ライフサイエンスコーパス: Bacillus megaterium

1 riants of cytochrome P450BM3 (CYP102A1) from Bacillus megaterium.

2 that Bacillus subtilis can kill and prey on Bacillus megaterium.

3 ately 17-130-fold) than Escherichia coli and Bacillus megaterium.

4 acterial cytochrome P450 BM3 (CYP102A1) from Bacillus megaterium.

5 constructed in flavocytochrome P450 BM3 from Bacillus megaterium.

6 of the fatty acid hydroxylase P-450 BM3 from Bacillus megaterium.

7 s characteristic is similar to P450(BM-3) of Bacillus megaterium.

8 les derived from the cytoplasmic membrane of Bacillus megaterium.

9 th the beta subunit from the obligate aerobe Bacillus megaterium.

10 tial portion of its presumptive homologue in Bacillus megaterium.

11 ns and an analysis of their coding region in Bacillus megaterium 11561.

12 pecific fashion on cytochrome P450 BM-3 from Bacillus megaterium, a 119 kDa paramagnetic enzyme, usin

13 Cytochrome P450BM3 (CYP102A1) from Bacillus megaterium, a fatty acid hydroxylase, is a memb

14 rt the isolation of a spoIIGA homologue from Bacillus megaterium, a species in which the cells are si

15 nt spores of B. subtilis, Bacillus cereus or Bacillus megaterium, although germinated B. subtilis spo

16 mutants, whereas PGs from the G(+) bacteria Bacillus megaterium and Bacillus subtilis did not, sugge

17 e in the inner membrane of dormant spores of Bacillus megaterium and Bacillus subtilis is largely imm

18 rminant receptors (GRs) in dormant spores of Bacillus megaterium and Bacillus subtilis species have s

19 fficiently triggered germination of decoated Bacillus megaterium and Bacillus subtilis spores lacking

20 Spores of Bacillus megaterium and Bacillus subtilis strains were h

21 ar to those of citrate synthase enzymes from Bacillus megaterium and from eukaryotic cells but differ

22 bstrate binding to cytochrome P-450 BM3 from Bacillus megaterium and its constituent haem-containing

23 cterial isolates as food, we identified two, Bacillus megaterium and Pseudomonas mendocina, that enha

24 anaerobic cobalamin biosynthetic pathway in Bacillus megaterium and using homologously overproduced

25 Here we report structures of the Bacillus megaterium apoCcpA and a CcpA-(HPr-Ser46-P)-DNA

26 e report the crystal structure of P(46) from Bacillus megaterium at 3.0 A resolution and the fact tha

27 ns, Bacillus cereus, Bacillus licheniformis, Bacillus megaterium, Bacillus subtilis (including Bacill

28 Among 12 microorganisms tested, Bacillus megaterium, Bacillus subtilis, Staphyloccocus a

29 provide evidence of nutrient extraction from Bacillus megaterium by Bacillus subtilis.

30 that Bacillus subtilis can kill and prey on Bacillus megaterium by delivering a toxin and extracting

31 The Bacillus megaterium cbiF, encoding the cobalt-precorrin-

32 f monosaccharide substrates using engineered Bacillus megaterium cytochrome P450 (P450(BM3)) demethyl

33 tween the heme and FMN-containing domains of Bacillus megaterium cytochrome P450BM-3 indicates that t

34 rming bacteria such as Bacillus subtilis and Bacillus megaterium for development of luminescent sensi

35 We also show that TubR from Bacillus megaterium forms a helical superstructure resem

36 of OXT-A has been linked to a plasmid-borne Bacillus megaterium gene cluster that contains four gene

37 ally essential amino acids by mutagenesis of Bacillus megaterium gpr.

38 find that Bacillus subtilis rapidly inhibits Bacillus megaterium growth by delivering the tRNase toxi

39 The Gram-positive aerobic bacterium Bacillus megaterium has a complete anaerobic pathway tha

40 Wild-type CYP102 (P450(BM-3)) from Bacillus megaterium has low activity for the oxidation o

41 3) (CYP102A1), a fatty acid hydroxylase from Bacillus megaterium, has been extensively studied over a

42 ures and biochemical characterization of the Bacillus megaterium HD domain phosphohydrolase OxsA, inv

43 The germination protease (GPR) of Bacillus megaterium initiates the degradation of small,

44 P450BM-3 from Bacillus megaterium is a widely studied P450 cytochrome

45 Bacillus megaterium is deep-rooted in the Bacillus phylo

46 102A1, a widely studied cytochrome P450 from Bacillus megaterium, is capable of very efficient oxidat

47 Four of the six isolates were identified as Bacillus megaterium, one was identified as Bacillus cere

48 Purification of either recombinant Bacillus megaterium or Synechocystis CbiXL in Escherichi

49 The Bacillus megaterium P450 BM3 enzyme is a key model syste

50 residues of the cytochrome P450 enzyme from Bacillus megaterium (P450-BM3), a highly active His-liga

51 Spores of Bacillus megaterium QM B1551 germinate in response to a

52 glucose as a germinant molecule by spores of Bacillus megaterium QM B1551 has been examined.

53 om the approximately 53 kb pBM400 plasmid of Bacillus megaterium QM B1551 has been sequenced and char

54 plied to examine the function in vivo of the Bacillus megaterium QM B1551 SleB and SleL proteins.

55 for differences in germinant recognition of Bacillus megaterium QM B1551 spores containing the GerVB

56 This novel PHA synthase from Bacillus megaterium required PhaC (PhaC(Bm)) and PhaR (P

57 Here, we show that a soil bacterial isolate, Bacillus megaterium Sb5, promotes plant infection by Phy

58 r aspect of the membrane, that influence the Bacillus megaterium spore germination response.

59 to permeabilize the cytoplasmic membrane of Bacillus megaterium than theromacin and hydramacin-1.

60 Stage I germinated spores of Bacillus megaterium that had slightly increased core wat

61 In SASP-A and SASP-C of Bacillus megaterium two conserved glutamate residues, wh

62 Tyrosinase from Bacillus megaterium (TyrBm) was previously used to modul

63 ts of R. solanacearum, R. metallidurans, and Bacillus megaterium using chemical tests, a siderophore

64 fficient soluble fatty acid hydroxylase from Bacillus megaterium utilizing tightly bound FAD and FMN

65 of 15 putative gas vesicle genes (gvp) from Bacillus megaterium VT1660 and their functional expressi

66 Cytochrome P450 BM-3 from Bacillus megaterium was engineered using a combination o

67 A Gram-positive spore former (Bacillus megaterium) was distinguished by an abundant pe

68 Superdormant spores of Bacillus subtilis and Bacillus megaterium were isolated in 4 to 12% yields fol

69 majority of spores of Bacillus subtilis and Bacillus megaterium were ring shaped.

70 ch features to the corresponding sequence in Bacillus megaterium, which reflects the consensus sequen