MICROBIAL COMMUNITY ANALYSIS OF ANOXIC-OXIC-SETTLING-ANAEROBIC (A plus OSA) SLUDGE REDUCTION PROCESS USING PLFA AND PCR-DGGE METHODS

被引:0
作者
Ning, Xinqiang [1 ]
Li, Siyu [1 ]
He, Chonghao [1 ]
Liao, Yi [1 ]
Dong, Jianwei [1 ]
Gao, Xu [3 ]
Tang, Tang [2 ]
机构
[1] Sichuan Univ Sci & Engn, Coll Civil Engn, Zigong 643000, Peoples R China
[2] Sichuan Univ Sci & Engn, Coll Bioengn, Zigong 643000, Peoples R China
[3] Chongqing Water Grp Co Ltd, Chongqing 400015, Peoples R China
来源
FRESENIUS ENVIRONMENTAL BULLETIN | 2018年 / 27卷 / 11期
基金
中国国家自然科学基金;
关键词
Sludge reduction; Oxic-Settling-Anoxic (OSA) process; Microbial communities; PLFA; PCR-DGGE; PHOSPHOLIPID FATTY-ACID; GRADIENT GEL-ELECTROPHORESIS; LIPID ANALYSIS; BIOMASS; SOIL; BACTERIAL; MICROORGANISMS; FERMENTATION; EXTRACTION; DYNAMICS;
D O I
暂无
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The anoxic-oxic-settling-anaerobic (A+OSA) process, modification of the anoxic-xoic (AO) process by inserting a sludge holding tank (SHT) into the sludge return line, could achieve excess sludge reduction. The microbial communities of the A+OSA process were investigated using combined phospholipid fatty acids (PLFAs) and polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) methods. The PLFA-based microbial biomass of SHT was significantly lower (p<0.05) than that of other samples of the A+OSA process and AO process. Gram-negative (G-) bacteria and aerobe biomarkers dominated in the A+OSA and AO process except SHT in which Gram-positive (G+) bacteria and anaerobe dominated. Results of DGGE analysis suggested that 6 classes alpha-proteobacteria, beta-proteobacteria, Sphingobacteriia, Cytophagia, Ignavibacteria, Flavobacteria, were identified, and beta-proteobacteria were main microorganisms in the two processes. This study suggested that sludge decay in the SHT could be the main reason for the sludge reduction in the A+OSA process. The microgroups including alpha-proteobacteria, beta-proteobacteria and Sphingobacteria were involved in the sludge reduction.
引用
收藏
页码:7510 / 7519
页数:10
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