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作 者:杨勇[1] 钟莉[1] 田新莉[1] 成秋香[1] 陈振华[1] 覃重军[1]
机构地区:[1]中国科学院上海生命科学研究院,植物生理生态研究所合成生物学重点实验室,上海200032
出 处:《微生物学报》2010年第4期452-458,共7页Acta Microbiologica Sinica
基 金:国家自然科学基金(30870067;30770045;30325003);国家"863计划"(2007AA021503);中国科学院知识创新工程项目(KSCX2-YW-G-014)~~
摘 要:从小葱植物中分离到一株编号为36R-2-1B的链霉菌菌株,该菌株含有一个约为280kb的线型质粒pYY8L。【目的】克隆、测序和分析pYY8L新的端粒和复制区。【方法】采用改良的"在凝胶中进行DNA碱处理与酶切"的方法来克隆大的线型质粒pYY8L的端粒,通过构建基因组柯斯文库和次级克隆的方法来缩小和鉴定pYY8L的复制区。【结果】在小葱植物内生链霉菌36R-2-1B中检测到约为280kb的线型质粒pYY8L,克隆了pYY8L的端粒。其末端的152bp包含6个小的回文序列,可以形成复杂的二级结构。利用柯斯文库构建、次级克隆和测序获得了4891bp的pYY8L的复制区。该复制区含有6个基因,其中2个与天蓝色链霉菌线型质粒SCP1的复制基因非常相似,但是邻近的重复序列不同。【结论】采用新的改良的方法克隆和鉴定了pYY8L新的端粒和复制区。本文首次报道了植物内生链霉菌线型质粒的端粒和复制基因。Strain 36R-2-1B was isolated from Allium fistulosum and identified as Streptomyces spp.,harboring a ~ 280 kb linear plasmid designated pYY8L.ObjectiveCloning,sequencing and analysis of telomere and internal replication origin of pYY8L.MethodspYY8L telomere was cloned by a modified procedure ─"alkaline treatment and enzyme digestion in gel".The internal replication origin of pYY8L was cloned by construction of a cosmid library and then sub-cloning.ResultsA ~ 280 kb DNA band(pYY8L) of strain 36R-2-1B was detected by pulsed-field gel electrophoresis.The 152-bp telomere,containing six small palindromes and potentially forming complicated secondary structure,was cloned and sequenced.The replication origin of pYY8L was initially cloned on a cosmid and then sub-cloned as a 4891-bp autonomous replication sequence.This sequence was predicted to contain six genes,two of them resembling replication genes of Streptomyces linear plasmid SCP1,but their adjacent iterons were different.ConclusionNew telomere and internal replication origin of Streptomyces linear plasmid pYY8L were cloned and identified.This is the first example of report on telomere and replication genes of linear plasmid from endophytic Streptomyces.
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