The ldh phylogeny for environmental isolates of Lactococcus lactis is consistent with rRNA genotypes but not with phenotypes

被引:30
作者
Urbach, E
Daniels, B
Salama, MS
Sandine, WE
Giovannoni, SJ
机构
关键词
D O I
10.1128/AEM.63.2.694-702.1997
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
Lactate dehydrogenase (Idh) gene sequences, levels of 16S rRNA group-specific probe binding, and phenotypic characteristics were compared for 45 environmental isolates and four commercial starter strains of Lactococcus lactis to identify evolutionary groups best suited to cheddar cheese manufacture. Idh sequences from the environmental isolates showed high similarity to those from two groups oft. lactis used for industrial fermentations, L. lactis subsp. cremoris and subsp. lactis. Within each phylogenetically defined subspecies, [ldh sequence similarities were greater than 99.1%. Strains with phenotypic traits formerly diagnostic for both subspecies were found in each Idh similarity group, but only strains belonging to L. lactis subsp. cremoris by both the newer, genetic and the older, superseded phenotypic criteria were judged potentially suitable for the commercial production of cheddar cheese. Identical evolutionary relationships were inferred from Idh sequences and from binding of subspecies-specific, 16S rRNA-directed oligonucleotide probes. However, groups defined according to these chromosomal traits bore no relationship to patterns of arginine deamination, carbon substrate utilization, or bacteriophage sensitivity, which may be encoded by cryptic genes or sexually transmissible genetic elements. Fourteen new L. lactis subsp. cremoris isolates were identified as suitable candidates for cheddar cheese manufacture, and 10 of these were completely resistant to three different batteries of commercial bacteriophages known to reduce starter activity.
引用
收藏
页码:694 / 702
页数:9
相关论文
共 41 条
[1]   LACTOCOCCUS GENUS - A SELECTIVE AND DIFFERENTIAL AGAR MEDIUM [J].
ALZOREKY, N ;
SANDINE, WE .
JOURNAL OF FOOD SCIENCE, 1991, 56 (06) :1729-&
[2]  
ALZOREKY N, 1991, J FOOD SCI, V56, P1734
[3]  
DANIELS B, UNPUB
[4]   APPEARANCE OF THE ARGININE PHENOTYPE IN LACTOCOCCUS-LACTIS SUBSP CREMORIS 2204 FOLLOWING PHAGE TRANSDUCTION [J].
DAVEY, GP ;
HEAP, HA .
CANADIAN JOURNAL OF MICROBIOLOGY, 1993, 39 (08) :754-758
[5]   A SEQUENCE ASSEMBLY AND EDITING PROGRAM FOR EFFICIENT MANAGEMENT OF LARGE PROJECTS [J].
DEAR, S ;
STADEN, R .
NUCLEIC ACIDS RESEARCH, 1991, 19 (14) :3907-3911
[6]   MOSAIC STRUCTURE OF LARGE REGIONS OF THE LACTOCOCCUS-LACTIS SUBSP CREMORIS CHROMOSOME [J].
DELORME, C ;
GODON, JJ ;
EHRLICH, SD ;
RENAULT, P .
MICROBIOLOGY-SGM, 1994, 140 :3053-3060
[7]   THERMOSENSITIVE PLASMID REPLICATION, TEMPERATURE-SENSITIVE HOST GROWTH, AND CHROMOSOMAL PLASMID INTEGRATION CONFERRED BY LACTOCOCCUS-LACTIS SUBSP CREMORIS LACTOSE PLASMIDS IN LACTOCOCCUS-LACTIS SUBSP LACTIS [J].
FEIRTAG, JM ;
PETZEL, JP ;
PASALODOS, E ;
BALDWIN, KA ;
MCKAY, LL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1991, 57 (02) :539-548
[8]  
Felsenstein J., 1993, PHYLIP
[9]   STREPTOCOCCUS-LACTIS SUBSP CREMORIS (ORLA-JENSEN) COMB-NOV AND STREPTOCOCCUS-LACTIS SUBSP DIACETILACTIS (MATUSZEWSKI ET AL) NOM-REV, COMB-NOV [J].
GARVIE, EI ;
FARROW, JAE .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1982, 32 (04) :453-455
[10]  
Giovannoni S., 1991, NUCL ACID TECHNIQUES, P177