Cloning and expression of the complement fixation antigen-chitinase of Coccidioides immitis

29Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

A chitinase had been isolated from the culture filtrates of Coccidioides immitis endosporulating spherules and from hyphae and shown to be the coccidioidal complement fixation (CF) and immunodiffusion-CF antigen. In the present study, we made use of our previously determined amino-terminal (N- terminal) sequence of the CF-chitinase to design degenerate oligonucleotide primers and to amplify and sequence a PCR product that coded for the N- terminal portion of the CF-chitinase. The PCR product was used as a hybridization probe to screen a developing spherule-λZAP cDNA library, and three hybridizing clones were selected. These clones were converted into their pBluescript expression plasmid form in Escherichia coli and induced to express their recombinant proteins. Lysate from only one clone, pCTS 4-2A, yielded an enzymatically functional CF-chitinase and a line of identity with control immunodiffusion-CF-positive antigen. The pCTS 4-2A insert was sequenced and found to contain a deduced open reading frame coding for a 427- amino-acid polypeptide with an approximate molecular weight of 47 kDa. When purified by a chitin adsorption-desorption method, the recombinant protein exhibited virtually identical characteristics to those of the original C. immitis CF-chitinase. Nondenaturing gels of the pCTS 4-2A E. coli lysates and the purified C. immitis and recombinant CF-chitinase revealed proteins that had chitinase activity and similar relative electrophoretic mobilities. The appearance and relative levels of hybridizing RNA from the developing spherules-endospores (SEs) and hyphae correlated with the appearance or presence and level of CF-chitinase enzyme activity found in SEs culture filtrate and in cellular extracts of developing SE and hyphae. Thus, a functional recombinant CF-chitinase antigen was produced in E. coli and was used in serological diagnostic applications. These results also suggest a functional role for this chitinase in SE development and maturation.

References Powered by Scopus

Enzymatic amplification of β-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

7504Citations
N/AReaders
Get full text

A new method for predicting signal sequence cleavage sites

4113Citations
N/AReaders
Get full text

Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

4041Citations
N/AReaders
Get full text

Cited by Powered by Scopus

Review of fungal chitinases

279Citations
N/AReaders
Get full text

Defining virulence genes in the dimorphic fungi

106Citations
N/AReaders
Get full text

EST analysis of cDNA libraries from the entomopathogenic fungus Beauveria (Cordyceps) bassiana. II. Fungal cells sporulating on chitin and producing oosporein

68Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Roger Zimmermann, C., Johnson, S. M., Martens, G. W., White, A. G., & Pappagianis, D. (1996). Cloning and expression of the complement fixation antigen-chitinase of Coccidioides immitis. Infection and Immunity, 64(12), 4967–4975. https://doi.org/10.1128/iai.64.12.4967-4975.1996

Readers' Seniority

Tooltip

Professor / Associate Prof. 2

40%

Researcher 2

40%

PhD / Post grad / Masters / Doc 1

20%

Readers' Discipline

Tooltip

Immunology and Microbiology 3

50%

Medicine and Dentistry 2

33%

Biochemistry, Genetics and Molecular Bi... 1

17%

Save time finding and organizing research with Mendeley

Sign up for free