Microbial succession during a composting process as evaluated by denaturing gradient gel electrophoresis analysis

被引:196
作者
Ishii, K [1 ]
Fukui, M [1 ]
Takii, S [1 ]
机构
[1] Tokyo Metropolitan Univ, Grad Sch Sci, Dept Biol Sci, Tokyo 1920397, Japan
关键词
D O I
10.1046/j.1365-2672.2000.01177.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Microbial succession during a laboratory-scale composting process of garbage was analysed by denaturing gradient gel electrophoresis (DGGE) combined with measurement of physicochemical parameters such as temperature, pH, organic acids, total dissolved organic carbon and water-soluble humic substance. From the temperature changes, a rapid increase from 25 to 58 degreesC and then a gradual decrease, four phases were recognized in the process as follows; mesophilic (S), thermophilic (T), cooling (C) and maturing (M). The polymerase chain reaction-amplified 16S rDNA fragments with universal (907R) and eubacterial (341F with GC clamp) primers were subjected to DGGE analysis. Consequently, the DGGE band pattern changed during the composting process. The direct sequences from DGGE bands were related to those of known genera in the DNA database. The microbial succession determined by DGGE was summarized as follows: in the S phase some fermenting bacteria, such as lactobacillus, were present with the existing organic acids; in the T phase thermophilic bacillus appeared and, after the C phase, bacterial populations were more complex than in previous phases and the phylogenetic positions of those populations were relatively distant from strains so far in the DNA database. Thus, the DGGE method is useful to reveal microbial succession during a composting process.
引用
收藏
页码:768 / 777
页数:10
相关论文
共 38 条
[1]   PHYLOGENETIC IDENTIFICATION AND IN-SITU DETECTION OF INDIVIDUAL MICROBIAL-CELLS WITHOUT CULTIVATION [J].
AMANN, RI ;
LUDWIG, W ;
SCHLEIFER, KH .
MICROBIOLOGICAL REVIEWS, 1995, 59 (01) :143-169
[2]  
Carpenter-Boggs L, 1998, APPL ENVIRON MICROB, V64, P4062
[3]   THE PHYLOGENY OF THE GENUS CLOSTRIDIUM - PROPOSAL OF 5 NEW GENERA AND 11 NEW SPECIES COMBINATIONS [J].
COLLINS, MD ;
LAWSON, PA ;
WILLEMS, A ;
CORDOBA, JJ ;
FERNANDEZGARAYZABAL, J ;
GARCIA, P ;
CAI, J ;
HIPPE, H ;
FARROW, JAE .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1994, 44 (04) :812-826
[4]   EFFECT OF GENOME SIZE AND RRN GENE COPY NUMBER ON PCR AMPLIFICATION OF 16S RIBOSOMAL-RNA GENES FROM A MIXTURE OF BACTERIAL SPECIES [J].
FARRELLY, V ;
RAINEY, FA ;
STACKEBRANDT, E .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1995, 61 (07) :2798-2801
[5]   Population structure and physiological changes within a hot spring microbial mat community following disturbance [J].
Ferris, MJ ;
Nold, SC ;
Revsbech, NP ;
Ward, DM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (04) :1367-1374
[6]  
Finstein M S, 1975, Adv Appl Microbiol, V19, P113, DOI 10.1016/S0065-2164(08)70427-1
[7]  
FORSYTH WGC, 1948, P SOC APPL BACTERIOL, V11, P34
[8]   HOW CLOSE IS CLOSE - 16S RIBOSOMAL-RNA SEQUENCE IDENTITY MAY NOT BE SUFFICIENT TO GUARANTEE SPECIES IDENTITY [J].
FOX, GE ;
WISOTZKEY, JD ;
JURTSHUK, P .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1992, 42 (01) :166-170
[9]   EVOLUTION OF ENZYME-ACTIVITIES AND MICROBIAL-POPULATIONS DURING COMPOSTING OF CATTLE MANURE [J].
GODDEN, B ;
PENNINCKX, M ;
PIERARD, A ;
LANNOYE, R .
EUROPEAN JOURNAL OF APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1983, 17 (05) :306-310
[10]  
GOLUEKE CG, 1954, APPL MICROBIOLOGY, V2, P44