Orro Alessandro, Cappelletti Martina, D'Ursi Pasqualina, Milanesi Luciano, Di Canito Alessandra, Zampolli Jessica, Collina Elena, Decorosi Francesca, Viti Carlo, Fedi Stefano, Presentato Alessandro, Zannoni Davide, Di Gennaro Patrizia
Institute of Biomedical Technology, CNR, Segrate, Milano, Italy.
Department of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.
PLoS One. 2015 Oct 1;10(10):e0139467. doi: 10.1371/journal.pone.0139467. eCollection 2015.
In this paper comparative genome and phenotype microarray analyses of Rhodococcus sp. BCP1 and Rhodococcus opacus R7 were performed. Rhodococcus sp. BCP1 was selected for its ability to grow on short-chain n-alkanes and R. opacus R7 was isolated for its ability to grow on naphthalene and on o-xylene. Results of genome comparison, including BCP1, R7, along with other Rhodococcus reference strains, showed that at least 30% of the genome of each strain presented unique sequences and only 50% of the predicted proteome was shared. To associate genomic features with metabolic capabilities of BCP1 and R7 strains, hundreds of different growth conditions were tested through Phenotype Microarray, by using Biolog plates and plates manually prepared with additional xenobiotic compounds. Around one-third of the surveyed carbon sources was utilized by both strains although R7 generally showed higher metabolic activity values compared to BCP1. Moreover, R7 showed broader range of nitrogen and sulphur sources. Phenotype Microarray data were combined with genomic analysis to genetically support the metabolic features of the two strains. The genome analysis allowed to identify some gene clusters involved in the metabolism of the main tested xenobiotic compounds. Results show that R7 contains multiple genes for the degradation of a large set of aromatic and PAHs compounds, while a lower variability in terms of genes predicted to be involved in aromatic degradation was found in BCP1. This genetic feature can be related to the strong genetic pressure exerted by the two different environment from which the two strains were isolated. According to this, in the BCP1 genome the smo gene cluster involved in the short-chain n-alkanes degradation, is included in one of the unique regions and it is not conserved in the Rhodococcus strains compared in this work. Data obtained underline the great potential of these two Rhodococcus spp. strains for biodegradation and environmental decontamination processes.
本文对红球菌属BCP1菌株和不透明红球菌R7进行了比较基因组和表型微阵列分析。选择红球菌属BCP1是因其能够在短链正构烷烃上生长,而不透明红球菌R7是因其能够在萘和邻二甲苯上生长而分离得到的。基因组比较结果,包括BCP1、R7以及其他红球菌参考菌株,表明每个菌株至少30%的基因组呈现独特序列,且只有50%的预测蛋白质组是共享的。为了将基因组特征与BCP1和R7菌株的代谢能力相关联,通过表型微阵列,使用Biolog平板以及手动制备的含有额外外源化合物的平板,测试了数百种不同的生长条件。尽管与BCP1相比,R7通常表现出更高的代谢活性值,但两种菌株利用了约三分之一的被调查碳源。此外,R7显示出更广泛的氮源和硫源范围。表型微阵列数据与基因组分析相结合,从遗传学角度支持了这两种菌株的代谢特征。基因组分析能够鉴定出一些参与主要测试外源化合物代谢的基因簇。结果表明,R7含有多个用于降解大量芳香族和多环芳烃化合物的基因,而在BCP1中,预测参与芳香族降解的基因变异性较低。这种遗传特征可能与分离这两种菌株的两种不同环境所施加的强大遗传压力有关。据此,在BCP1基因组中,参与短链正构烷烃降解的smo基因簇包含在一个独特区域中,并且在本研究中比较的红球菌菌株中不保守。所获得的数据强调了这两种红球菌属菌株在生物降解和环境净化过程中的巨大潜力。