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Flocculation-Related Gene Identification by Whole-Genome Sequencing of Thauera aminoaromatica MZ1T Floc-Defective Mutants

机译:拟南芥MZ1T絮凝缺陷突变体全基因组测序的絮凝相关基因鉴定

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摘要

Thauera aminoaromatica MZ1T, a floc-forming bacterium isolated from an industrial activated-sludge wastewater treatment plant, overproduces exopolysaccharide (EPS), leading to viscous bulking. This phenomenon results in poor sludge settling and dewatering during the clarification process. To identify genes responsible for bacterial flocculation, a whole-genome phenotypic-sequencing technique was applied. Genomic DNA of MZ1T flocculation-deficient mutants was subjected to massively parallel sequencing. The resultant high-quality reads were assembled and compared to the reference genome of the wild type (WT). We identified nine nonsynonymous mutations and one nonsense mutation putatively involved in EPS biosynthesis. Complementation of the nonsense mutation located in an EPS deacetylase gene restored the flocculating phenotype. The Fourier transform infrared (FTIR) spectra of EPS isolated from the wild type showed a reduced C=O peak of the N-acetyl group at 1,665 cm−1 compared to the spectra of MZ1T floc-deficient mutant EPS, suggesting that the WT EPS was partially deacetylated. Gene expression analysis also demonstrated that the putative deacetylase gene transcript increased before flocculation occurred. These data suggest that targeting deacetylation processes via direct chemical modification of EPS or enzyme inhibition may prove useful in combating viscous bulking in this and related bacteria.
机译:从工业活性污泥废水处理厂分离出的絮状细菌Thauera aminoaromatica MZ1T过量生产胞外多糖(EPS),导致粘性膨胀。这种现象导致澄清过程中的污泥沉淀和脱水不良。为了鉴定负责细菌絮凝的基因,应用了全基因组表型测序技术。对MZ1T絮凝缺陷型突变体的基因组DNA进行大规模平行测序。组装得到的高质量读段,并与野生型(WT)的参考基因组进行比较。我们确定了9个非同义突变和1个无意义的突变,它们可能参与了EPS生物合成。位于EPS脱乙酰基酶基因中的无意义突变的补充恢复了絮凝表型。与MZ1T絮凝缺陷型突变体的光谱相比,从野生型中分离得到的EPS的傅立叶变换红外光谱显示N-乙酰基的C = O峰在1,665 cm -1 处降低。 EPS,表明WT EPS已部分脱乙酰。基因表达分析还表明,在絮凝发生之前,假定的脱乙酰基酶基因转录本增加了。这些数据表明,通过EPS的直接化学修饰或酶抑制作用靶向脱乙酰基过程可证明可用于对抗这种细菌和相关细菌中的粘性膨胀。

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