2012
Enterococcus rivorum sp. nov., from water of pristine brooks
NIEMI, Maarit R., Tuula OLLINKANGAS, Lars PAULIN, Pavel ŠVEC, Peter VANDAMME et. al.Základní údaje
Originální název
Enterococcus rivorum sp. nov., from water of pristine brooks
Autoři
NIEMI, Maarit R. (246 Finsko), Tuula OLLINKANGAS (246 Finsko), Lars PAULIN (246 Finsko), Pavel ŠVEC (203 Česká republika, garant, domácí), Peter VANDAMME (56 Belgie), Antti KARKMAN (246 Finsko), Marcel KOSINA (203 Česká republika, domácí) a Kristina LINDSTROM (246 Finsko)
Vydání
International Journal of Systematic and Evolutionary Microbiology, UK, Society for General Microbiology, 2012, 1466-5026
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10600 1.6 Biological sciences
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.112
Kód RIV
RIV/00216224:14310/12:00061421
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000310048600020
Klíčová slova anglicky
Enterococcus rivorum sp. nov.; pristine brooks; taxonomy
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 9. 4. 2013 21:31, Ing. Andrea Mikešková
Anotace
V originále
A significant number of Enterococcus strains from pristine waters of two brooks in Finland formed a distinct cluster on the basis of whole-cell protein fingerprinting by one-dimensional SDS-PAGE. The strains shared the following characteristics. Cells were ovoid, Gram-positive-staining and non-spore-forming, appearing singly or in pairs or chains. They were facultatively anaerobic and catalase-negative. Growth in broth containing 6.5% NaCl or at 45 6C was weak or absent. Production of D antigen was variable. The strains tolerated 60 6C for 30 min, 40% bile and tellurite, hydrolysed aesculin strongly and gelatin weakly, produced no acid from hippurate and did not reduce it, grew weakly at 10 6C, showed a strong reaction for the Voges–Proskauer test and produced acid from methyl a-D-glucoside, mannitol, sorbitol and sucrose, with weak or no production of acid from methyl a-D-mannoside, L-arabinose, gluconate and L-xylose. Several of the strains were selected for identification on the basis of sequencing of almost the whole 16S rRNA gene and partial atpA and pheS genes and of (GTG)5-PCR fingerprints. Partial atpA and pheS gene sequencing was also performed for those type strains of Enterococcus species without available sequences in the database. The pristine brook isolates formed a novel species, for which the name Enterococcus rivorum sp. nov. (type strain S299T =HAMBI 3055T =LMG 25899T 5CCM 7986T) is proposed. On the basis of 16S rRNA gene sequence similarity, E. rivorum sp. nov. is related to the Enterococcus faecalis genogoup. It is distinguished from described Enterococcus species on the basis of 16S rRNA, atpA and pheS gene sequences and whole-cell protein and (GTG)5-PCR fingerprints. It is most closely related to E. faecalis, but DNA–DNA hybridization confirms it to represent a novel species.
Návaznosti
MSM0021622416, záměr |
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