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Characterization of the rrnB Operon of the Plant Pathogen Rhodococcus fascians and Targeted Integrations of Exogenous Genes at rrn Loci

机译:植物病原菌红球菌的rrnB操纵子的表征和rrn基因座上的外源基因的靶向整合。

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摘要

A 6.0-kb SalI DNA fragment containing an entire rRNA operon (rrnB) was cloned from a cosmid gene bank of the phytopathogenic strain Rhodococcus fascians D188. The nucleotide sequence of the 6-kb fragment was determined and had the organization 16S rRNA-spacer-23S rRNA-spacer-5S rRNA without tRNA-encoding genes in the spacer regions. The 5′ and 3′ ends of the mature 16S, 23S, and 5S rRNAs were determined by alignment with the rrn operons of Bacillus subtilis and other gram-positive bacteria. Four copies of the rrn operons were identified by hybridization with an rrnB probe in R. fascians type strain ATCC 12974 and in the virulent strain R. fascians D188. However, another isolate, CECT 3001 (= NRRL ), also classified as R. fascians, produced five rrn-hybridizing bands. An integrative vector containing a 2.5-kb DNA fragment internal to rrnB was constructed for targeted integration of exogenous genes at the rrn loci. Transformants carrying the exogenous chloramphenicol resistance gene (cmr) integrated in different rrn operons were obtained. These transformants had normal growth rates in complex medium and minimal medium and were fully stable for the integrated marker.
机译:从植物致病菌株法氏红球菌D188的粘粒基因库中克隆了一个包含整个rRNA操纵子(rrnB)的6.0-kb SalI DNA片段。确定了6kb片段的核苷酸序列,并具有在间隔区中没有tRNA编码基因的组织16S rRNA-间隔子-23S rRNA-间隔子-5S rRNA。成熟的16S,23S和5S rRNA的5'和3'末端通过与枯草芽孢杆菌和其他革兰氏阳性细菌的rrn操纵子对齐来确定。通过在r。fascians型菌株ATCC 12974和强力R. fascians D188菌株中与rrnB探针杂交鉴定出四个拷贝的rrn操纵子。但是,另一种分离株CECT 3001(= NRRL)也被分类为法西斯菌(R. fascians),产生了五个rrn杂交带。构建了包含rrnB内部的2.5-kb DNA片段的整合载体,用于在rrn基因座上靶向整合外源基因。获得了带有整合在不同rrn操纵子中的外源氯霉素抗性基因(cmr)的转化体。这些转化子在复杂培养基和基本培养基中均具有正常的生长速率,并且对于整合标记物而言是完全稳定的。

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