muhammad Nauman Aftab ◽  
Mohammed Afzal ◽  
Asad Ur-Rehman ◽  
Saima Aftab ◽  
...  

2003 ◽  
Vol 64 (10) ◽  
pp. S164
Author(s):  
Nanine de Groot ◽  
Gaby G.M. Doxiadis ◽  
Natasja G. de Groot ◽  
Nel Otting ◽  
Corrine M.C. Heijmans ◽  
...  

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