Klieve Athol V, Yokoyama Melvin T, Forster Robert J, Ouwerkerk Diane, Bain Peter A, Mawhinney Erin L
Department of Primary Industries and Fisheries, Animal Science, Yeerongpilly, Queensland 4105, Australia.
Appl Environ Microbiol. 2005 Aug;71(8):4248-53. doi: 10.1128/AEM.71.8.4248-4253.2005.
A genetic transformation system with similarities to those reported for gram-negative bacteria was found to be associated with membrane vesicles of the ruminal cellulolytic genus Ruminococcus. Double-stranded DNA was recovered from the subcellular particulate fraction of all the cellulolytic ruminococci examined. Electron microscopy revealed that the only particles present resembled membrane vesicles. The likelihood that the DNA was associated with membrane vesicles (also known to contain cellulosomes) was further supported by the adherence of the particles associated with the subcellular DNA to cellulose powder added to culture filtrates. The particle-associated DNA comprised a population of linear molecules ranging in size from <20 kb to 49 kb (Ruminococcus sp. strain YE73) and from 23 kb to 90 kb (Ruminococcus albus AR67). Particle-associated DNA from R. albus AR67 represented DNA derived from genomic DNA of the host bacterium having an almost identical HindIII digestion pattern and an identical 16S rRNA gene. Paradoxically, particle-associated DNA was refractory to digestion with EcoRI, while the genomic DNA was susceptible to extensive digestion, suggesting that there is differential restriction modification of genomic DNA and DNA exported from the cell. Transformation using the vesicle-containing fraction of culture supernatant of Ruminococcus sp. strain YE71 was able to restore the ability to degrade crystalline cellulose to two mutants that were otherwise unable to do so. The ability was heritable and transferred to subsequent generations. It appears that membrane-associated transformation plays a role in lateral gene transfer in complex microbial ecosystems, such as the rumen.
发现一种与革兰氏阴性菌中报道的系统相似的遗传转化系统与瘤胃纤维素分解菌属瘤胃球菌的膜泡有关。从所有检测的纤维素分解瘤胃球菌的亚细胞颗粒部分中回收了双链DNA。电子显微镜显示,存在的唯一颗粒类似于膜泡。与亚细胞DNA相关的颗粒与添加到培养滤液中的纤维素粉末的粘附进一步支持了DNA与膜泡(也已知含有纤维小体)相关的可能性。与颗粒相关的DNA由一群线性分子组成,其大小范围为<20 kb至49 kb(瘤胃球菌属菌株YE73)和23 kb至90 kb(白色瘤胃球菌AR67)。来自白色瘤胃球菌AR67的与颗粒相关的DNA代表来自宿主细菌基因组DNA的DNA,其具有几乎相同的HindIII消化模式和相同的16S rRNA基因。矛盾的是,与颗粒相关的DNA对EcoRI消化具有抗性,而基因组DNA则易于广泛消化,这表明基因组DNA和从细胞输出的DNA存在差异限制修饰。使用瘤胃球菌属菌株YE71培养上清液中含囊泡部分进行转化能够恢复两种原本无法降解结晶纤维素的突变体降解结晶纤维素的能力。这种能力是可遗传的,并能传递给后代。看来与膜相关的转化在复杂的微生物生态系统(如瘤胃)的横向基因转移中起作用。