Cloning and disruption of the antigenic catalase gene of Aspergillus fumigatus

被引:103
作者
Calera, JA
Paris, S
Monod, M
Hamilton, AJ
Debeaupuis, JP
Diaquin, M
LopezMedrano, R
Leal, F
Latge, JP
机构
[1] INST PASTEUR, LAB ASPERGILLUS, F-75724 PARIS 15, FRANCE
[2] CHU VAUDOIS, SERV DERMATOL, CH-1011 LAUSANNE, SWITZERLAND
[3] GUYS HOSP, DERMATOL LAB, LONDON SE1 9RT, ENGLAND
[4] UNIV SALAMANCA, DEPT GENET & MICROBIOL, E-37008 SALAMANCA, SPAIN
关键词
D O I
10.1128/IAI.65.11.4718-4724.1997
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aspergillus fumigatus possesses two catalases (described as fast and slow on the basis of their electrophoretic mobility). The slow catalase has been recognized as a diagnostic antigen for aspergillosis in immunocompetent patients. The antigenic catalase has been purified. The enzyme is a tetrameric protein composed of 90-kDa subunits. The corresponding cat1 gene was cloned, and sequencing data show that the cat1 gene codes for a 728-amino-acid polypeptide. A recombinant protein expressed in Pichia pastoris is enzymatically active and has biochemical and antigenic properties that are similar to those of the wild-type catalase. Molecular experiments reveal that CAT1 contains a signal peptide and a propeptide of 15 and 12 amino acrid residues, respectively. cat1-disrupted mutants that were unable to produce the slow catalase were as sensitive to H2O2 and polymorphonuclear cells as the wild-type strain. In addition, there was no difference in pathogenicity between the cat1 mutant and its parental cat1(+) strain in a murine model of aspergillosis.
引用
收藏
页码:4718 / 4724
页数:7
相关论文
共 49 条
  • [1] ASPERGILLUS-FUMIGATUS ALLERGEN-I, A MAJOR IGE-BINDING PROTEIN, IS A MEMBER OF THE MITOGILLIN FAMILY OF CYTOTOXINS
    ARRUDA, LK
    PLATTSMILLS, TAE
    FOX, JW
    CHAPMAN, MD
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (05) : 1529 - 1532
  • [2] Biochemical and antigenic characterization of a new dipeptidyl-peptidase isolated from Aspergillus fumigatus
    Beauvais, A
    Monod, M
    Debeaupuis, JP
    Diaquin, M
    Kobayashi, H
    Latge, JP
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (10) : 6238 - 6244
  • [3] HETEROLOGOUS GENE-EXPRESSION BY FILAMENTOUS FUNGI - SECRETION OF HUMAN INTERLEUKIN-6 BY ASPERGILLUS-NIDULANS
    CARREZ, D
    JANSSENS, W
    DEGRAVE, P
    VANDENHONDEL, CAMJJ
    KINGHORN, JR
    FIERS, W
    CONTRERAS, R
    [J]. GENE, 1990, 94 (02) : 147 - 154
  • [4] DEBEAUPUIS JP, 1995, CAN J BOT, V73, pS1087
  • [5] THE ACTIVE-CENTER OF CATALASE
    FITA, I
    ROSSMANN, MG
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1985, 185 (01) : 21 - 37
  • [6] Purification and characterization of an endo-1,3-beta-glucanase from Aspergillus fumigatus
    Fontaine, T
    Hartland, RP
    Beauvais, A
    Diaquin, M
    Latge, JP
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 243 (1-2): : 315 - 321
  • [7] THE CATR GENE ENCODING A CATALASE FROM ASPERGILLUS-NIGER - PRIMARY STRUCTURE AND ELEVATED EXPRESSION THROUGH INCREASED GENE COPY NUMBER AND USE OF A STRONG PROMOTER
    FOWLER, T
    REY, MW
    VAHAVAHE, P
    POWER, SD
    BERKA, RM
    [J]. MOLECULAR MICROBIOLOGY, 1993, 9 (05) : 989 - 998
  • [8] YEAST PROHORMONE PROCESSING ENZYME (KEX2 GENE-PRODUCT) IS A CA-2+-DEPENDENT SERINE PROTEASE
    FULLER, RS
    BRAKE, A
    THORNER, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (05) : 1434 - 1438
  • [9] SEQUENCE DIFFERENCES BETWEEN GLYCOSYLATED AND NONGLYCOSYLATED ASN-X-THR SER ACCEPTOR SITES - IMPLICATIONS FOR PROTEIN ENGINEERING
    GAVEL, Y
    VONHEIJNE, G
    [J]. PROTEIN ENGINEERING, 1990, 3 (05): : 433 - 442
  • [10] DEVELOPMENT OF DNA PROBES FOR FINGERPRINTING ASPERGILLUS-FUMIGATUS
    GIRARDIN, H
    LATGE, JP
    SRIKANTHA, T
    MORROW, B
    SOLL, DR
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (06) : 1547 - 1554