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首页> 外文期刊>Journal of Drug Delivery and Therapeutics >IDENTIFICATION OF ACTINOMYCETYES IN THE BIODEGRADED WALL MATERIAL BY PCR AMPLIFIED GENE FRAGMENT CODING FOR 16S rRNA
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IDENTIFICATION OF ACTINOMYCETYES IN THE BIODEGRADED WALL MATERIAL BY PCR AMPLIFIED GENE FRAGMENT CODING FOR 16S rRNA

机译:PCR扩增的16S rRNA基因片段编码鉴定生物降解墙材料中的放线菌

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摘要

Generally, old buildings and monuments are often affected by biodecay. An inventory of the existing microbial consortia which associated with the damage part of the buildings wall is not yet integral part of the restoration process. This stems from the lack of effective means for such stocktaking. Although, Actinomycetes, fungi and bacteria cause severe damage through mechanical process from the growth into wall and its grounding and through their metabolism. Physiological and molecular approach based techniques were used in the detection and identification of DNA sequences encoding rRNA to actinomycetes present on building wall. DNA from isolate was extracted and 194 basepair fragments of the 16S rDNA were amplified with cultured primers. The 16S rDNA fragments of uniform length obtained from the different species were separated according to their sequences difference by PCR. By the sequencing excised and reamplified individual DNA bands, characterized the phylogenetic tree of corresponding actinomycetes. Using this approach, we identified members of the genera of Streptomyces , Nocardia and Micromonospora .
机译:通常,旧建筑物和古迹经常受到生物衰变的影响。与建筑物墙壁的损坏部分相关的现有微生物联合体的清单还不是恢复过程的组成部分。这是由于缺乏有效的盘点方法。尽管放线菌,真菌和细菌通过从生长到壁和其根部的机械过程以及通过它们的新陈代谢而引起严重破坏。基于生理和分子方法的技术被用于检测和鉴定编码存在于建筑物墙壁上的放线菌的rRNA的DNA序列。提取分离物的DNA,并用培养的引物扩增194个16S rDNA碱基对片段。从不同物种获得的等长的16S rDNA片段根据其序列差异通过PCR进行分离。通过测序切除并扩增单个DNA条带,表征了相应放线菌的系统树。使用这种方法,我们确定了链霉菌,诺卡氏菌和微单孢菌属的成员。

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