ライフサイエンスコーパス: Corynebacterium glutamicum

1 factors, CAP of Escherichia coli and GlxR of Corynebacterium glutamicum.

2 GlcAGroAc2 glycolipids from M. smegmatis and Corynebacterium glutamicum.

3 enase ( cis-CaaD) homologue Cg10062 found in Corynebacterium glutamicum.

4 the application to the central metabolism of Corynebacterium glutamicum.

5 e improvement of lysine-producing strains of Corynebacterium glutamicum.

6 tive bacteria, such as Bacillus subtilis and Corynebacterium glutamicum.

7 rboxylation activity in the non-CoQ producer Corynebacterium glutamicum.

8 Escherichia coli BL21 (3.65 +/- 0.09 kV/cm), Corynebacterium glutamicum (5.20 +/- 0.20 kV/cm), and My

9 ble for OMP targeting to the mycomembrane of Corynebacterium glutamicum, a nonpathogenic member of th

10 : Actinomycetia (Mycobacterium smegmatis and Corynebacterium glutamicum), Alphaproteobacteria (Agroba

11 om analysis of previous results from GlxR of Corynebacterium glutamicum, an example of the CRP/FNR tr

12 noids (decaprenoxanthin and glucosides) from Corynebacterium glutamicum and Agromyces mediolanus.

13 PS2 S-layers from the industrially important Corynebacterium glutamicum and determined its atomic str

14 nosyl phospholipids to test this strategy in Corynebacterium glutamicum and Mycobacterium smegmatis,

15 nose (DPA) in the Corynebacterineae, such as Corynebacterium glutamicum and Mycobacterium tuberculosi

16 Corynebacterium glutamicum and Mycobacterium tuberculosi

17 arity to the enzyme isocitrate lyase of both Corynebacterium glutamicum and Rhodococcus fascians.

18 erse surfactant micelles, of intact cells of Corynebacterium glutamicum and show that this method ext

19 its efficient transport to the periplasm in Corynebacterium glutamicum and that acetylation is media

20 striction-modification (RM) system CglI from Corynebacterium glutamicum and the homologous NgoAVII RM

21 ne and cell wall during its production using Corynebacterium glutamicum and uncover the membrane rigi

22 dymal adipose tissue, goosefish islet cells, Corynebacterium glutamicum, and Escherichia coli supplie

23 ionarily distant bacteria Bacillus subtilis, Corynebacterium glutamicum, and Helicobacter pylori.

24 ome-wide phenotypic profiling analysis using Corynebacterium glutamicum as a model.

25 Herein, we used Corynebacterium glutamicum as a source of lipoglycan int

26 linositol from Mycobacterium tuberculosis or Corynebacterium glutamicum as microbial antigens that st

27 t of the lysine biosynthesis flux network of Corynebacterium glutamicum (ATCC 21799) under glucose li

28 ied with mycolic acids in the model organism Corynebacterium glutamicum by a mechanism that relies on

29 veloped to monitor the metabolic activity of Corynebacterium glutamicum (C. glutamicum ATCC13032) as

30 -ray structure of oxidized NrdH-redoxin from Corynebacterium glutamicum (Cg) at 1.5 A resolution.

31 zed the function of three Acr3 proteins from Corynebacterium glutamicum, CgAcr3-1, CgAcr3-2, and CgAc

32 e use of the phages Cog and CL31 that infect Corynebacterium glutamicum (Cglu), a model member of the

33 udomonas pavonaceae 170 and a homologue from Corynebacterium glutamicum designated Cg10062 are 34% id

34 The three-dimensional structures of Corynebacterium glutamicum diaminopimelate dehydrogenase

35 ycerol biosynthesis and three other genes, a Corynebacterium glutamicum dihydrodipicolinate synthetas

36 a biocatalytic model system, we analyzed few Corynebacterium glutamicum DM 1919 pSenLys cells that sy

37 The Corynebacterium glutamicum enzyme has been cloned, expre

38 genase, and a glucose facilitator protein in Corynebacterium glutamicum for mannitol production from

39 vailability of the complete genome sequence, Corynebacterium glutamicum has proven useful in the stud

40 biochemical, and structural analysis of the Corynebacterium glutamicum homologue of RipA, Cg1735.

41 rium bovis BCG, Mycobacterium smegmatis, and Corynebacterium glutamicum, in their native state.

42 802 orthologs in Mycobacterium smegmatis and Corynebacterium glutamicum increases mycolate content an

43 Corynebacterium glutamicum is a diderm bacterium extensi

44 Corynebacterium glutamicum is an important industrial ba

45 Ala-DAG formation in Corynebacterium glutamicum is dependent on the activity

46 the retaining glycosyltransferase MshA from Corynebacterium glutamicum (K(i) approximately 1.6 muM).

47 Inactivation of the Corynebacterium glutamicum lpqW ortholog, NCgl1054, resu

48 ating the specific role of LtsA protein from Corynebacterium glutamicum (LtsACg) in the modification

49 sed DOX-PCA system, including the following: Corynebacterium glutamicum, Microcuccus luteus, Staphylo

50 We discovered that Corynebacterium glutamicum mutants lacking components of

51 Using Corynebacterium glutamicum mycolyltransferase deletion s

52 we also characterized a homologous enzyme of Corynebacterium glutamicum (NCgl2339) and observed that

53 Deletion of the Corynebacterium glutamicum NCgl2760 gene resulted in a c

54 For example, the Corynebacterium glutamicum panD(+) gene corrected the pa

55 The restriction endonuclease CglI from Corynebacterium glutamicum recognizes an asymmetric 5'-G

56 esent crystal structures of SAH enzymes from Corynebacterium glutamicum (RelH(Cg)) and Leptospira lev

57 we investigate the physiological function of Corynebacterium glutamicum SepF, the only cell division-

58 Mycobacterium tuberculosis and Corynebacterium glutamicum share a similar cell wall str

59 ive enzymes from Mycobacterium smegmatis and Corynebacterium glutamicum, showing that OdhA is an 800-

60 c engineering applications, high performance Corynebacterium glutamicum strains capable of producing

61 We have sub-cloned the tetRO region from the Corynebacterium glutamicum TetZ locus into a mycobacteri

62 d characterized two open reading frames from Corynebacterium glutamicum that encode for putative GT-C

63 roside was reconstructed in S cerevisiae and Corynebacterium glutamicum The best-performing S cerevis

64 Like the homologue OdhI from Corynebacterium glutamicum, the unphosphorylated form of

65 h behavior of the apically growing bacterium Corynebacterium glutamicum using a novel broadly applica

66 The structure of MshA from Corynebacterium glutamicum was determined both in the ab

67 The glycine betaine carrier BetP from Corynebacterium glutamicum was recently shown to functio

68 Using these tools in the model organism Corynebacterium glutamicum, we identified approximately

69 logues from Alkaliphilus metalliredigens and Corynebacterium glutamicum were cloned and expressed in

70 re, we solve the structure of the TR LysG of Corynebacterium glutamicum, which detects all three basi

71 r Corynebacterineae encompasses species like Corynebacterium glutamicum, which has been harnessed for

72 ndoMS/NucS endonuclease from Actinobacterium Corynebacterium glutamicum, which recognizes mismatched

73 n Mycobacterium tuberculosis and NCgl1822 in Corynebacterium glutamicum, with 10 predicted transmembr