BBSRC/EPSRC Synthetic Biology Research Centre, School of Life Sciences, University of Nottingham, Nottingham, NG7 2RD, UK.
University of New-South Wales (UNSW) Sydney, Kensington, Australia.
Appl Microbiol Biotechnol. 2019 Jun;103(11):4633-4648. doi: 10.1007/s00253-019-09763-6. Epub 2019 Apr 10.
Clostridium autoethanogenum and Clostridium ljungdahlii are physiologically and genetically very similar strict anaerobic acetogens capable of growth on carbon monoxide as sole carbon source. While exact nutritional requirements have not been reported, we observed that for growth, the addition of vitamins to media already containing yeast extract was required, an indication that these are fastidious microorganisms. Elimination of complex components and individual vitamins from the medium revealed that the only organic compounds required for growth were pantothenate, biotin and thiamine. Analysis of the genome sequences revealed that three genes were missing from pantothenate and thiamine biosynthetic pathways, and five genes were absent from the pathway for biotin biosynthesis. Prototrophy in C. autoethanogenum and C. ljungdahlii for pantothenate was obtained by the introduction of plasmids carrying the heterologous gene clusters panBCD from Clostridium acetobutylicum, and for thiamine by the introduction of the thiC-purF operon from Clostridium ragsdalei. Integration of panBCD into the chromosome through allele-coupled exchange also conveyed prototrophy. C. autoethanogenum was converted to biotin prototrophy with gene sets bioBDF and bioHCA from Desulfotomaculum nigrificans strain CO-1-SRB, on plasmid and integrated in the chromosome. The genes could be used as auxotrophic selection markers in recombinant DNA technology. Additionally, transformation with a subset of the genes for pantothenate biosynthesis extended selection options with the pantothenate precursors pantolactone and/or beta-alanine. Similarly, growth was obtained with the biotin precursor pimelate combined with genes bioYDA from C. acetobutylicum. The work raises questions whether alternative steps exist in biotin and thiamine biosynthesis pathways in these acetogens.
产酸克雷伯氏菌和热自养梭菌在生理学和遗传学上非常相似,都是严格的厌氧产乙酸菌,能够以一氧化碳作为唯一的碳源进行生长。虽然确切的营养需求尚未报道,但我们观察到,为了生长,需要在已经含有酵母提取物的培养基中添加维生素,这表明这些是苛刻的微生物。从培养基中去除复杂成分和个别维生素表明,生长所需的唯一有机化合物是泛酸、生物素和硫胺素。基因组序列分析表明,泛酸和硫胺素生物合成途径中有 3 个基因缺失,生物素生物合成途径中有 5 个基因缺失。通过引入携带来自丙酮丁醇梭菌的异源基因簇 panBCD 的质粒,产酸克雷伯氏菌和热自养梭菌获得了泛酸的原养型,通过引入来自拉氏梭菌的 thiC-purF 操纵子,获得了硫胺素的原养型。通过等位基因偶联交换将 panBCD 整合到染色体中也赋予了原养型。通过从脱硫脱硫弧菌 CO-1-SRB 菌株的 bioBDF 和 bioHCA 基因集,将产酸克雷伯氏菌转化为生物素原养型,该基因集在质粒上并整合到染色体中。这些基因可用作重组 DNA 技术中的营养缺陷型选择标记。此外,通过部分泛酸生物合成基因的转化,增加了泛酸前体泛酸内酯和/或β-丙氨酸的选择选项。同样,与丙酮丁醇梭菌的 bioYDA 基因结合,也可以用生物素前体 pimelate 获得生长。这项工作提出了这样一个问题,即在这些产乙酸菌的生物素和硫胺素生物合成途径中是否存在替代步骤。