Diversity of Pseudomonas strains isolated with King's B and Gould's S1 agar determined by repetitive extragenic palindromic polymerase chain reaction, 16S rDNA sequencing and Fourier transform infrared spectroscopy characterisation

被引:46
作者
Johnsen, K
Nielsen, P
机构
[1] Geol Survey Denmark & Greenland, DK-2400 Copenhagen NV, Denmark
[2] Novo Nordisk AS, Enzyme Res, DK-2880 Bagsvaerd, Denmark
[3] Royal Vet & Agr Univ, Dept Ecol, Genet & Microbiol Sect, Copenhagen, Denmark
关键词
Pseudomonas; Fourier transform infrared spectroscopy; Gould's S1; King's B; characterization;
D O I
10.1111/j.1574-6968.1999.tb13497.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
King's B and Gould's S1 agar were compared with regard to the isolation of Pseudomonas from four environmental samples. In all samples, King's B gave the highest number of colony-forming units, and in some environments, there were more fluorescent colony-forming units on King's B as well. However, almost all types grew on Gould's S1, which enabled us to isolate a greater variety of groups than with King's B, fluorescent as well as non-fluorescent members of Pseudomonas. The Pseudomonas isolates were comparatively typed by repetitive extragenic palindromic-polymerase chain reaction and Fourier transform infrared spectroscopy, not previously used for environmental Pseudomonas. The two typing methods were similar in resolution, thus Fourier transform infrared spectroscopy proved fast and reproducible and is a good method for discrimination at subspecies level. Representative strains were identified by partial 16S rDNA sequencing. Thus, we suggest Gould's S1 agar be used for isolation of Pseudomonas because the results are reproducible, specific and give the most diverse recovery and the least work. (C) 1999 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:155 / 162
页数:8
相关论文
共 24 条
[1]   The phylogeny of the genera Chryseomonas, Flavimonas, and Pseudomonas supports synonymy of these three genera [J].
Anzai, Y ;
Kudo, Y ;
Oyaizu, H .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1997, 47 (02) :249-251
[2]  
BALKWILL DL, 1990, ISOLATION BIOTECHNOL, P183
[3]   16S rRNA gene sequence analysis relative to genomovars of Pseudomonas stutzeri and proposal of Pseudomonas balearica sp nov [J].
Bennasar, A ;
RosselloMora, R ;
Lalucat, J ;
Moore, ERB .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1996, 46 (01) :200-205
[4]   USE OF REPETITIVE (REPETITIVE EXTRAGENIC PALINDROMIC AND ENTEROBACTERIAL REPETITIVE INTERGENERIC CONSENSUS) SEQUENCES AND THE POLYMERASE CHAIN-REACTION TO FINGERPRINT THE GENOMES OF RHIZOBIUM-MELILOTI ISOLATES AND OTHER SOIL BACTERIA [J].
DEBRUIJN, FJ .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1992, 58 (07) :2180-2187
[5]   NEW SELECTIVE MEDIA FOR ENUMERATION AND RECOVERY OF FLUORESCENT PSEUDOMONADS FROM VARIOUS HABITATS [J].
GOULD, WD ;
HAGEDORN, C ;
BARDINELLI, TR ;
ZABLOTOWICZ, RM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1985, 49 (01) :28-32
[6]   MEDIUM FOR SELECTIVE ISOLATION OF MEMBERS OF GENUS PSEUDOMONAS FROM NATURAL HABITATS [J].
GRANT, MA ;
HOLT, JG .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1977, 33 (05) :1222-1224
[7]  
Harayama S., 1989, Genetics of bacterial diversity., P151
[8]   PSEUDOMONAS FLAVESCENS SP-NOV, ISOLATED FROM WALNUT BLIGHT CANKERS [J].
HILDEBRAND, DC ;
PALLERONI, NJ ;
HENDSON, M ;
TOTH, J ;
JOHNSON, JL .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1994, 44 (03) :410-415
[9]   Phenotypic and genotypic characterization of phenanthrene degrading fluorescent Pseudomonas biovars [J].
Johnsen, K ;
Andersen, S ;
Jacobsen, CS .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (10) :3818-3825
[10]  
JUKES T H, 1969, P21