ライフサイエンスコーパス: Erwinia chrysanthemi

1 se produced by Escherichia coli (ASNase) and Erwinia chrysanthemi.

2 the GH 5 endoxylanase secreted by strains of Erwinia chrysanthemi.

3 rticular the cbr locus of the plant pathogen Erwinia chrysanthemi.

4 carried on cosmid pCPP2156, was cloned from Erwinia chrysanthemi, a pathogen that differs from P. sy

5 trates in the enzymatic activity of PME from Erwinia chrysanthemi, a processive enzyme that catalyzes

6 ously reported homologous enzyme, XynA, from Erwinia chrysanthemi and analyzes the ligand binding sit

7 s a similar structural topology as Pels from Erwinia chrysanthemi and Bacillus subtilis.

8 pe II systems from Klebsiella oxytoca (pul), Erwinia chrysanthemi and carotovora (out), Xanthomonas c

9 PelC is secreted by the plant pathogen Erwinia chrysanthemi and degrades the pectate component

10 The plant pathogens Erwinia chrysanthemi and Erwinia carotovora secrete extr

11 The plant pathogens Erwinia chrysanthemi and Erwinia carotovora secrete seve

12 to genes encoding protease export systems in Erwinia chrysanthemi and Pseudomonas aeruginosa.

13 sequence showed 40% identity with PelE from Erwinia chrysanthemi and the pectate lyase from Glomerel

14 om Nectria haematococca, Erwinia carotovora, Erwinia chrysanthemi, and Bacillus subtilis, and a purif

15 Erwinia chrysanthemi ASNase (Erwinia) substitution was a

16 ally homologous to the C terminus of PelB of Erwinia chrysanthemi belonging to family 1 of pectate ly

17 We found that ELIC, a pLGIC from Erwinia chrysanthemi, can be functionally inhibited by i

18 We report that the type III machinery of Erwinia chrysanthemi cloned in Escherichia coli recogniz

19 1,4-xylan hydrolase (xylanase A) produced by Erwinia chrysanthemi D1 isolated from corn was analyzed

20 The Erwinia chrysanthemi dsbC gene was identified in a previ

21 ations were introduced into the pelC gene of Erwinia chrysanthemi EC16 that directed single or double

22 ng gene tolC in the bacterial plant pathogen Erwinia chrysanthemi EC16.

23 erichia coli B, Klebsiella oxytoca M5A1, and Erwinia chrysanthemi EC16.

24 n of exoenzymes), is a close relative of the Erwinia chrysanthemi (Echr) gene pecT and encodes a memb

25 rystal structure of a bacterial homolog from Erwinia chrysanthemi (ELIC) agrees with previous structu

26 The ligand-gated ion channel from Erwinia chrysanthemi (ELIC) is a prokaryotic homolog of

27 annels from Gloeobacter violaceus (GLIC) and Erwinia chrysanthemi (ELIC), whose crystal structures ar

28 The structure of the Erwinia chrysanthemi enzyme was solved by multiple isomo

29 specificity and the processive action of the Erwinia chrysanthemi enzyme.

30 Both the Escherichia coli (EcAII) and Erwinia chrysanthemi (ErAII) type II ASNases currently u

31 C 3.2.1.8) from the bacterial plant pathogen Erwinia chrysanthemi expressed in Escherichia coli, a 45

32 Genes homologous to Escherichia coli and Erwinia chrysanthemi glucuronate and galacturonate metab

33 mensional structure of shikimate kinase from Erwinia chrysanthemi has been determined by multiple iso

34 the pentameric ligand-gated ion channel from Erwinia chrysanthemi, is a prototype for Cys-loop recept

35 ted our recently described structures of the Erwinia chrysanthemi l-asparaginase (ErA) to inform the

36 ution crystal structures of the complexes of Erwinia chrysanthemi L-asparaginase (ErA) with the produ

37 we report the x-ray crystal structure of the Erwinia chrysanthemi ligand-gated ion channel (ELIC) in

38 ptors, ion channels from prokaryote homologs-Erwinia chrysanthemi ligand-gated ion channel (ELIC), Gl

39 ly reported for the prokaryotic homolog, the Erwinia chrysanthemi ligand-gated ion channel (ELIC).

40 conserved in homomeric GABA(A)Rs and in the Erwinia chrysanthemi ligand-gated ion channel and may be

41 n suggested that the bacterial homolog ELIC (Erwinia chrysanthemi ligand-gated ion channel) has a sim

42 m, and negatively regulated by HexA (PecT in Erwinia chrysanthemi; LrhA [LysR homolog A] in Escherich

43 By comparison with the structure of Erwinia chrysanthemi pectate lyase C (PelC), the primary

44 Ca(2+) is essential for in vitro activity of Erwinia chrysanthemi pectate lyase C (PelC).

45 The structure and function of Erwinia chrysanthemi pectate lysase C, a plant virulence

46 Erwinia chrysanthemi produces a battery of hydrolases an

47 w that l-ases from both Escherichia coli and Erwinia chrysanthemi profoundly inhibit mTORC1 and prote

48 (typified by Escherichia coli HlyBD/TolC or Erwinia chrysanthemi PrtDEF) that utilize C-terminal sec

49 ae, Burkholderia glumae, Xanthomonas oryzae, Erwinia chrysanthemi, Pseudomonas syringae, and Acidovor

50 efficacy and safety of JZP458 (asparaginase erwinia chrysanthemi [recombinant]-rywn), a recombinant

51 al structure of MtSK (this work) and that of Erwinia chrysanthemi SK suggest a concerted conformation

52 te in a community annotation project for the Erwinia chrysanthemi strain 3937 genome.

53 elicitor harpin (HrpN) of soft rot pathogen Erwinia chrysanthemi strains 3937 and EC16 is secreted v

54 When modeled based on pectate lyase C of Erwinia chrysanthemi, the RHbetaH of AlgG has a long sha

55 Here, we demonstrate that Erwinia chrysanthemi, which does not carry curli genes,

56 resembles that of pehX, an exo-PG gene from Erwinia chrysanthemi, with 47.2% identity at the amino a

57 mophilus influenzae, Pseudomonas aeruginosa, Erwinia chrysanthemi, Yersinia pseudotuberculosis, Vibri