[Mechanism of Action of Activated Sludge Properties in Nitrogen Removal by Endogenous Denitrification Through an Intelligent Aeration-controlled A/O Process].

In order to evaluate the mechanism of action of activated sludge properties in nitrogen removal by endogenous denitrification (henceforth EDNR), a new kind of automatic oxygen supply device(AOSD), was applied to the A/O process. The domestication effect of the aeration mode on the activated sludge properties and microbial communities was investigated under the intelligent aeration-controlled A/O process (I-A/O)and the continuous aeration A/O process (C-A/O). The results demonstrated that the effluent NH4+-N and NO2--N components showed obvious accumulation efficiencies and activated sludge generated conspicuous limited bulking in the I-A/O process. Domesticated sludge in the I-A/O process was able to enrich more SCOD to transfer into the polymeric substances as Gly, under a rich exogenous carbon supply state, and stimulated nitrogen removal by endogenous denitrifying under a scarce exogenous carbon supply state. The EDNR rate went up to 0.83 mg·(L·h)-1 in the I-A/O process, which was more than that achieved by the C-A/O process. The microbial communities in the two processes were evaluated by the Illumina HiSeq high-throughput sequencing technology. The results showed that there was no obvious difference in the sludge microbial community diversity between the two processes, but the Candidate division TM7 proliferated in the I-A/O process, and become the abundant taxa to prompt limited filamentous sludge bulking and Gly storage capability enhancement. The oxygen supply mode of AOSD made the activated sludge properties and microbial communities to be screened selectively in the new environment, aerobic heterotrophic bacterial activity to decline, and endogenous denitrifying action to strengthen, which made the I-A/O process implement a kind of dynamic balanced state that limited the DO demand.

A putative colR(XC1049)-colS(XC1050) two-component signal transduction system in Xanthomonas campestris positively regulates hrpC and hrpE operons and is involved in virulence, the hypersensitive response and tolerance to various stresses.

The ColR-ColS two-component signal transduction system was originally characterized as a regulatory system involved in the capacity of root-colonizing biocontrol bacterium Pseudomonas fluorescens to colonize plant roots. There are three pairs of putative colR-colS two-component regulatory systems annotated in the phytopathogen Xanthomonas campestris pathovar campestris. Mutational studies revealed that one of them, named colR(XC1049) and colS(XC1050), is a global regulatory system involved in various cellular processes, including virulence, hypersensitive response and stress tolerance. Growth rate determination showed that, although the colR(XC1049) and colS(XC1050) mutants are not auxotrophic, colR(XC1049) and colS(XC1050) are required for the pathogen to proliferate well in standard media and host plants. Assays of beta-glucuronidase activities of plasmid-driven promoter-gusA reporters and/or semi-quantitative RT-PCR demonstrated that colR(XC1049) and colS(XC1050) positively regulate expression of hrpC and hrpE operons, and that expression of colR(XC1049) and colS(XC1050) is not controlled by key hrp regulators HrpG and HrpX.

Comparative and functional genomics reveals genetic diversity and determinants of host specificity among reference strains and a large collection of Chinese isolates of the phytopathogen Xanthomonas campestris pv. campestris.

BACKGROUND: Xanthomonas campestris pathovar campestris (Xcc) is the causal agent of black rot disease of crucifers worldwide. The molecular genetic diversity and host specificity of Xcc are poorly understood. RESULTS: We constructed a microarray based on the complete genome sequence of Xcc strain 8004 and investigated the genetic diversity and host specificity of Xcc by array-based comparative genome hybridization analyses of 18 virulent strains. The results demonstrate that a genetic core comprising 3,405 of the 4,186 coding sequences (CDSs) spotted on the array are conserved and a flexible gene pool with 730 CDSs is absent/highly divergent (AHD). The results also revealed that 258 of the 304 proved/presumed pathogenicity genes are conserved and 46 are AHD. The conserved pathogenicity genes include mainly the genes involved in type I, II and III secretion systems, the quorum sensing system, extracellular enzymes and polysaccharide production, as well as many other proved pathogenicity genes, while the AHD CDSs contain the genes encoding type IV secretion system (T4SS) and type III-effectors. A Xcc T4SS-deletion mutant displayed the same virulence as wild type. Furthermore, three avirulence genes (avrXccC, avrXccE1 and avrBs1) were identified. avrXccC and avrXccE1 conferred avirulence on the hosts mustard cultivar Guangtou and Chinese cabbage cultivar Zhongbai-83, respectively, and avrBs1 conferred hypersensitive response on the nonhost pepper ECW10R. CONCLUSION: About 80% of the Xcc CDSs, including 258 proved/presumed pathogenicity genes, is conserved in different strains. Xcc T4SS is not involved in pathogenicity. An efficient strategy to identify avr genes determining host specificity from the AHD genes was developed.