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克服限制作为 Caldicellulosiruptor 物种中 DNA 转化的障碍可导致高效的标记替换。

Overcoming restriction as a barrier to DNA transformation in Caldicellulosiruptor species results in efficient marker replacement.

机构信息

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

出版信息

Biotechnol Biofuels. 2013 May 29;6(1):82. doi: 10.1186/1754-6834-6-82.

Abstract

BACKGROUND

Thermophilic microorganisms have special advantages for the conversion of plant biomass to fuels and chemicals. Members of the genus Caldicellulosiruptor are the most thermophilic cellulolytic bacteria known. They have the ability to grow on a variety of non-pretreated biomass substrates at or near ~80°C and hold promise for converting biomass to bioproducts in a single step. As for all such relatively uncharacterized organisms with desirable traits, the ability to genetically manipulate them is a prerequisite for making them useful. Metabolic engineering of pathways for product synthesis is relatively simple compared to engineering the ability to utilize non-pretreated biomass.

RESULTS

Here we report the construction of a deletion of cbeI (Cbes2438), which encodes a restriction endonuclease that is as a major barrier to DNA transformation of C. bescii. This is the first example of a targeted chromosomal deletion generated by homologous recombination in this genus and the resulting mutant, JWCB018 (ΔpyrFA ΔcbeI), is readily transformed by DNA isolated from E. coli without in vitro methylation. PCR amplification and sequencing suggested that this deletion left the adjacent methyltransferase (Cbes2437) intact. This was confirmed by the fact that DNA isolated from JWCB018 was protected from digestion by CbeI and HaeIII. Plasmid DNA isolated from C. hydrothermalis transformants were readily transformed into C. bescii. Digestion analysis of chromosomal DNA isolated from seven Caldicellulosiruptor species by using nine different restriction endonucleases was also performed to identify the functional restriction-modification activities in this genus.

CONCLUSION

Deletion of the cbeI gene removes a substantial barrier to routine DNA transformation and chromosomal modification of C. bescii. This will facilitate the functional analyses of genes as well as metabolic engineering for the production of biofuels and bioproducts from biomass. An analysis of restriction-modification activities in members of this genus suggests a way forward to eliminating restriction as a barrier to DNA transformation and efficient genetic manipulation of this important group of hyperthermophiles.

摘要

背景

嗜热微生物在将植物生物质转化为燃料和化学品方面具有特殊优势。已知的最耐热纤维素分解菌属是 Caldicellulosiruptor 属的成员。它们能够在 80°C 左右或接近 80°C 的各种未经预处理的生物质基质上生长,并有望在一步中将生物质转化为生物制品。对于所有具有理想特性的此类相对特征不明显的生物体,能够对其进行遗传操作是使其有用的前提条件。与工程化利用未经预处理的生物质的能力相比,产物合成途径的代谢工程相对简单。

结果

本文报道了 cbeI(Cbes2438)基因缺失的构建,该基因编码一种限制内切酶,是 C. bescii 进行 DNA 转化的主要障碍。这是该属中通过同源重组产生的第一个靶向染色体缺失的例子,所得突变体 JWCB018(ΔpyrFAΔcbeI)很容易被从大肠杆菌中分离出的 DNA 转化,而无需体外甲基化。PCR 扩增和测序表明,该缺失使相邻的甲基转移酶(Cbes2437)保持完整。从 JWCB018 中分离出的 DNA 不受 CbeI 和 HaeIII 消化的事实证实了这一点。从 C. hydrothermalis 转化子中分离出的质粒 DNA 很容易转化为 C. bescii。还使用九种不同的限制内切酶对来自七种 Caldicellulosiruptor 物种的染色体 DNA 进行了消化分析,以鉴定该属中的功能限制修饰活性。

结论

cbeI 基因的缺失消除了 C. bescii 常规 DNA 转化和染色体修饰的主要障碍。这将促进基因的功能分析以及从生物质生产生物燃料和生物制品的代谢工程。对该属成员中限制修饰活性的分析为消除限制作为 DNA 转化的障碍和对这群重要的高温嗜热菌进行高效遗传操作提供了一种方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bbe/3679861/1c83098061f5/1754-6834-6-82-1.jpg

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