The exopolygalacturonate lyase PelW and the oligogalacturonate lyase Ogl, two cytoplasmic enzymes of pectin catabolism in Erwinia chrysanthemi 3937

被引:65
作者
Shevchik, VE [1 ]
Condemine, G [1 ]
Robert-Baudouy, J [1 ]
Hugouvieux-Cotte-Pattat, N [1 ]
机构
[1] INSA, Lab Genet Mol Microorganismes & Interact Cellulai, CNRS, UMR 5577, F-69621 Villeurbanne, France
关键词
D O I
10.1128/JB.181.13.3912-3919.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Erwinia chrysanthemi 3937 secretes into the external medium several pectinolytic enzymes, among which are eight isoenzymes of the endo-cleaving pectate lyases: PelA, PelB, PelC, PelD, and PelE (family 1); PelI (family 4); Pelt (family 3); and PelZ (family 5). In addition, one exe-cleaving pectate lyase, PelX (family 3), has been found in the periplasm off. chrysanthemi. The E. chrysanthemi 3937 gene kdgC has been shown to exhibit a high degree of similarity to the genes pelY of Yersinia pseudotuberculosis and pelB of Erwinia carotovora, which encode family 2 pectate lyases. However, no pectinolytic activity has been assigned to the KdgC protein. After verification of the corresponding nucleotide sequence, we cloned a longer DNA fragment and showed that this gene encodes a 553-amino-acid protein exhibiting an exe-cleaving pectate lyase activity. Thus, the kdgC gene was renamed pelW. PelW catalyzes the formation of unsaturated digalacturonates from polygalacturonate or short oligogalacturonates. PelW is located in the bacterial cytoplasm. In this compartment, PelW action could complete the degradation of pectic oligomers that was initiated by the extracellular or periplasmic pectinases and precede the action of the cytoplasmic oligogalacturonate lyase, Ogl. Both cytoplasmic pectinases, PelW and Ogl, seem to act in sequence during oligogalacturonate depolymerization, since oligomers longer than dimers are very poor substrates for Ogl but are good substrates for PelW. The estimated number of binding subsites for PelW is three, extending from subsite -2 to +1, while it is probably two for Ogl, extending from subsite -1 to +1. The activities of the two cytoplasmic lyases, PelW and Ogl, are dependent on the presence of divalent cations, since both enzymes are inhibited by EDTA. In contrast to the extracellular pectate lyases, Ca2+ is unable to restore the activity of PelW or Ogl, while several other cations, including Co2+, Mn2+, and Ni2+, can activate both cytoplasmic lyases.
引用
收藏
页码:3912 / 3919
页数:8
相关论文
共 40 条
[1]   USE OF TN5TAC1 TO CLONE A PEL GENE ENCODING A HIGHLY ALKALINE, ASPARAGINE-RICH PECTATE LYASE ISOZYME FROM AN ERWINIA-CHRYSANTHEMI EC16 MUTANT WITH DELETIONS AFFECTING THE MAJOR PECTATE LYASE ISOZYMES [J].
ALFANO, JR ;
HAM, JH ;
COLLMER, A .
JOURNAL OF BACTERIOLOGY, 1995, 177 (15) :4553-4556
[2]   MOLECULAR-CLONING OF THE STRUCTURAL GENE FOR EXOPOLYGALACTURONATE LYASE FROM ERWINIA-CHRYSANTHEMI EC16 AND CHARACTERIZATION OF THE ENZYME PRODUCT [J].
BROOKS, AD ;
HE, SY ;
GOLD, S ;
KEEN, NT ;
COLLMER, A ;
HUTCHESON, SW .
JOURNAL OF BACTERIOLOGY, 1990, 172 (12) :6950-6958
[3]   WHO DROPS OUT OF CLINICAL-TRIALS - THE VA COOPERATIVE STUDY EXPERIENCE [J].
COLLINS, JF ;
BINGHAM, SF ;
WILLIFORD, WO ;
WEISS, DG .
CONTROLLED CLINICAL TRIALS, 1981, 2 (01) :78-78
[4]   AN EXO-POLY-ALPHA-D-GALACTURONOSIDASE IMPLICATED IN THE REGULATION OF EXTRACELLULAR PECTATE LYASE PRODUCTION IN ERWINIA-CHRYSANTHEMI [J].
COLLMER, A ;
WHALEN, CH ;
BEER, SV ;
BATEMAN, DF .
JOURNAL OF BACTERIOLOGY, 1982, 149 (02) :626-634
[5]   ANALYSIS OF AN ERWINIA-CHRYSANTHEMI GENE-CLUSTER INVOLVED IN PECTIN DEGRADATION [J].
CONDEMINE, G ;
ROBERTBAUDOUY, J .
MOLECULAR MICROBIOLOGY, 1991, 5 (09) :2191-2202
[6]  
COPELAND BR, 1982, J BIOL CHEM, V257, P5065
[7]  
GONZALEZCANDELAS L, 1992, J BACTERIOL, V174, P6343
[8]   MOLECULAR-CLONING, NUCLEOTIDE-SEQUENCE, AND MARKER EXCHANGE MUTAGENESIS OF THE EXO-POLY-ALPHA-D-GALACTURONOSIDASE-ENCODING PEHX GENE OF ERWINIA-CHRYSANTHEMI EC16 [J].
HE, SY ;
COLLMER, A .
JOURNAL OF BACTERIOLOGY, 1990, 172 (09) :4988-4995
[9]   STRUCTURE-BASED MULTIPLE ALIGNMENT OF EXTRACELLULAR PECTATE LYASE SEQUENCES [J].
HEFFRON, S ;
HENRISSAT, B ;
YODER, MD ;
LIETZKE, S ;
JURNAK, F .
MOLECULAR PLANT-MICROBE INTERACTIONS, 1995, 8 (02) :331-334
[10]   FUNCTIONAL IMPLICATIONS OF STRUCTURE-BASED SEQUENCE ALIGNMENT OF PROTEINS IN THE EXTRACELLULAR PECTATE LYASE SUPERFAMILY [J].
HENRISSAT, B ;
HEFFRON, SE ;
YODER, MD ;
LIETZKE, SE ;
JURNAK, F .
PLANT PHYSIOLOGY, 1995, 107 (03) :963-976