Microbial community structure and function in response to the shift of sulfide/nitrate loading ratio during the denitrifying sulfide removal process

被引:78
|
作者
Huang, Cong [1 ]
Li, Zhi-ling [1 ]
Chen, Fan [1 ]
Liu, Qian [1 ]
Zhao, You-kang [1 ]
Zhou, Ji-zhong [3 ,4 ]
Wang, Ai-jie [1 ,2 ]
机构
[1] Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
[2] Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Key Lab Environm Biotechnol, Beijing 100085, Peoples R China
[3] Univ Oklahoma, Dept Microbiol & Plant Biol, Inst Environm Genom, Norman, OK 73019 USA
[4] Lawrence Berkeley Natl Lab, Div Earth Sci, Berkeley, CA 94270 USA
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
Denitrifying sulfide removal process; Continuous stirred tank reactor (CSTR); Sulfide/nitrate loading ratio; Microbial community structure; Function; SIMULTANEOUS BIOLOGICAL REMOVAL; SULFUR-OXIDIZING BACTERIA; THIOBACILLUS-DENITRIFICANS; ELEMENTAL SULFUR; SP-NOV; OXIDATION; REACTOR; SULFATE; NITROGEN; CARBON;
D O I
10.1016/j.biortech.2015.08.019
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Influence of acetate-C/NO3-N/S-2 ratio to the functional microbial community during the denitrifying sulfide removal process is poorly understood. Here, phylogenetic and functional bacterial community for elemental sulfur (S-0) recovery and nitrate (NO3) removal were investigated with the switched S-2 /NO3 molar ratio ranged from 5/2 to 5/9. Optimized S-2 /NO3 ratio was evaluated as 5/6, with the bacterial genera predominated with Thauera, Enterobacter, Thiobacillus and Stappia, and the sqr gene highly expressed. However, insufficient or high loading of acetate and NO3 resulted in the low S-0 recovery, and also significantly modified the bacterial community and genetic activity. With S-2 /NO3 ratio of 5/2, autotrophic S-2 oxidization genera were dominated and NO3 reduction activity was low, confirmed by the low expressed nirK gene. In contrast, S-2 /NO3 ratio switched to 5/8 and 5/9 introduced diverse heterotrophic nitrate reduction and S-0 over oxidization genera in accompanied with the highly expressed nirK and sox genes. (C) 2015 Published by Elsevier Ltd.
引用
收藏
页码:227 / 234
页数:8
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