ライフサイエンスコーパス: megaterium

1 ion of its presumptive homologue in Bacillus megaterium.

2 cytochrome P450BM3 (CYP102A1) from Bacillus megaterium.

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

4 cytochrome P450 BM3 (CYP102A1) from Bacillus megaterium.

5 illus subtilis can kill and prey on Bacillus megaterium.

6 he first rRNA operon to be sequenced from B. megaterium.

7 ed in flavocytochrome P450 BM3 from Bacillus megaterium.

8 tty acid hydroxylase P-450 BM3 from Bacillus megaterium.

9 eristic is similar to P450(BM-3) of Bacillus megaterium.

10 ed from the cytoplasmic membrane of Bacillus megaterium.

11 ta subunit from the obligate aerobe Bacillus megaterium.

12 A accumulation, as observed previously in B. megaterium.

13 analysis of their coding region in Bacillus megaterium 11561.

14 ashion on cytochrome P450 BM-3 from Bacillus megaterium, a 119 kDa paramagnetic enzyme, using solid-s

15 Cytochrome P450BM3 (CYP102A1) from Bacillus megaterium, a fatty acid hydroxylase, is a member of a v

16 olation of a spoIIGA homologue from Bacillus megaterium, a species in which the cells are significant

17 of B. subtilis, Bacillus cereus or Bacillus megaterium, although germinated B. subtilis spores were

18 whereas PGs from the G(+) bacteria Bacillus megaterium and Bacillus subtilis did not, suggesting tha

19 inner membrane of dormant spores of Bacillus megaterium and Bacillus subtilis is largely immobile, as

20 eceptors (GRs) in dormant spores of Bacillus megaterium and Bacillus subtilis species have small open

21 y triggered germination of decoated Bacillus megaterium and Bacillus subtilis spores lacking endogeno

22 Spores of Bacillus megaterium and Bacillus subtilis strains were harvested

23 In Bacillus megaterium and Bacillus subtilis, energization of cytopl

24 ucose, glycerol, or acetate compared with B. megaterium and E. coli.

25 se of citrate synthase enzymes from Bacillus megaterium and from eukaryotic cells but differed from t

26 inding to cytochrome P-450 BM3 from Bacillus megaterium and its constituent haem-containing and flavi

27 solates as food, we identified two, Bacillus megaterium and Pseudomonas mendocina, that enhanced resi

28 to be determined for the CbiXL from both B. megaterium and Synechocystis.

29 c cobalamin biosynthetic pathway in Bacillus megaterium and using homologously overproduced enzymes,

30 d superdormant spores of Bacillus cereus, B. megaterium, and B. subtilis isolated after optimal heat

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

32 layer orders inferred for B. subtilis and B. megaterium are consistent with measurements in the liter

33 roaches, here we identify GvpU from Priestia megaterium as a protein that regulates GV clustering in

34 the crystal structure of P(46) from Bacillus megaterium at 3.0 A resolution and the fact that P(46) m

35 lus cereus, Bacillus licheniformis, Bacillus megaterium, Bacillus subtilis (including Bacillus niger

36 Among 12 microorganisms tested, Bacillus megaterium, Bacillus subtilis, Staphyloccocus aureus and

37 structed consisting of the E. coli or the B. megaterium beta subunit carrying the C-terminal 18% of t

38 yed the energy-coupling defect, while the B. megaterium beta subunit carrying the E. coli C-terminal

39 vidence of nutrient extraction from Bacillus megaterium by Bacillus subtilis.

40 illus subtilis can kill and prey on Bacillus megaterium by delivering a toxin and extracting nutrient

41 The E. coli beta subunit carrying the B. megaterium C-terminal region displayed the energy-coupli

42 The Bacillus megaterium cbiF, encoding the cobalt-precorrin-4 S-adeno

43 P450 monooxygenase (P450(BM3) from Bacillus megaterium, CYP102A1) has promiscuous activity for oxida

44 charide substrates using engineered Bacillus megaterium cytochrome P450 (P450(BM3)) demethylases that

45 heme and FMN-containing domains of Bacillus megaterium cytochrome P450BM-3 indicates that the proxim

46 derived from a cytochrome P450 from Bacillus megaterium deliver an alpha-cyanocarbene into the alpha-

47 yme was homologously produced in the host B. megaterium DSM319.

48 teria such as Bacillus subtilis and Bacillus megaterium for development of luminescent sensing system

49 We also show that TubR from Bacillus megaterium forms a helical superstructure resembling tha

50 has been linked to a plasmid-borne Bacillus megaterium gene cluster that contains four genes: oxsA,

51 omain (NTD) of the A subunit of the Bacillus megaterium GerK(3) GR, revealing two distinct globular s

52 s, the presence of anhydromuropeptides in B. megaterium germination exudates, which is indicative of

53 ntial amino acids by mutagenesis of Bacillus megaterium gpr.

54 Bacillus subtilis rapidly inhibits Bacillus megaterium growth by delivering the tRNase toxin WapA.

55 The Gram-positive aerobic bacterium Bacillus megaterium has a complete anaerobic pathway that contain

56 Wild-type CYP102 (P450(BM-3)) from Bacillus megaterium has low activity for the oxidation of the PAH

57 2A1), a fatty acid hydroxylase from Bacillus megaterium, has been extensively studied over a period o

58 biochemical characterization of the Bacillus megaterium HD domain phosphohydrolase OxsA, involved in

59 gs early in spore germination, as did the B. megaterium homolog of the major B. subtilis chromosomal

60 G host is a Lysinibacillus, and not Bacillus megaterium: identity of host proteins in our mass spectr

61 In vivo, B. megaterium inactivates AHLs by a CYP102A1 dependent mech

62 The germination protease (GPR) of Bacillus megaterium initiates the degradation of small, acid-solu

63 B. megaterium is a commercially available, nonpathogenic ho

64 P450BM-3 from Bacillus megaterium is a widely studied P450 cytochrome in which

65 B. megaterium is able to synthesize vitamin B(12) through a

66 Bacillus megaterium is deep-rooted in the Bacillus phylogeny, mak

67 widely studied cytochrome P450 from Bacillus megaterium, is capable of very efficient oxidation of AH

68 duction of the gerU/gerVB gene cluster to B. megaterium KM extends the range of germinants recognized

69 s revealed that the tyrosinase from Bacillus megaterium (megaTYR) is an enzyme that possesses a broad

70 the six isolates were identified as Bacillus megaterium, one was identified as Bacillus cereus, and o

71 Purification of either recombinant Bacillus megaterium or Synechocystis CbiXL in Escherichia coli, w

72 The Bacillus megaterium P450 BM3 enzyme is a key model system, with s

73 The flavocytochrome P450 BM3 from Priestia megaterium (P450(BM3)) is a self-sufficient monooxygenas

74 of the cytochrome P450 enzyme from Bacillus megaterium (P450-BM3), a highly active His-ligated varia

75 es and a highly conserved lysine onto the B. megaterium P46 crystal structure revealed a striking sim

76 ing of a scCO(2)-tolerant strain of Bacillus megaterium, previously isolated from formation waters fr

77 Spores of Bacillus megaterium QM B1551 germinate in response to a number of

78 s a germinant molecule by spores of Bacillus megaterium QM B1551 has been examined.

79 proximately 53 kb pBM400 plasmid of Bacillus megaterium QM B1551 has been sequenced and characterized

80 examine the function in vivo of the Bacillus megaterium QM B1551 SleB and SleL proteins.

81 erences in germinant recognition of Bacillus megaterium QM B1551 spores containing the GerVB and/or G

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

83 btilis, Bacillus thuringiensis, and Bacillus megaterium, respectively.

84 vating the pH of developing forespores of B. megaterium resulted in rapid utilization of the forespor

85 entury ago in Bacillus subtilis and Bacillus megaterium revealed that newly synthesized phosphatidyle

86 show that a soil bacterial isolate, Bacillus megaterium Sb5, promotes plant infection by Phytophthora

87 B. megaterium sleB cwlJ double mutant strains complemented

88 of either the N- or C-terminal domain of B. megaterium SleB is sufficient for initiation of cortex h

89 B. megaterium SleL appears to be associated with the epimer

90 in-frame fusion joining the 3' end of the B. megaterium spoIIE coding sequence to the 5' end of gfp,

91 exploited the physical dimensions of the B. megaterium sporangium, in conjunction with wide-field de

92 of the membrane, that influence the Bacillus megaterium spore germination response.

93 on, and these processes were increased in B. megaterium spores with a core pH of approximately 7.8.

94 and > or =20-fold lower in B. cereus and B. megaterium spores.

95 as evidenced in the 3D structure of Bacillus megaterium SQase.

96 omplete genome sequences of two important B. megaterium strains, the plasmidless strain DSM319 and QM

97 ed that the tyrosinase variant from Bacillus megaterium, termed megaTYR, has an increased tolerance f

98 abilize the cytoplasmic membrane of Bacillus megaterium than theromacin and hydramacin-1.

99 Stage I germinated spores of Bacillus megaterium that had slightly increased core water conten

100 In B. megaterium, the gvp region carries a cluster of 15 putat

101 In SASP-A and SASP-C of Bacillus megaterium two conserved glutamate residues, which form

102 Tyrosinase from Bacillus megaterium (TyrBm) was previously used to modulate soy g

103 solanacearum, R. metallidurans, and Bacillus megaterium using chemical tests, a siderophore utilizati

104 soluble fatty acid hydroxylase from Bacillus megaterium utilizing tightly bound FAD and FMN cofactors

105 tative gas vesicle genes (gvp) from Bacillus megaterium VT1660 and their functional expression in Esc

106 Cytochrome P450 BM-3 from Bacillus megaterium was engineered using a combination of directe

107 Whereas protection by B. megaterium was linked to impaired egg laying, correspond

108 A Gram-positive spore former (Bacillus megaterium) was distinguished by an abundant peak for cr

109 ant spores of Bacillus subtilis and Bacillus megaterium were isolated in 4 to 12% yields following ge

110 of spores of Bacillus subtilis and Bacillus megaterium were ring shaped.

111 es to the corresponding sequence in Bacillus megaterium, which reflects the consensus sequence for no