Reeves Andrew R, Post David A, Vanden Boom Thomas J
Abbott Laboratories, Fermentation Microbiology Research and Development1401 Sheridan Road, North Chicago, IL 60064-4000USA.
Microbiology (Reading). 1998 Aug;144 ( Pt 8):2151-2159. doi: 10.1099/00221287-144-8-2151.
A physical map of the chromosome of the erythromycin-producing actinomycete Saccharopolyspora erythraea NRRL 2338 has been constructed using the restriction enzymes AseI and DraI. The map was constructed by a variety of methods including linking clone analysis, cross-hybridizations using labelled macrorestriction fragments, gene probing, two-dimensional PFGE and restriction enzyme site generation. Analysis of the individual macrorestriction patterns of the 17 AseI-, 6 DraI- and 22 AseI/DraI-digested fragments indicated a chromosome size of about 8 Mb. Linking clones for five contiguous AseI fragments were obtained, covering 32% of the chromosome. The linkage of an additional eight AseI fragments was aided by the finding that the rRNA operons of S. erythraea contain an AseI site within the 16S (rrs) gene. Generation of S. erythraea strains that contain additional DraI sites within selected AseI fragments, followed by PFGE analysis and Southern hybridization to determine specific linkages, facilitated the completion of the AseI map. The entire DraI map was constructed by gene probing and cross-hybridizations. PFGE analysis of agarose-embedded DNA prepared in either the presence or absence of proteinase K suggested that the S. erythraea NRRL 2338 chromosome is linear. A total of 15 genes or gene clusters were mapped to specific AseI and DraI fragments, including the erythromycin-biosynthetic gene cluster and the rRNA operons.
利用限制性内切酶AseI和DraI构建了产红霉素放线菌糖多孢红霉菌NRRL 2338的染色体物理图谱。该图谱通过多种方法构建,包括连锁克隆分析、使用标记的大限制性片段进行交叉杂交、基因探测、二维脉冲场凝胶电泳(PFGE)以及限制性酶切位点生成。对17个AseI酶切片段、6个DraI酶切片段和22个AseI/DraI双酶切片段的单个大限制性图谱分析表明,染色体大小约为8 Mb。获得了五个连续AseI片段的连锁克隆,覆盖了染色体的32%。红霉菌的rRNA操纵子在16S(rrs)基因内含有一个AseI位点,这有助于另外八个AseI片段的连锁分析。通过在选定的AseI片段中产生含有额外DraI位点的红霉菌菌株,随后进行PFGE分析和Southern杂交以确定特定的连锁关系,促进了AseI图谱的完成。整个DraI图谱通过基因探测和交叉杂交构建。对在有或无蛋白酶K的情况下制备的琼脂糖包埋DNA进行PFGE分析表明,糖多孢红霉菌NRRL 2338的染色体是线性的。总共15个基因或基因簇被定位到特定的AseI和DraI片段上,包括红霉素生物合成基因簇和rRNA操纵子。