HOMOLOGOUS STREPTOMYCIN RESISTANCE GENE PRESENT AMONG DIVERSE GRAM-NEGATIVE BACTERIA IN NEW-YORK-STATE APPLE ORCHARDS

被引:38
作者
NORELLI, JL
BURR, TJ
LOCICERO, AM
GILBERT, MT
KATZ, BH
机构
关键词
D O I
10.1128/AEM.57.2.486-491.1991
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The streptomycin resistance gene of Pseudomonas syringae pv. papulans Psp36 was cloned into Escherichia coli and used to develop a 500-bp DNA probe that is specific for streptomycin resistance in P. syringae pv. papulans. The probe is a portion of a 1-kb region shared by three different DNA clones of the resistance gene. In Southern hybridizations, the probe hybridized only with DNA isolated from streptomycin-resistant strains of P. syringae pv. papulans and not with the DNA of streptomycin-sensitive strains. Transposon insertions within the region of DNA shared by the three clones resulted in loss of resistance to streptomycin. Colony hybridization of bacteria isolated from apple leaves and orchard soil indicated that 39% of 398 streptomycin-resistant bacteria contained DNA that hybridized to the probe. These included all strains of P. syringae pv. papulans and some other fluorescent pseudomonads and nonfluorescent gram-negative bacteria, but none of the gram-positive bacteria. The same-size restriction fragments hybridized to the probe in P. syringae pv. papulans. Restriction fragment length polymorphism of this region was occasionally observed in strains of other taxonomic groups of bacteria. In bacteria other than P. syringae pv. papulans, the streptomycin resistance probe hybridized to different-sized plasmids and no relationship between plasmid size and taxonomic group or between plasmid size and orchard type, soil association, or leaf association could be detected.
引用
收藏
页码:486 / 491
页数:6
相关论文
共 31 条
[1]  
BIRNBOIM HC, 1983, METHOD ENZYMOL, V100, P243
[2]   STREPTOMYCIN RESISTANCE OF PSEUDOMONAS-SYRINGAE PV PAPULANS IN APPLE ORCHARDS AND ITS ASSOCIATION WITH A CONJUGATIVE PLASMID [J].
BURR, TJ ;
NORELLI, JL ;
KATZ, B ;
WILCOX, WF ;
HOYING, SA .
PHYTOPATHOLOGY, 1988, 78 (04) :410-413
[3]  
BURR TJ, 1979, PLANT DIS REP, V63, P157
[4]  
BURR TJ, 1981, PLANT DIS, V65, P334, DOI 10.1094/PD-65-334
[5]  
CHATTERJEE AK, 1973, J BACTERIOL, V112, P567
[6]  
Davies JE., 1986, ANTIBIOTICS LABORATO, P790
[7]  
DHANVANTARI BN, 1977, NEW ZEAL J AGR RES, V20, P557
[8]  
ELLIS MA, COMMUNICATION
[9]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[10]   STUDIES ON TRANSFORMATION OF ESCHERICHIA-COLI WITH PLASMIDS [J].
HANAHAN, D .
JOURNAL OF MOLECULAR BIOLOGY, 1983, 166 (04) :557-580