BIOCHEMICAL-CHARACTERIZATION OF LACTOCOCCUS-LACTIS IO-1 WHOSE OPTIMAL TEMPERATURE IS AS HIGH AS 37-DEGREES-C

被引:47
作者
ISHIZAKI, A
OSAJIMA, K
NAKAMURA, K
KIMURA, K
HARA, T
EZAKI, T
机构
[1] KYUSHU UNIV, FAC AGR, INST GENET RESOURCES, HIGASHI KU, FUKUOKA 812, JAPAN
[2] GIFU UNIV, SCH MED, DEPT MICROBIOL, GIFU 500, JAPAN
关键词
D O I
10.2323/jgam.36.1
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
An L-lactate producing strain whose optimal temperature for growth and L-lactate production was 37°C, previously labeled as Streptococcus species I0-1 was characterized biochemically and genetically and identified as a variant strain of Lactococcus lactis. This strain tolerated 6.5% NaCl and grew on bile esculin agar. Thus the strain resembled enterococci biochemically. However, there was no Lancefield’s group D antigen in the strain, but group N antigen was present. Quantitative DNA-DNA hybridization experiments showed that the strain did not resemble enterococci and should be assigned to the genus Lactococcus. Strain I0-1 was identified as a strain of Lactococcus lactis because the homology values between it and the type strain of the L. lactis, NCFB 604T were in a range of 62-77%. The growth of L. lactis is usually suppressed and very slow at 42°C but strain I0-1 grew confluently and very quickly at that temperature. It was also different from the type strain of L. lactis in that it produced antibiotics, which were not nisin but were similar to nisin to which other lactococci and some species of genus Bacillus and Clostridium were sensitive. This strain has been deposited in the Japan Collection of Microorganisms as L. lactis 10-1 JCM 7638. © 1990, Applied Microbiology, Molecular and Cellular Biosciences Research Foundation. All rights reserved.
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页码:1 / 6
页数:6
相关论文
共 19 条
[1]   INFLUENCE OF PH, LACTOSE AND LACTIC-ACID ON THE GROWTH OF STREPTOCOCCUS-CREMORIS - A KINETIC-STUDY [J].
BIBAL, B ;
GOMA, G ;
VAYSSIER, Y ;
PAREILLEUX, A .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1988, 28 (4-5) :340-344
[2]   SIMPLE GENETIC METHOD TO IDENTIFY VIRIDANS GROUP STREPTOCOCCI BY COLORIMETRIC DOT HYBRIDIZATION AND FLUOROMETRIC HYBRIDIZATION IN MICRODILUTION WELLS [J].
EZAKI, T ;
HASHIMOTO, Y ;
TAKEUCHI, N ;
YAMAMOTO, H ;
LIU, SL ;
MIURA, H ;
MATSUI, K ;
YABUUCHI, E .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (09) :1708-1713
[3]   FLUOROMETRIC DEOXYRIBONUCLEIC ACID DEOXYRIBONUCLEIC ACID HYBRIDIZATION IN MICRODILUTION WELLS AS AN ALTERNATIVE TO MEMBRANE-FILTER HYBRIDIZATION IN WHICH RADIOISOTOPES ARE USED TO DETERMINE GENETIC RELATEDNESS AMONG BACTERIAL STRAINS [J].
EZAKI, T ;
HASHIMOTO, Y ;
YABUUCHI, E .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1989, 39 (03) :224-229
[4]  
Facklam RR, 1985, MANUAL CLIN MICROBIO, V4th, P154
[5]  
Hurst A, 1981, NISIN ADV APPL MICRO, V27, P85, DOI [10.1016/S0065-2164(08)70342-3, DOI 10.1016/S0065-2164(08)70342-3]
[6]   BATCH CULTURE KINETICS OF L-LACTATE FERMENTATION EMPLOYING STREPTOCOCCUS SP IO-1 [J].
ISHIZAKI, A ;
OHTA, T .
JOURNAL OF FERMENTATION AND BIOENGINEERING, 1989, 67 (01) :46-51
[7]  
JORGENSEN MH, 1987, APPL MICROBIOL BIOT, V25, P313, DOI 10.1007/BF00252539
[8]   DETERMINATION OF THE NUCLEOTIDE COMPOSITION OF A DEOXYRIBONUCLEIC-ACID BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY OF ITS ENZYMATIC HYDROLYSATE - A REVIEW [J].
KANEKO, T ;
KATOH, K ;
FUJIMOTO, M ;
KUMAGAI, M ;
TAMAOKA, J ;
KATAYAMAFUJIMURA, Y .
JOURNAL OF MICROBIOLOGICAL METHODS, 1986, 4 (5-6) :229-240
[9]  
Kitahara K, 1957, J GEN APPL MICROBIOL, V3, P102, DOI DOI 10.2323/JGAM.3.102
[10]  
Kitara K, 1957, J GEN APPL MICROBIOL, V3, P111, DOI DOI 10.2323/JGAM.3.111