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1 tions, but the Pel fragment bound to calcium pectate, a major constituent of the plant cell wall.
2 , the primary sequence alignment between the pectate and pectin lyase subfamilies has been corrected
3 atively charged pectin to create an extensin pectate coacervate that may template further orderly dep
4  ordered and represent an atomic view of the pectate component in plant cell walls.
5 thogen Erwinia chrysanthemi and degrades the pectate component of plant cell walls in soft rot diseas
6 ity (anhydrouronic acid, methoxy and calcium pectate contents and degree of esterification).
7                      The conformation of the pectate fragment is a mix of 21 and 31 right-handed heli
8 he pel gene from an Amycolata sp. encoding a pectate lyase (EC 4.2.2.2) was isolated by activity scre
9 winia carotovora secrete several isozymes of pectate lyase (Pel) by the out-encoded type II pathway.
10 es showing sequence homology to higher-plant pectate lyase (Pel) genes were isolated from ripening ba
11 uppress host defense responses, and secretes pectate lyase (Pel) to degrade the plant cell wall.
12 ora subsp. carotovora produces extracellular pectate lyase (Pel), polygalacturonase (Peh), cellulase
13 tococca, a plant pathogen, has two inducible pectate lyase (PL) genes (pel) encoding PL that can help
14 erase (PME), pectin acetylesterase (PAE) and pectate lyase (PL) where all highly expressed and latex-
15 , beta-glucosidase, beta-amylase, chitinase, pectate lyase (PL), pectinesterase (PE) and polygalactur
16 hat the production of extracellular enzymes (pectate lyase [Pel], polygalacturonase [Peh], cellulase
17 we report a gene for a cellulosomal subunit, pectate lyase A (PelA), lying downstream of the engY gen
18  a significant increase in calcium-dependent pectate lyase activity during ripening.
19 el gene in S. lividans TK24 resulted in high pectate lyase activity in the culture supernatant, conco
20                                              Pectate lyase activity is detected in elongating and dif
21                                           No pectate lyase activity was detected in E. coli BL21 with
22                                  Although no pectate lyase activity was detected, the C-terminal regi
23               The purified LjNPL protein had pectate lyase activity, demonstrating that this activity
24 el clone produced a recombinant protein with pectate lyase activity, demonstrating that this sequence
25 Escherichia coli possesses calcium-dependent pectate lyase activity.
26           Homogalacturonan solubilization by pectate lyase and calcium chelation greatly increased th
27 e show that two pectin modification genes, a pectate lyase and pectinesterase, are targets of both bH
28                     The folding mechanism of pectate lyase C (pelC) involves two slow phases that hav
29                                              Pectate lyase C (pelC) is a member of the class of prote
30 mensional structure of a complex between the pectate lyase C (PelC) R218K mutant and a plant cell wal
31                                              Pectate lyase C (pelC) was the first protein in which th
32 n with the structure of Erwinia chrysanthemi pectate lyase C (PelC), the primary sequence alignment b
33 or in vitro activity of Erwinia chrysanthemi pectate lyase C (PelC).
34                        When modeled based on pectate lyase C of Erwinia chrysanthemi, the RHbetaH of
35 he first avirulence gene and determined that pectate lyase C possessed a novel structural motif, know
36                                The Amycolata pectate lyase clearly belongs to the pectate lyase super
37                                The Amycolata pectate lyase contains a signal peptide of 26 amino acid
38 ase family, in contrast to that found in the pectate lyase enzymes.
39                             High xylanase or pectate lyase expression was observed when C. cellulovor
40  precise signals controlling the dynamics of pectate lyase expression were unclear.
41 uronate lyases (OGLs; now also classified as pectate lyase family 22) are cytoplasmic enzymes found i
42 e invariant and conserved amino acids in the pectate lyase family of proteins.
43 bserved between the cellular distribution of pectate lyase folding and the distinct metal coordinatio
44 harpins have C-terminal enzyme-like domains: pectate lyase for HopAK1 and lytic transglycosylase for
45  with PelE from Erwinia chrysanthemi and the pectate lyase from Glomerella cingulata.
46                                              Pectate lyase from Paenibacillus lactis PKC5 had Km and
47 inal amino-acid sequence match the wild-type pectate lyase from the Amycolata sp.
48 ere we identify a Lotus japonicus nodulation pectate lyase gene (LjNPL), which is induced in roots an
49 ce in pmr6, a mutant defective in a putative pectate lyase gene.
50 re have been no reports available to date on pectate lyase genes from Clostridia.
51 orial extracts and high expression levels of pectate lyase genes suggest that the parasite contribute
52                                              Pectate lyase is a hydrolytic enzyme used by diverse ind
53 cc71) produces extracellular enzymes such as pectate lyase isozymes (Pels), cellulase (Cel), polygala
54  the expression of the pectin-modifying gene PECTATE LYASE LIKE12 (PLL12) is required for normal stom
55 mutants displayed a significant reduction in pectate lyase production, a virulence factor of this bac
56 ng that this sequence was likely to encode a pectate lyase protein in planta.
57 l reactive arginine, analogous to the pectin/pectate lyase reaction site, is accessible to the solven
58                         In contrast, PelE, a pectate lyase secreted via the type II protein secretion
59  that an arginine, which is invariant in the pectate lyase superfamily, is the amino acid that initia
60 ycolata pectate lyase clearly belongs to the pectate lyase superfamily, sharing all functional amino
61 hlI (gene for AHL synthase), pel-1 (gene for pectate lyase), or rsmB (gene for regulatory RNA that bi
62 alin A), and parallel beta-helical proteins (pectate lyase).
63         One of these cDNAs shows homology to pectate lyase, a pectin-degrading enzyme.
64 ) for the bHLH transcription factors and the pectate lyase, but not for the pectinesterase, complemen
65 gh levels of the exoenzyme virulence factors pectate lyase, cellulase and protease.
66 ta-helix as seen in the pectinolytic enzymes pectate lyase, pectin lyase, polygalacturonase and rhamn
67            The basal levels of extracellular pectate lyase, polygalacturonase, and cellulase as well
68  FlhDC(-) mutant produces very low levels of pectate lyase, polygalacturonase, cellulase, protease, a
69                       During incubation with pectate lyase, the clarity percentage of the grape juice
70 rate-binding clefts of polygalacturonase and pectate lyase, which bind and cleave the same substrate,
71                  Reverse genetics identified PECTATE LYASE-LIKE 12 (PLL12) as critical for plant grow
72 e in a glycosylphosphatidylinositol-anchored pectate lyase-like gene) exhibited a strong increase in
73 a previously described member of a family of pectate lyase-like genes.
74                               PMR6 encodes a pectate lyase-like protein with a novel C-terminal domai
75 re we report direct interaction of NPG1 with pectate lyase-like proteins (PLLs).
76      The present experiment aimed to isolate pectate lyase-producing bacteria that can tolerate an al
77  comparison of the efficiency of eight other pectate lyase-producing microorganisms with that of D. d
78  of ripening, by silencing a gene encoding a pectate lyase.
79 e active site and substrate-binding cleft of pectate lyase.
80 combined activities of polygalacturonase and pectate lyase.
81  PKC5, and Bacillus sonorensis ADCN produced pectate lyase.
82 ruit firmness, with the notable exception of pectate lyase.
83 ough the action of pectin-methylesterase and pectate-lyase that possibly originated from a microbial
84 nd Erwinia carotovora secrete extra-cellular pectate lyases (Pels) using the type II or Out pathway.
85  protein with domains resembling harpins and pectate lyases (Pels), respectively.
86 inding, and cell wall modification including pectate lyases and expansins.
87 nearly identical to that found in the pectin/pectate lyases from several plant pathogenic microorgani
88 lished and new information about the role of pectate lyases in plant development forms the focus of t
89                                  The role of pectate lyases in plant development has received little
90 imely expression of pel genes encoding major pectate lyases is essential to circumvent the plant defe
91 e C-terminal region of HrpW is homologous to pectate lyases of a unique class, suggesting that HrpW m
92                     However, the orthologous pectate lyases Pel3 and PelI from these bacteria, which
93                                Thanks to the pectate lyases produced by bacteria cultivated in the ve
94 l DNA libraries more than 40 novel microbial pectate lyases were discovered, and their enzymatic prop
95 rwinia chrysanthemi belonging to family 1 of pectate lyases, a putative cellulose-binding domain, a c
96  E. chrysanthemi that belongs to family 4 of pectate lyases, and a duplicated sequence (or dockerin)
97 xpressed in mature pollen, shows homology to pectate lyases, and is the putative homologue of the tom
98 e distinct metal coordination chemistries of pectate lyases.
99 ructure and function of Erwinia chrysanthemi pectate lysase C, a plant virulence factor, is reviewed