Javascript must be enabled to continue!
Proteinase Production by a Species of Cephalosporium
View through CrossRef
An unidentified
Cephalosporium
species produced an extracellular proteinase when grown in a variety of fermentation media under submerged culture conditions. Maximal enzyme yields were obtained in a medium containing 2% corn meal, 1% soybean meal, and 0.5% CaCO
3
in tap water. Optimal proteinase production in this medium occurred within a 72- to 96-hr growth period. High enzyme yields were also attained with media in which cottonseed meal, Fermatein, Pharmamedia, or soybean-α-protein was substituted for the soybean meal. The substitution of these ingredients for the corn meal resulted in significantly decreased proteinase yields. The addition of minerals or vitamins to the corn meal-soybean meal fermentation medium failed to enhance proteinase production. The enzyme was most active in an alkaline environment; maximal caseinolysis occurred at
p
H 7.5, whereas
p
H 8.5 was optimal for either hemoglobin or β-lactoglobulin hydrolysis. Enzymatic activity was also noted with either bovine albumin fraction V or soybean-α-protein substrates, whereas ovalbumin was not susceptible to enzymatic attack. The enzyme was stable within the
p
H range of 3.0 to 9.5 at 25 C for 2 hr, and at 5 C for 24 hr. The proteinase was stable upon heating for 10 min at 35 to 45 C, but it was totally inactivated at 70 C. The proteinase was unaffected by soybean inhibitor, partially inactivated by lima bean inhibitor, and completely inactivated by ovomucoid inhibitor.
Title: Proteinase Production by a Species of
Cephalosporium
Description:
An unidentified
Cephalosporium
species produced an extracellular proteinase when grown in a variety of fermentation media under submerged culture conditions.
Maximal enzyme yields were obtained in a medium containing 2% corn meal, 1% soybean meal, and 0.
5% CaCO
3
in tap water.
Optimal proteinase production in this medium occurred within a 72- to 96-hr growth period.
High enzyme yields were also attained with media in which cottonseed meal, Fermatein, Pharmamedia, or soybean-α-protein was substituted for the soybean meal.
The substitution of these ingredients for the corn meal resulted in significantly decreased proteinase yields.
The addition of minerals or vitamins to the corn meal-soybean meal fermentation medium failed to enhance proteinase production.
The enzyme was most active in an alkaline environment; maximal caseinolysis occurred at
p
H 7.
5, whereas
p
H 8.
5 was optimal for either hemoglobin or β-lactoglobulin hydrolysis.
Enzymatic activity was also noted with either bovine albumin fraction V or soybean-α-protein substrates, whereas ovalbumin was not susceptible to enzymatic attack.
The enzyme was stable within the
p
H range of 3.
0 to 9.
5 at 25 C for 2 hr, and at 5 C for 24 hr.
The proteinase was stable upon heating for 10 min at 35 to 45 C, but it was totally inactivated at 70 C.
The proteinase was unaffected by soybean inhibitor, partially inactivated by lima bean inhibitor, and completely inactivated by ovomucoid inhibitor.
Related Results
PROPERTIES OF PROTEINASE FROMSTREPTOCOCCUS FAECALISVAR.LIQUEFACIENS
PROPERTIES OF PROTEINASE FROMSTREPTOCOCCUS FAECALISVAR.LIQUEFACIENS
Bleiweis, ArnoldS. (The Pennsylvania State University, University Park),and Leonard N. Zimmerman. Properties of proteinase fromStreptococcus faecalisvar.liquefaciens. J. Bacteriol....
Impacts of man-made structures on marine biodiversity and species status - native & non-native species
Impacts of man-made structures on marine biodiversity and species status - native & non-native species
<p>Coastal environments are exposed to anthropogenic activities such as frequent marine traffic and restructuring, i.e., addition, removal or replacing with man-made structur...
Section-level genome sequencing and comparative genomics of Aspergillus sections Cavernicolus and Usti
Section-level genome sequencing and comparative genomics of Aspergillus sections Cavernicolus and Usti
Fig. S1. A cladogram representation of the phylogenetic relations between the species in this paper. The red labels show bootstrap values of 100 % and the black labels show bootstr...
A novel subtilase from common bean leaves
A novel subtilase from common bean leaves
We describe the isolation of a protease from common bean leaves grown in the field. On the basis of its biochemical properties it was classified as serine proteinase belonging to t...
Lysosomal elastase and cathepsin G in beige mice. Neutrophils of beige (Chediak-Higashi) mice selectively lack lysosomal elastase and cathepsin G.
Lysosomal elastase and cathepsin G in beige mice. Neutrophils of beige (Chediak-Higashi) mice selectively lack lysosomal elastase and cathepsin G.
A profound decrease in activities of the two lysosomal serine proteinases, elastase, and cathepsin G, was found in neutrophils of four independent beige mutants. Elastase and cathe...
The structural puzzle of how serpin serine proteinase inhibitors work
The structural puzzle of how serpin serine proteinase inhibitors work
AbstractSerine proteinase cleavage of proteins is essential to a wide variety of biological processes and is primarily regulated by protein inhibitors. Many inhibitors are conforma...
The Importance of Social Interactions and Habitat in Competition Between Microtus Agrestis and M. Arvalis
The Importance of Social Interactions and Habitat in Competition Between Microtus Agrestis and M. Arvalis
Abstract1. Microtus agrestis and M. arvalis are two very similar rodents with widely overlapping geographical ranges. One expects strong competition between them. The aim was to st...
Relationship between Fruiting Phenology and Climatic Factors in Lower Montane Forest at Doi Suthep – Pui National Park, Chiang Mai Province
Relationship between Fruiting Phenology and Climatic Factors in Lower Montane Forest at Doi Suthep – Pui National Park, Chiang Mai Province
Background and Objectives: The fruiting phenology of tree species is closely linked to seasonal patterns and climatic factors, both of which play a crucial role in determining the ...

