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一种分离产铁载体放线菌的新方法。

A new approach to isolating siderophore-producing actinobacteria.

机构信息

School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool, UK.

出版信息

Lett Appl Microbiol. 2012 Jul;55(1):68-72. doi: 10.1111/j.1472-765X.2012.03259.x. Epub 2012 May 17.

Abstract

AIMS

This study was conducted to investigate the application of 2,2'-dipyridyl as a new approach to isolating siderophore-producing actinobacteria.

METHODS AND RESULTS

Isolation of actinobacteria from soil was conducted by a soil dilution plate technique using starch-casein agar. Iron starvation was fostered by the incorporation of the iron chelator 2,2'-dipyridyl in the isolation medium. Pretreatment of the samples at an elevated temperature (40°C) ensured that the majority of nonsporulating bacteria were excluded. The survivors of this treatment were largely actinobacteria. Of the viable cultures grown in the presence of 2,2'-dipyridyl, more than 78-88% (average of three separate studies) were reported to produce siderophore-like compounds compared to 13-18% (average of three separate studies) when grown on the basic media in the absence of the chelating agent. The most prolific producers as assessed by the chrome azurol sulphate (CAS) assay were further characterized and found to belong to the genus Streptomyces.

CONCLUSIONS

Selective pressure using 2,2'-dipyridyl as an iron-chelating agent in starch-casein media increased the isolation of siderophore-producing actinobacteria compared to the unamended medium.

SIGNIFICANCE AND IMPACT OF THE STUDY

The study described represents a new approach to the isolation of siderophore-producing actinobacteria using a novel procedure that places a selection on cell population based upon the incorporation of a chelating agent in the medium.

摘要

目的

本研究旨在探索 2,2'-联吡啶作为一种分离产铁载体放线菌的新方法的应用。

方法和结果

采用淀粉-酪蛋白琼脂进行土壤稀释平板技术从土壤中分离放线菌。通过在分离培养基中加入铁螯合剂 2,2'-联吡啶来促进铁饥饿。在高温(40°C)下对样品进行预处理,以确保大多数非孢子形成细菌被排除。经过这种处理的幸存者主要是放线菌。在 2,2'-联吡啶存在的情况下生长的可培养培养物中,据报道,超过 78-88%(三个独立研究的平均值)产生了类似于铁载体的化合物,而在没有螯合剂的基础培养基上生长时,这一比例为 13-18%(三个独立研究的平均值)。通过铬天青 S(CAS)测定评估,最具生产力的生产者进一步被表征,并发现它们属于链霉菌属。

结论

在淀粉-酪蛋白培养基中使用 2,2'-联吡啶作为铁螯合剂进行选择性压力,与未改良的培养基相比,增加了产铁载体放线菌的分离。

研究的意义和影响

本研究描述了一种使用新型程序分离产铁载体放线菌的新方法,该程序通过在培养基中加入螯合剂对细胞群体进行选择。

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