首页> 外文OA文献 >Identification and nucleotide sequence of Rhizobium meliloti insertion sequence ISRm3: similarity between the putative transposase encoded by ISRm3 and those encoded by Staphylococcus aureus IS256 and Thiobacillus ferrooxidans IST2.
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Identification and nucleotide sequence of Rhizobium meliloti insertion sequence ISRm3: similarity between the putative transposase encoded by ISRm3 and those encoded by Staphylococcus aureus IS256 and Thiobacillus ferrooxidans IST2.

机译:苜蓿根瘤菌插入序列ISRm3的鉴定和核苷酸序列:由ISRm3编码的推定转座酶与由金黄色葡萄球菌IS256和氧化亚铁硫杆菌IST2编码的推定转座酶之间的相似性。

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摘要

The insertion sequence ISRm3 was discovered simultaneously in different Rhizobium meliloti strains by probing Southern blots of total cellular DNA with 32P-labeled pTA2. This plasmid is indigenous to strain IZ450 and fortuitously contained four copies of ISRm3. By using an internal EcoRI fragment as a specific probe (pRWRm31), homology to ISRm3 was subsequently detected in over 90% of R. meliloti strains tested from different geographical locations around the world. The frequency of stable nonlethal ISRm3 transpositions was estimated to be 4 x 10(-5) per generation per cell in strain SU47 when grown in liquid culture. The entire nucleotide sequence of ISRm3 in R. meliloti 102F70 is 1,298 bp and has 30-bp terminal inverted repeats which are perfectly matched. Analysis of six copies of ISRm3 in two strains showed that a variable number of base pairs (usually eight or nine) were duplicated and formed direct repeats adjacent to the site of insertion. On one DNA strand, ISRm3 contains an open reading frame spanning 93% of its length. Comparison of the putative protein encoded with sequences derived from the EMBL and GenBank databases showed significant similarity between the putative transposases of ISRm3 from R. meliloti, IS256 from Staphylococcus aureus, and IST2 from Thiobacillus ferroxidans. These insertion sequences appear to be distantly related members of a distinct class.
机译:通过用32P标记的pTA2探测总细胞DNA的Southern印迹,在不同的苜蓿根瘤菌菌株中同时发现了插入序列ISRm3。该质粒是菌株IZ450固有的,偶然地含有4个ISRm3拷贝。通过使用内部EcoRI片段作为特异性探针(pRWRm31),随后在来自全球不同地理位置的90%的苜蓿根瘤菌中检测到与ISRm3的同源性。当在液体培养物中生长时,菌株SU47中稳定的非致死ISRm3转座的频率估计为每细胞每代4×10(-5)。 R. meliloti 102F70中ISRm3的整个核苷酸序列为1,298 bp,具有30 bp的末端反向重复序列,这些序列完全匹配。对两个菌株中6个ISRm3拷贝的分析表明,重复了可变数目的碱基对(通常为8个或9个),并在插入位点附近形成了直接重复序列。在一条DNA链上,ISRm3包含一个开放阅读框,跨越其长度的93%。用来自EMBL和GenBank数据库的序列编码的推定蛋白质进行比较,结果表明,R。meliloti的ISRm3转座酶,金黄色葡萄球菌的IS256和铁氧化硫杆菌的IST2推定的转座酶之间存在显着相似性。这些插入序列似乎是不同类别的远距离相关成员。

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    Wheatcroft, R; Laberge, S;

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  • 年度 1991
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  • 原文格式 PDF
  • 正文语种 en
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