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