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改进的生长培养基和培养技术,用于遗传分析和评估 Caldicellulosiruptor bescii 对生物质的利用。

Improved growth media and culture techniques for genetic analysis and assessment of biomass utilization by Caldicellulosiruptor bescii.

机构信息

Department of Genetics, University of Georgia, Athens, GA 30602, USA.

出版信息

J Ind Microbiol Biotechnol. 2013 Jan;40(1):41-9. doi: 10.1007/s10295-012-1202-1. Epub 2012 Nov 13.

Abstract

Methods for efficient growth and manipulation of relatively uncharacterized bacteria facilitate their study and are essential for genetic manipulation. We report new growth media and culture techniques for Caldicellulosiruptor bescii, the most thermophilic cellulolytic bacterium known. A low osmolarity defined growth medium (LOD) was developed that avoids problems associated with precipitates that form in previously reported media allowing the monitoring of culture density by optical density at 680 nm (OD(680)) and more efficient DNA transformation by electroporation. This is a defined minimal medium and does not support growth when a carbon source is omitted, making it suitable for selection of nutritional markers as well as the study of biomass utilization by C. bescii. A low osmolarity complex growth medium (LOC) was developed that dramatically improves growth and culture viability during storage, making it a better medium for routine growth and passaging of C. bescii. Both media contain significantly lower solute concentration than previously published media, allowing for flexibility in developing more specialized media types while avoiding the issues of growth inhibition and cell lysis due to osmotic stress. Plating on LOD medium solidified by agar results in ~1,000-fold greater plating efficiency than previously reported and allows the isolation of discrete colonies. These new media represent a significant advance for both genetic manipulation and the study of biomass utilization in C. bescii, and may be applied broadly across the Caldicellulosiruptor genus.

摘要

高效生长和操纵相对特征不明确的细菌的方法有助于它们的研究,并且对于遗传操作是必不可少的。我们报告了新的生长培养基和培养技术,用于最耐热的纤维素分解菌 Caldicellulosiruptor bescii。开发了一种低渗透压定义生长培养基(LOD),避免了以前报道的培养基中形成沉淀所带来的问题,允许通过 680nm 处的光密度(OD(680))监测培养密度,并通过电穿孔实现更有效的 DNA 转化。这是一种定义明确的最小培养基,如果省略碳源,则不支持生长,因此适合选择营养标记以及研究 C. bescii 对生物质的利用。开发了一种低渗透压复合生长培养基(LOC),可显著提高储存过程中的生长和培养活力,使其成为 C. bescii 常规生长和传代的更好培养基。这两种培养基的溶质浓度都明显低于以前发表的培养基,在开发更专门的培养基类型时具有更大的灵活性,同时避免了由于渗透压应激而导致的生长抑制和细胞裂解问题。在 LOD 培养基上凝固琼脂进行平板划线,比以前报道的方法提高了约 1000 倍的平板效率,并允许分离出离散的菌落。这些新的培养基代表了在 C. bescii 中的遗传操作和生物质利用研究方面的重大进展,并且可能广泛应用于 Caldicellulosiruptor 属。

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