[1] Amann RI, Ludwig W, Schleifer KH. 1995. Phylogenetic identificationand in situ detection of individual microbial cells without cultivation.Microbiol Reviews, 5 9 (1):143~169 [2] Ausubel FM, Brent R, Kingston RE et al. 1995. Short Protocols inMolecular Biology. 3rd ed. New York:John Wiley & Sons, Inc. [3] Borneman J, Triplett EW. 1997. Molecular microbial diversity in soilsfrom Eastern Amazonia:Evidence for unusual microorganisms and mi-crobial population shifts associated with deforestation. Appl EnvironMicrobiol, 63 (7):2647~2653 [4] Braker G, Fesefeldt A, Witzel KP. 1998. Development of PCR primersystems for amplification of nitrite reductase genes (nirK and nirS)to detect denitrifying bacteria in environmental samples. Appl EnvironMicrobiol, 64(10):3769~3775 [5] Britschgi TB, Giovannoni S. 1991. Analysis of a natural marine bacterioplankton population by rRNA cloning, sequencing. Appl Environ Mi crobiol, 57:1707~1713 [6] Brunel B, Givaudan A, Lanois A et al. 1997. Fast, accurate identification of Xenorhabdus and Photorhabdus species by restriction analysisof PCR-amplified 16S rRNA genes. Appl Environ Microbiol, 63(2):574~580 [7] Cotthew MT, Cary SC. 1999. Diversity of dissimilatory bisulfite reductase genes of bacteria associated with the deep-sea hydrothermal ventpolychaete annelid Alvinella pompejana. Appl Environ Microbiol, 65(3):1127~1132 [8] de Peer YV, Jansen J, de Rijk P et al. 1997. Database on the structureof small ibosomal subunit RNA. Nucl Acid Res, 25(1):111~116 [9] Fantrousi SE, Verschuere L, Verstraete W et al. 1999. Effect ofphenylurea herbicides on soil microbial communities estimated by analysis of 16S rRNA gene fingerprints, community level physiological profiles. Appl Environ Microbiol, 65 (3):982~988 [10] Felske A, Wolterink A, Vanlis R et al. 1998. Phylogeny of the mainbacterial 16S rRNA sequences in Drentse A grassland soils (TheNetherlands). Appl Environ Microbiol, 64(3):871~879 [11] Field KG, Gordon D, Wright T et al. 1997. Diversity, depth-specificdistribution of SAR1 1 cluster rRNA genes from marine planktonic bacteria. Appl Environ Microbiol, 63 (1):63~70 [12] Fisher MM, Wilcox LW, Graham LE. 1998. Molecular characterizationof epiphytic bacterial communities on charophycean green algae. ApplEnviron Microbiol, 64(11):4384~4389 [13] Hiorns WD, Methe BA, Nierzwicki-Bauer SA et al. 1997. Bacterial diversity, Adirondack mountain lakes as determined by 16S rRNA genesequences. Appl Environ Microbiol, 63(7):2957~2960 [14] Huys G, Coopman R, Janssen P et al. 1996. High-resolution genotypicanalysis of the genus Aerornonas by AFLP fingerprinting. Intern JSyst Bact, 46 (2):572~580 [15] Kuske CK, Barns SM, Busch JD. 1997. Diverse uncultivated groupfrom soils of the arid southwestern United States that are present inmany geographic regions. Appl Environ Microbiol, 63 (9):3614~3621 [16] Nanjing Soil Institute, Chinese Academy of Sciences(中国科学院南京土壤研究所)1983. Physical, Chemical Analysis of Soil. Shanghai:Shanghai Science and Technology Press. 68~72,132~136 (in Chinese) [17] Nielsen AT, Liu WT, Filipe C et al. 1999. Identification of a novelgroup of bacteria in sludge from a deteriorated biological phosphorusremoval reactor. Appl Environ Microbiol, 65(3):1251~1258 [18] Rasmussen U, Svenning M. 1998. Figerprinting of cyanobacteria basedon PCR with primers derived from short, long tandemly repeatedrepetitive sequences. Appl Environ Microbiol, 64(1):265~272 [19] Southern EM. 1979. Measurement of DNA length by gel electrophore sis. Anal Biochem, 100:319~323 [20] Stephen JR, Chang YJ, Macnaughton SJ et al. 1999. Effect of toxicmetals on indigenous soil β-subgroup proteobacterium ammonia oxidizercommunity structure, protection against toxity by inoculated metal-re-sistant bacteria. Appl Environ Microbiol, 65(1):95~101 [21] van Steenbergen TJM, Colloms SD, Hermans PW et al. 1995. GenomicDNA figerprinting by restriction fragment end labeling. Proc Natl Acad Sci USA, 92:5572~5576 [22] Wawer C, Jetten MSM. and Muyzer G. 1998. Genetic diversity, expression of the [ NiFe] hydrogenase large-subunit gene of Desulfovibriospp. in environmental samples. Appl Environ Microbiol, 64 (11):4360~4369 [23] Wagner M, Roger AJ, Flax JL et al. 1998. Phylogeny of dissimilatorysulfite reductases supports an early origin of sulfate respiration. JBact,180(11):2975~2982 [24] Wang FR, Cao WW, Campbell WL et al. 1994. The use of PCR tomonitor the population abundance of six human intestinal bacterialspecies in an in vitro semicontinuous culture system. FEMS MicrobiolLetters, 124:229~238 [25] Widmer F, Shaffer BT, Porteous LA et al. 1999. Analysis of nifH genepool complexity in soil, litter at a Douglas fir forest site in the OregonCascade Mountain Range. Appl Environ Microbiol, 65 (2):374~380 [26] YangG-P(杨官品),ZhuY-H(朱艳红),Li Z-G(李志岗).1998.Direct cloning of bacterial genes from soil:16S ribosomal RNA gene as amodel.JHubei Univ(湖北大学学报),4:383~385(in Chinese) |