ライフサイエンスコーパス: glutamicum

1 Escherichia coli and GlxR of Corynebacterium glutamicum.

2 lipids from M. smegmatis and Corynebacterium glutamicum.

3 ndicate that NrdH-redoxin is essential in C. glutamicum.

4 ) homologue Cg10062 found in Corynebacterium glutamicum.

5 and deleted its orthologue NCgl2093 from C. glutamicum.

6 to the central metabolism of Corynebacterium glutamicum.

7 in AG polymerization by gene deletion in C. glutamicum.

8 lysine-producing strains of Corynebacterium glutamicum.

9 BL21 (3.65 +/- 0.09 kV/cm), Corynebacterium glutamicum (5.20 +/- 0.20 kV/cm), and Mycobacterium smeg

10 eting to the mycomembrane of Corynebacterium glutamicum, a nonpathogenic member of the Corynebacteria

11 ains of beta-susceptible C. ulcerans, and C. glutamicum, a species non-permissive for beta, were each

12 revious results from GlxR of Corynebacterium glutamicum, an example of the CRP/FNR transcription fami

13 xanthin and glucosides) from Corynebacterium glutamicum and Agromyces mediolanus.

14 Z, BTZ043, was examined in detail against C. glutamicum and C. glutamicum::ubiA.

15 ative glycosyltransferase, NCgl2096, from C. glutamicum and found that it encodes for a novel alpha(1

16 Corynebacterium glutamicum and Mycobacterium tuberculosis share a simila

17 e Corynebacterineae, such as Corynebacterium glutamicum and Mycobacterium tuberculosis.

18 yme isocitrate lyase of both Corynebacterium glutamicum and Rhodococcus fascians.

19 micelles, of intact cells of Corynebacterium glutamicum and show that this method extracts the free O

20 cation (RM) system CglI from Corynebacterium glutamicum and the homologous NgoAVII RM system from Nei

21 vestigated the ability of LM and LAM from C. glutamicum, and C. glutamicumDeltamptC and C. glutamicum

22 ssue, goosefish islet cells, Corynebacterium glutamicum, and Escherichia coli supplied with either [2

23 and accumulation studies using E. coli or C. glutamicum arsenite permease mutants clearly show that C

24 sequences has enabled the utilization of C. glutamicum as a model for the identification and study o

25 Herein, we used Corynebacterium glutamicum as a source of lipoglycan intermediates for h

26 ycobacterium tuberculosis or Corynebacterium glutamicum as microbial antigens that stimulated various

27 GRAS" (General recognized as safe) strain C. glutamicum ATCC 13032 (CgNal).

28 biosynthesis flux network of Corynebacterium glutamicum (ATCC 21799) under glucose limitation in cont

29 sphatidylglycerol content, i.e. in intact C. glutamicum cells or in proteoliposomes mimicking the com

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

31 of three Acr3 proteins from Corynebacterium glutamicum, CgAcr3-1, CgAcr3-2, and CgAcr3-3.

32 cient to enhance the bacterial fitness of C. glutamicum cultured in the presence of certain antimicro

33 Deletion of NCgl2100 and NCgl2097 in C. glutamicum demonstrated their role in the biosynthesis o

34 eae 170 and a homologue from Corynebacterium glutamicum designated Cg10062 are 34% identical in seque

35 ee-dimensional structures of Corynebacterium glutamicum diaminopimelate dehydrogenase as a binary com

36 sis and three other genes, a Corynebacterium glutamicum dihydrodipicolinate synthetase gene (DHPS), a

37 an identical phenotype comparable to the C. glutamicum emb deletion mutant.

38 ulosis embA and embB mutants, deletion of C. glutamicum emb leads to a highly truncated AG possessing

39 The Corynebacterium glutamicum enzyme has been cloned, expressed in Escheric

40 ucose facilitator protein in Corynebacterium glutamicum for mannitol production from fructose and for

41 t small molecule inhibitors of UGM impede C. glutamicum growth, suggesting that the galactan is criti

42 he complete genome sequence, Corynebacterium glutamicum has proven useful in the study of orthologous

43 Mycobacterium smegmatis, and Corynebacterium glutamicum, in their native state.

44 Mycobacterium smegmatis and Corynebacterium glutamicum increases mycolate content and decreases glyc

45 Corynebacterium glutamicum is an important industrial bacterium as well

46 Ala-DAG formation in Corynebacterium glutamicum is dependent on the activity of an aaPGS homo

47 lycosyltransferase MshA from Corynebacterium glutamicum (K(i) approximately 1.6 muM).

48 Inactivation of the Corynebacterium glutamicum lpqW ortholog, NCgl1054, resulted in a slow g

49 ic role of LtsA protein from Corynebacterium glutamicum (LtsACg) in the modification by amidation of

50 iposomes mimicking the composition of the C. glutamicum membrane.

51 Cell-free incubation of C. glutamicum membranes with GDP-[(14)C]Man established tha

52 em, including the following: Corynebacterium glutamicum, Microcuccus luteus, Staphylococcus epidermid

53 similar to that of the t-LM produced by a C. glutamicum mutant lacking the mptA gene, encoding a memb

54 se with membranes prepared from different C. glutamicum mutant strains, we have shown that both NCgl2

55 We discovered that Corynebacterium glutamicum mutants lacking components of the pupylation

56 mbranes vesicles from Escherichia coli or C. glutamicum mutants were assayed for efflux with differen

57 Herein, we have studied C. glutamicum NCgl1505, the orthologue of putative glycosyl

58 rized a homologous enzyme of Corynebacterium glutamicum (NCgl2339) and observed that it demycothiolat

59 Deletion of the Corynebacterium glutamicum NCgl2760 gene resulted in a complete loss of

60 PTM site sequence analysis from C. glutamicum OMP and other O-acylated proteins in bacteria

61 Mg(2+) binding severely inhibit growth of C. glutamicum on citrate.

62 For example, the Corynebacterium glutamicum panD(+) gene corrected the pantothenate auxot

63 ction endonuclease CglI from Corynebacterium glutamicum recognizes an asymmetric 5'-GCCGC-3' site and

64 (NCgl2203) was overexpressed in wild type C. glutamicum, resistance to BTZ043 was further increased.

65 Deletion of emb in C. glutamicum results in a slow growing mutant with profoun

66 ) Phosphatidylglycerol in the membrane of C. glutamicum seems to stabilize the inactive conformation

67 cobacterium tuberculosis and Corynebacterium glutamicum share a similar cell wall structure and ortho

68 anes with GDP-[(14)C]Man established that C. glutamicum synthesized a novel alpha(1-->6)-linked linea

69 ed the tetRO region from the Corynebacterium glutamicum TetZ locus into a mycobacterial shuttle plasm

70 two open reading frames from Corynebacterium glutamicum that encode for putative GT-Cs.

71 e-dependent mannosyltransferase MgtA from C. glutamicum that extends GlcAGroAc2.

72 Additionally, disruption of ubiA in C. glutamicum, the first enzyme involved in the biosynthesi

73 Like the homologue OdhI from Corynebacterium glutamicum, the unphosphorylated form of GarA is shown t

74 strain was sensitive to BTZ043; however, C. glutamicum::ubiA was found to be resistant, despite poss

75 mined in detail against C. glutamicum and C. glutamicum::ubiA.

76 The structure of MshA from Corynebacterium glutamicum was determined both in the absence of substra

77 ne betaine carrier BetP from Corynebacterium glutamicum was recently shown to function as both an osm

78 ms by which OMP precursors were sorted in C. glutamicum, we first investigated the partitioning of en

79 liphilus metalliredigens and Corynebacterium glutamicum were cloned and expressed in Escherichia coli

80 eae encompasses species like Corynebacterium glutamicum, which has been harnessed for industrial prod

81 Treatment of wild-type C. glutamicum with ethambutol and subsequent cell wall anal

82 tuberculosis and NCgl1822 in Corynebacterium glutamicum, with 10 predicted transmembrane domains and

83 When the gene encoding C. glutamicum Z-decaprenyl-diphosphate synthase (NCgl2203)