• Journal of the Korean Society of Tobacco Science
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• v.18 no.1
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• pp.60-65
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• 1996

Chemicals including antibiotics and bactericides were screened for suppression of streptomycin-resistant Erwinia cmutouom subsp. cmutovom (Ecc) strains in laboratory and field conditions. Oxytetracycline, ethoquinolac and dichlorophen suppressed the growth of streptomycin-resistant Ecc strains in vitro. Fractional inhibitory concentration (FIC) indices of oxytetracycline and ethoquinolac mixed with streptomycin against the Ecc strains were equal to and less than one, respectively. Consequently the efficacy of those chemicals in mixture with sorptomycin were non-antagonistic But that of dichlorophen mixed with streptomycin was more than one, therefore the efficacy of the mixture was antagonistic. Spray of oxyteoucycline, ethoquinolac and agrimycin-100 on the topped burley tobacco plants was efficacious in reducing tobacco hollow stalk at the same level of sorptomycin treatment in three-year field trials, which suggests that those are promising chemicals to be alternative to streptomycin for control of tobacco hollow stalk.

• Journal of the Korean Society of Tobacco Science
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• v.11 no.1
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• pp.41-48
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• 1989

The significance of soil and/or rhisosphere populations of Erwinia carotovora sobsp. carotovora (Ecc) as a source of primary inoculum for tobacco hollow stalk disease has been demonstrated conclusively. The survival of Ecc in field soils fter overwintering was estimated by using the enrichment technique. The population number of pectolytic erwinia (PE) in field soils relatively decreased at the rate of 102-104 colony forming unit(CFU) per g of soil after overwintering. Higher level of PE population overwintered in the rhlzosphere foils of tobacco stubbles and detected more frequently in rhizosphere soils of weed plants than in those of bare fields. All of the tobacco stubbles collected from fields where tobacco had been grown the previous year contained Ecc. The more survived population number of PE at the 30cm depth of artifitiany infested soils than at the upper of those by introducing with diseased tobacco plant tissue after overwintering. Ecc overwintered effectively in rhizosphere soils of tobacco stubbles, overwintered weeds and tobacco debris in field soils.

• Applied Biological Chemistry
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• v.40 no.5
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• pp.380-387
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• 1997

Phytopathogenic Erwinia carotovora subsp. carotovora (Ecc) LY34 causes plant tissue maceration by secretion of pectinolytic enzymes such as pectate Iyase (PL) existed as multiple isoenzyme form. Genomic DNA from Ecc LY34 was digested with Sau3Al and ligated into the BamHI site of pBluescript ll $SK^+$. Among them, a clone hydrolyzing polypectate was selected and its DNA was digested with BamHI. Through the subsequent subcloning the resulting 3.1 kb fragment, corresponding to a peICI, was subcloned into pLYPA 100. The structural organization of a peICI gene encoding a 374 amino acid residues consists of an open reading frame (ORF) of 1,122 bp commencing with a ATG start codon and followed by a TAA stop codon. PeICI contained a typical prokaryotic signal peptide of 22-amino acid. Since the deduced amino acid sequences of PeICl protein was very similar to those of PelIII of Erwinia carotovora subsp. carotovora, and to those of Pel3 of Erwinia carotovora subsp. atroseptica, and to those of PeIC of Erwinia carotovora subsp. carotovora, it belong to the same family PLbc group. The 374-amino acld PeICI had a calculated Mr of 40,507 and pI of 7.60.