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Virginia Polytechnic Institute and State University

Production, purification and properties of Bacillus thuringiensis neutral protease

Abstract

dc:description.abstract

Although the insect pathogenicity of Bacillus thuringiensis is reasonably well understood, relatively little is known about other facets of this microorganism's physiology. At the time of sporulation, the organism produces in addition to the spore and toxic paraspore (crystal) an extracellular proteolytic enzyme. This study concerns the conditions for production, the.purification and the properties of this enzyme. It was found in studies relating to production of protease that B. thuringiensis var. kurstaki (HD-1) produced a considerable quantity of the enzyme in a protease production medium (PPM). This medium contained 7 x 10⁻³ M CaCl₂, 5 x 10⁻⁴ of M MnCl₂ and 1 x 10⁻³ M MgCl₂ in nutrient broth. Manganese was required for enzyme synthesis and calcium was required for enzyme stability. Starting with a large volume of crude enzyme preparation obtained from the culture supernatant of B. thuringiensis grown in PPM, the enzyme was purified 97 x. The purification steps included Amicon ultrafiltration cell concentration, ammonium sulfate fractionation, and potato starch adsorption. Electrophoresis on SDS-polyacrylamide gels showed a single protein band at the last purification step. The enzyme had a pH optimum around pH 6.5-7.0 and was sensitive to metal chelating agents such as EDTA and O-phenanthroline. The molecular weight of the neutral protease has been estimated to be about 37,000 by electrophoresis in SDS-polyacrylamide gels. In the presence of 0.1% calcium acetate, the enzyme is quite stable at 60 C after 10 minutes incubation. It lacks esterase activity when tested against acetyl-tyrosine ethyl ester and benzoylarginine ethyl ester. All the above properties indicate the similarity of the Bacillus thuringiensis neutral protease to those produced by other members of the genus Bacillus as well as to the other microbial neutral proteases.

Degree

thesis:*
Name thesis:degree_name
Master of Science
Level thesis:degree_level
masters
Discipline thesis:degree_discipline
Microbiology
Department dc:contributor.department
Microbiology
Grantor dc:publisher
Virginia Polytechnic Institute and State University
Year dc:date.issued
1974

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Li, Eugenia Yee-Ching

Rights

dc:rights
Statement dc:rights
  • In Copyright
Language dc:language.iso
en

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/10919/70564
OAI identifier oai:identifier
oai:vtechworks.lib.vt.edu:10919/70564

Chain of custody

source
Harvested from
Virginia Tech
Base URL
vtechworks.lib.vt.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
related terms
citation

Li, Eugenia Yee-Ching. Production, purification and properties of Bacillus thuringiensis neutral protease. masters thesis, Virginia Polytechnic Institute and State University, 1974. http://hdl.handle.net/10919/70564