Differences in expression of two endoxylanase genes (xynA and xynB) from Penicillium purpurogenum

被引:37
作者
Chávez, R
Schachter, K
Navarro, C
Peirano, A
Aguirre, C
Bull, P
Eyzaguirre, J
机构
[1] Pontificia Univ Catolica Chile, Lab Bioquim, Dept Genet Mol & Microbiol, Santiago, Chile
[2] Univ Andres Bello, Escuela Artes Liberales, Santiago, Chile
关键词
glycosyl hydrolases; promoter sequences; gene expression; inverted polymerase chain reaction;
D O I
10.1016/S0378-1119(02)00720-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A number of xylanolytic microorganisms secrete to the medium several molecular forms of endoxylanases. The physiological function of these isoforms is not clears one possibility is that they are produced under different growth conditions. To study this problem, we have used two endoxylanases (XynA and XynB) produced by the fungus Penicillium purpurogenum. These enzymes have been previously purified and characterized; they belong to family 10 and 11 of the glycosyl hydrolases, respectively. The promoters of the xynA and xynB genes have been sequenced: both present consensus sequences for the binding of the carbon catabolite repressor CreA, but otherwise show substantial differences. The xynB promoter has eight boxes in tandem for the binding of the XlnR activator and lacks the consensus sequence for the PacC pH regulator. On the other hand, the xynA promoter contains one XlnR box and three PacC consensus sequences. To investigate if these differences are reflected in gene expression, Northern blot assays were carried out. The xynA gene is transiently expressed when oat spell xylan is used as carbon source, but negligible expression was observed with birchwood xylan, xylose or xylitol. In contrast, xynB is broadly induced by all these carbon sources; this may be related to the presence of several XlnR boxes. Similar results were obtained by zymogram analysis of the expressed proteins. The different induction capabilities of birchwood and oat spelt xylan may be due to differences in their composition and structure. Expression assays carried out at different pH reflects that, despite the lack of PacC binding sites in the xynB promoter, this gene is tightly regulated by pH. The findings described here illustrate new and important differences between endoxylanases from families 10 and 11 in P. purpurogenum. They may help explain the production of multiple endoxylanase forms by this organism. (C) 2002 Published by Elsevier Science B.V.
引用
收藏
页码:161 / 168
页数:8
相关论文
共 34 条
  • [1] BAINBRIDGE BW, 1990, FEMS MICROBIOL LETT, V66, P113, DOI [10.1111/j.1574-6968.1990.tb03981.x, 10.1016/0378-1097(90)90267-T]
  • [2] PENICILLIUM-PURPUROGENUM PRODUCES SEVERAL XYLANASES - PURIFICATION AND PROPERTIES OF 2 OF THE ENZYMES
    BELANCIC, A
    SCARPA, J
    PEIRANO, A
    DIAZ, R
    STEINER, J
    EYZAGUIRRE, J
    [J]. JOURNAL OF BIOTECHNOLOGY, 1995, 41 (01) : 71 - 79
  • [3] Electrophoretic karyotype of the filamentous fungus Penicillium purpurogenum and chromosomal location of several xylanolytic genes
    Chávez, R
    Fierro, F
    Gordillo, F
    Martín, JF
    Eyzaguirre, J
    [J]. FEMS MICROBIOLOGY LETTERS, 2001, 205 (02) : 379 - 383
  • [4] Chávez R, 2001, BIOL RES, V34, P217
  • [5] 2 DIFFERENT, ADJACENT AND DIVERGENT ZINC-FINGER BINDING-SITES ARE NECESSARY FOR CREA-MEDIATED CARBON CATABOLITE REPRESSION IN THE PROLINE GENE-CLUSTER OF ASPERGILLUS-NIDULANS
    CUBERO, B
    SCAZZOCCHIO, C
    [J]. EMBO JOURNAL, 1994, 13 (02) : 407 - 415
  • [6] An endo-1,4-β-xylanase-encoding gene from Agaricus bisporus is regulated by compost-specific factors
    De Groot, PWJ
    Basten, DEJW
    Sonnenberg, ASM
    Van Griensven, LJLD
    Visser, J
    Schaap, PJ
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1998, 277 (02) : 273 - 284
  • [7] An α-L-arabinofuranosidase from Penicillium purpurogenum:: production, purification and properties
    De Ioannes, P
    Peirano, A
    Steiner, J
    Eyzaguirre, J
    [J]. JOURNAL OF BIOTECHNOLOGY, 2000, 76 (2-3) : 253 - 258
  • [8] DEGRAAFF LH, 1994, MOL MICROBIOL, V12, P479
  • [9] PH regulation of gene expression in fungi
    Denison, SH
    [J]. FUNGAL GENETICS AND BIOLOGY, 2000, 29 (02) : 61 - 71
  • [10] Cloning, sequencing and expression of the cDNA of endoxylanase B from Penicillium purpurogenum
    Diaz, R
    Sapag, A
    Peirano, A
    Steiner, J
    Eyzaguirre, J
    [J]. GENE, 1997, 187 (02) : 247 - 251