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1 aft poly-L-lysines on Micrococcus luteus and Erwinia carotovora.
2  plant cell wall by the pathogenic bacterium Erwinia carotovora.
3 condary metabolites are regulated by rsmA in Erwinia carotovora.
4 ous observations on the homologous system in Erwinia carotovora.
5 onsible for production of this carbapenem in Erwinia carotovora.
6        AHL controls exoprotein production in Erwinia carotovora and consequently the virulence for pl
7 applied to the study of interactions between Erwinia carotovora and different generations of dendrigr
8 t SgrS homologs from Salmonella typhimurium, Erwinia carotovora and Klebsiella pneumoniae rescue E. c
9  coli yaeT to enable Stx phage adsorption to Erwinia carotovora and the phage adsorption patterns of
10  family 5 glycosyl hydrolases from Bacillus, Erwinia carotovora, and C. acetobutylicum species.
11  Klebsiella pneumoniae, Serratia marcescens, Erwinia carotovora, and Proteus vulgaris but not in seve
12  Klebsiella pneumoniae, Serratia marcescens, Erwinia carotovora, and Proteus vulgaris, strongly sugge
13 cteria, including Pseudomonas aeruginosa and Erwinia carotovora, both significant pathogens.
14 cal genes, and genes potentially encoding an Erwinia carotovora carotovoricin Er-like bacteriocin.
15 sis of the pigment in the heterologous host, Erwinia carotovora, demonstrating, for the first time, t
16 s similar to Pels from Nectria haematococca, Erwinia carotovora, Erwinia chrysanthemi, and Bacillus s
17                 In the gamma-proteobacterium Erwinia carotovora, genes common to phosphonate biosynth
18 Strain GS101 of the bacterial phytopathogen, Erwinia carotovora, makes the simple beta-lactam antibio
19                                              Erwinia carotovora produces the beta-lactam antibiotic,
20 grobacterium tumefaciens, Pantoea stewartii, Erwinia carotovora, Ralstonia solanacearum, Pseudomonas
21 The plant pathogens Erwinia chrysanthemi and Erwinia carotovora secrete extra-cellular pectate lyases
22 The plant pathogens Erwinia chrysanthemi and Erwinia carotovora secrete several isozymes of pectate l
23          In the Gram-negative phytopathogen, Erwinia carotovora ssp. atroseptica (Eca) virulence depe
24 rotovora (Ecc) and virulence and motility in Erwinia carotovora ssp. atroseptica (Eca).
25 lence factor synthesis in the plant pathogen Erwinia carotovora ssp. carotovora (Ecc) and virulence a
26 rratia sp. ATCC 39006 and the plant pathogen Erwinia carotovora ssp. carotovora (Ecc), the biosynthes
27                          The enterobacterium Erwinia carotovora ssp. carotovora strain 71 (hereafter
28      The production of pectin lyase (Pnl) in Erwinia carotovora ssp. carotovora strain 71 is induced
29 re of the 40-kDa endo-polygalacturonase from Erwinia carotovora ssp. carotovora was solved by multipl
30 e include important plant pathogens, such as Erwinia carotovora subsp. atroseptica (Eca), the first p
31 (the elicitor of hypersensitive reaction) in Erwinia carotovora subsp. carotovora is regulated by Rsm
32                                              Erwinia carotovora subsp. carotovora produces an array o
33                                              Erwinia carotovora subsp. carotovora produces extracellu
34 , disease severity by the bacterial pathogen Erwinia carotovora subsp. carotovora was significantly r
35 ular protein production and pathogenicity in Erwinia carotovora subsp. carotovora.
36 uction and pathogenicity in soft rot-causing Erwinia carotovora subsp. carotovora.
37 nzymes, rsmB RNA, motility, and virulence of Erwinia carotovora subsp. carotovora.
38 virulence determinants in the phytopathogen, Erwinia carotovora subspecies carotovora.
39 acyl homoserine lactone (AHL) is required by Erwinia carotovora subspecies for the expression of vari
40                                           In Erwinia carotovora subspecies, N-acyl homoserine lactone

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