ライフサイエンスコーパス: Bacillus megaterium

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

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

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

4 constructed in flavocytochrome P450 BM3 from Bacillus megaterium.

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

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

7 that Bacillus subtilis can kill and prey on 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 In Bacillus megaterium and Bacillus subtilis, energization

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

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

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

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

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

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

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

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

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

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

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

33 ytochrome P450 monooxygenase (P450(BM3) from Bacillus megaterium, CYP102A1) has promiscuous activity

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

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

36 sferases derived from a cytochrome P450 from Bacillus megaterium deliver an alpha-cyanocarbene into t

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

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

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

40 erminal domain (NTD) of the A subunit of the Bacillus megaterium GerK(3) GR, revealing two distinct g

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

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

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

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

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

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

47 he phage G host is a Lysinibacillus, and not Bacillus megaterium: identity of host proteins in our ma

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

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

50 Bacillus megaterium is deep-rooted in the Bacillus phylo

51 102A1, a widely studied cytochrome P450 from Bacillus megaterium, is capable of very efficient oxidat

52 candidates revealed that the tyrosinase from Bacillus megaterium (megaTYR) is an enzyme that possesse

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

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

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

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

57 engineering of a scCO(2)-tolerant strain of Bacillus megaterium, previously isolated from formation

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

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

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

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

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

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

64 cillus subtilis, Bacillus thuringiensis, and Bacillus megaterium, respectively.

65 half a century ago in Bacillus subtilis and Bacillus megaterium revealed that newly synthesized phos

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

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

68 ve site, as evidenced in the 3D structure of Bacillus megaterium SQase.

69 we observed that the tyrosinase variant from Bacillus megaterium, termed megaTYR, has an increased to

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

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

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

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

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

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

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

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

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

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

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

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