Neutral protease useful for animal tissue and cell culture
First Claim
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1. A neutral protease having the following characteristics:
- a. optimum pH of 8.5 for proteolytic activity to casein,b. stable within a pH range of 4-9,c. active within a temperature range of 20°
-75°
C, with the optimum temperature being 60°
C,d. absence of activity at pH below 3 and pH above 10, and absence of activity upon heating at 65°
C for 10 minutes,e. activity inhibited by ethylene-diaminetetraacetate, citric acid, o-phenanthroline, 2,2'"'"'-dipyridyl, sodium fluoride, N-bromosuccinimide and iodine,f. activity enhanced by Ca++, Mn++, Mg++, Fe++, Fe+++ and Al+++,g. molecular weight of 35,900 as determined by ultracentrifugal analysis,h. elemental analysis of 46.57% C, 7.17% H, 31.57% O, 14.48% N and 0.21% S, andi. cleaves the peptide bonds in the oxidized B-chain of insulin at positions Phe(1)-Val(2), His(5)-Leu(6), His(10)-Leu(11), Glu(13)-Ala(14), Ala(14)-Leu(15), Leu(15)-Tyr(16), Tyr(16)-Leu(17), Leu(17)-Val(18), Gly(23)-Phe(24), Phe(24)-Phe(25), Phe(25)-Tyr(26) and Lys(29)-Ala(30).
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Abstract
This invention relates to a neutral protease useful for animal tissue cell culture and having the chemical and physical properties disclosed in the body of the specification, characterized in that said protease is produced by aerobically culturing a strain of Bacillus polymyxa deposited at the American Type Culture Collection, Rockville, Maryland under accession number ATCC 21993 on a culture medium containing a suitable carbon source and nitrogen source.
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1 Claim
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1. A neutral protease having the following characteristics:
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a. optimum pH of 8.5 for proteolytic activity to casein, b. stable within a pH range of 4-9, c. active within a temperature range of 20°
-75°
C, with the optimum temperature being 60°
C,d. absence of activity at pH below 3 and pH above 10, and absence of activity upon heating at 65°
C for 10 minutes,e. activity inhibited by ethylene-diaminetetraacetate, citric acid, o-phenanthroline, 2,2'"'"'-dipyridyl, sodium fluoride, N-bromosuccinimide and iodine, f. activity enhanced by Ca++, Mn++, Mg++, Fe++, Fe+++ and Al+++, g. molecular weight of 35,900 as determined by ultracentrifugal analysis, h. elemental analysis of 46.57% C, 7.17% H, 31.57% O, 14.48% N and 0.21% S, and i. cleaves the peptide bonds in the oxidized B-chain of insulin at positions Phe(1)-Val(2), His(5)-Leu(6), His(10)-Leu(11), Glu(13)-Ala(14), Ala(14)-Leu(15), Leu(15)-Tyr(16), Tyr(16)-Leu(17), Leu(17)-Val(18), Gly(23)-Phe(24), Phe(24)-Phe(25), Phe(25)-Tyr(26) and Lys(29)-Ala(30).
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Specification