Methods of recombinantly producing neutral protease originating from paenibacillus polymyxa

Abstract

The present disclosure provides the sequence of a Paenibacillus polymyxa preproenzyme which is the precursor of a neutral protease, expression thereof in a transformed host organism, and methods for production of the neutral protease, by recombinant means. Further, use of the recombinantly produced neutral protease is disclosed in the field of cell biology, particularly for the purpose of tissue dissociation. The disclosure also includes blends with other proteases. Further disclosed are nucleotide sequences encoding the neutral protease.

1 . A method for recombinantly producing a neutral protease, the method comprising the steps of
 (a) providing in an expression vector a DNA with a sequence encoding a preproenzyme according to SEQ ID NO:5, and transforming a host organism of the species  Bacillus amyloliquefaciens  with the expression vector, thereby obtaining a transformed host organism;   (b) expressing the DNA in the transformed host organism, wherein the transformed host organism secretes the neutral protease; and   (c) isolating the secreted neutral protease;   thereby recombinantly producing the neutral protease.   
     
     
         2 . The method according to  claim 1 , wherein the DNA comprises the sequence of position 34 to position 1896 of SEQ ID NO:6. 
     
     
         3 . The method according to  claim 1 , wherein step (b) comprises culturing the transformed host organism in a liquid medium, wherein the transformed host organism secretes the neutral protease into the liquid medium. 
     
     
         4 . The method according to  claim 3 , wherein step (c) comprises isolating the secreted neutral protease from the liquid medium. 
     
     
         5 . The method according to  claim 1 , wherein the host organism is deficient of an extracellular protease selected from Npr and Apr.