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

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

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

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

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

11 Corynebacterium glutamicum and Mycobacterium tuberculosi

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

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

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

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

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

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

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

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

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

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

22 The three-dimensional structures of Corynebacterium glutamicum diaminopimelate dehydrogenase

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

24 The Corynebacterium glutamicum enzyme has been cloned, expre

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

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

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

28 802 orthologs in Mycobacterium smegmatis and Corynebacterium glutamicum increases mycolate content an

29 Corynebacterium glutamicum is an important industrial ba

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

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

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

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

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

35 We discovered that Corynebacterium glutamicum mutants lacking components of

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

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

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

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

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

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

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

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

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

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

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

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

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