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首页> 外文期刊>Research journal of microbiology. >Identification of Potential Antifungal Metabolite Producing Pseudomonas tolaasii Strain GD76 Obtained from Contaminated Agar Plate
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Identification of Potential Antifungal Metabolite Producing Pseudomonas tolaasii Strain GD76 Obtained from Contaminated Agar Plate

机译:从污染的琼脂平板上获得潜在的抗真菌代谢物产生假单胞菌tolaasii菌株GD76的鉴定

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Background and Objective: Fungal pathogens develop resistance against antifungal agents available in market. Therefore, treatment of fungal infection is becoming problematic. On other hand, chemically synthesized antifungal agents are also causing adverse effect on human health. To overcome this issue, recently many drug industries are trying to isolate bioactive molecules from natural sources. The objective of the study was isolation and identification of bacterial isolate from contaminated agar plate with special reference to its antifungal property and explore bacterial contamination as new habitat for beneficial microbes. Materials and Methods: Antifungal metabolite producer Pseudomonas tolaasii ( P. tolaasii ) GD76 was isolated from contaminated yeast, peptone, dextrose (YPD) agar plate on to which it was streaked from casein agar plate. Morphological, biochemical and phylogenetic study was carried out for identification of the bacterial isolate by using 16S rRNA gene sequencing and evolutionary history was inferred using the maximum parsimony method. Results: Morphological and biochemical study of the bacterial isolate showed that the isolate was Gram negative, rod shape, capsule containing and ferment only glucose. On basis of position sequence of the isolate in phylogenetic tree, the isolate showed 99% similarity to Pseudomonas tolaasii , it is indicated that the isolate is the novel strain of P. tolaasii for which the name Pseudomonas tolaasii GD76 is affirm. Sequence of 16S rRNA gene was submitted to NCBI, Accession code; KU533778. Conclusion: On the basis of results obtained, present study indicates towards the potential of uncharacterized prokaryotic community associated with bacterial contamination.
机译:背景与目的:真菌病原体对市售的抗真菌剂产生抗药性。因此,真菌感染的治疗正成为问题。另一方面,化学合成的抗真菌剂也对人体健康造成不利影响。为了克服这个问题,最近许多制药行业都在尝试从自然资源中分离出生物活性分子。该研究的目的是从污染的琼脂板上分离和鉴定细菌分离物,并特别提及其抗真菌特性,并探索细菌污染作为有益微生物的新栖息地。材料和方法:抗真菌代谢物生产者Tolaasii(P. tolaasii)GD76从受污染的酵母,蛋白ept,右旋糖(YPD)琼脂平板上分离,并从酪蛋白琼脂平板上划线。进行了形态学,生化和系统发育研究,以通过16S rRNA基因测序鉴定细菌分离株,并使用最大简约方法推断了进化史。结果:该细菌分离物的形态和生化研究表明,该分离物为革兰氏阴性,棒状,仅含胶囊且仅发酵葡萄糖。根据分离株在系统树上的位置序列,该分离株与桃假单胞菌有99%的相似性,表明该分离株是新的桃假单胞菌菌株,其名称为假单胞菌GD76。 16S rRNA基因序列已提交NCBI,登录号; KU533778。结论:根据获得的结果,本研究表明了与细菌污染有关的原核生物群落的潜力。

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