ライフサイエンスコーパス: fermentans

1 e expressed in propagating populations of M. fermentans.

2 ritis, only one of whom was infected with M. fermentans.

3 gdorferi, Treponema pallidum, and Mycoplasma fermentans.

4 against part of the two 16S rRNA genes of M. fermentans.

5 activating lipopeptide, on the surface of M. fermentans.

6 Pelosinus fermentans 16S rRNA gene sequences have been reported fr

7 kb Ureaplasma urealyticum, 1.2-Mb Mycoplasma fermentans, 2.3-Mb Streptococcus pneumoniae, and 4.6-Mb

8 riation is shown here to occur in Mycoplasma fermentans, a chronic human infectious agent and possibl

9 gdorferi, Treponema pallidum, and Mycoplasma fermentans activated cells heterologously expressing TLR

10 1 control subjects were also positive for M. fermentans and M. genitalium by PCR.

11 tans, binds human HeLa cells and inhibits M. fermentans binding to these cells, in both a quantitativ

12 undant P29 surface lipoprotein of Mycoplasma fermentans, binds human HeLa cells and inhibits M. ferme

13 re with the incognitus and PG18 strains of M fermentans, but surprisingly not with some other strains

14 CoA dehydrogenase (Bcd) from Acidaminococcus fermentans catalyze the endergonic reduction of ferredox

15 kunkelii, Mycoplasma pulmonis and Mycoplasma fermentans cluster together and are more similar to TraE

16 e MALP-404 surface lipoprotein of Mycoplasma fermentans comprises a membrane-anchored N-terminal lipi

17 Membrane preparations of A. fermentans contain a highly active ferredoxin/flavodoxin

18 Acidaminococcus fermentans degrades glutamate via the hydroxyglutarate p

19 ome sequence reported here suggested that D. fermentans employs membrane-bound hydrogenases and novel

20 In eight isolates of M. fermentans examined, malp occurred upstream of an operon

21 onspicua produced white colonies; the Pichia fermentans group and C. krusei did not.

22 Mycoplasma fermentans had previously been isolated from patients wi

23 Since 1970 Mycoplasma fermentans has been suspected of being associated with r

24 ermentans incognitus and other strains of M. fermentans have been associated with rheumatoid arthriti

25 M. fermentans incognitus alone induced an incomplete arrest

26 M. fermentans incognitus and other strains of M. fermentans

27 While cell extracts of M. fermentans incognitus can induce changes in murine and h

28 Mycoplasma fermentans incognitus has been isolated from human tissu

29 inflammation, we examined the effects of M. fermentans incognitus on surface markers and functions o

30 M. fermentans incognitus only minimally affected changes in

31 posed to phorbol myristate acetate (PMA), M. fermentans incognitus, or both.

32 We examined effects of Mycoplasma fermentans infection on the continuing survival and immo

33 e the movement of a previously identified M. fermentans insertion sequence (IS)-like element.

34 A new insertion sequence (IS) of Mycoplasma fermentans is described.

35 t of succinic, oxalic and acetic acids by P. fermentans is reported for the first time in this work,

36 The malp gene of Mycoplasma fermentans is shown to occur in single copy but to encod

37 Desulfurococcus fermentans is the first known cellulolytic archaeon.

38 ed sites of chromosomal integration among M. fermentans isolates suggest a role for ICEF in promoting

39 Pelosinus fermentans JBW45 is an anaerobic, lactate-fermenting bac

40 y dramatically in ratio among isolates of M. fermentans occur on the mycoplasma surface: (i) MALP-404

41 In comparison, live Mycoplasma fermentans or M. penetrans infection for 4 to 5 weeks in

42 <5 copies of Mycoplasma hominis, Mycoplasma fermentans, or a molecular mimic control in synovial flu

43 is present in four copies in the Mycoplasma fermentans PG18 chromosome, accounting for approximately

44 approximately 16 kb genome of the Mycoplasma fermentans phiMFV1 prophage is described, and its mobili

45 we show that recombinant flavodoxin from A. fermentans produced in Escherichia coli can replace ferr

46 nted in a series of clonal derivatives of M. fermentans propagated in culture.

47 ed ICEF (integrative conjugal elements of M. fermentans), resemble conjugative, self-transmissible in

48 lipid-modified surface protein of Mycoplasma fermentans, reveal phase variation of surface epitopes o

49 In various M. fermentans strains, phiMFV1 was either absent or integra

50 re present in the genomes of at least two M. fermentans strains.

51 ween the expression of a specific Mycoplasma fermentans surface antigen (Pra, proteinase-resistant an

52 We present the genome sequence of the P. fermentans type strain R7 (DSM 17108) and genome sequenc

53 M. fermentans was detected in 23 of 26 (88%) rheumatoid art

54 The distribution of M. fermentans was studied in the synovial fluid of patients

55 M. fermentans was therefore found to be a variable and very

56 t and the cellulolytic bacterium Actinotalea fermentans, we are able to achieve methyl halide product

57 CoA dehydrogenase (BcdAf) of Acidaminococcus fermentans, which couple the exergonic reduction of crot

58 e 5.8S internal transcribed spacer as Pichia fermentans, Wickerhamomyces anomalus and Candida oleophi

59 ts suggest that the direct interaction of M. fermentans with a ligand on the HeLa cell surface involv