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1 F for formation of a functional Z-ring in C. glutamicum.
2 uch as Bacillus subtilis and Corynebacterium glutamicum.
3 vity in the non-CoQ producer Corynebacterium glutamicum.
4 Escherichia coli and GlxR of Corynebacterium glutamicum.
5 lipids from M. smegmatis and Corynebacterium glutamicum.
6 ndicate that NrdH-redoxin is essential in C. glutamicum.
7 ) homologue Cg10062 found in Corynebacterium glutamicum.
8  and deleted its orthologue NCgl2093 from C. glutamicum.
9 to the central metabolism of Corynebacterium glutamicum.
10  in AG polymerization by gene deletion in C. glutamicum.
11  lysine-producing strains of Corynebacterium glutamicum.
12  BL21 (3.65 +/- 0.09 kV/cm), Corynebacterium glutamicum (5.20 +/- 0.20 kV/cm), and Mycobacterium smeg
13 eting to the mycomembrane of Corynebacterium glutamicum, a nonpathogenic member of the Corynebacteria
14 ains of beta-susceptible C. ulcerans, and C. glutamicum, a species non-permissive for beta, were each
15 (Mycobacterium smegmatis and Corynebacterium glutamicum), Alphaproteobacteria (Agrobacterium tumefaci
16 revious results from GlxR of Corynebacterium glutamicum, an example of the CRP/FNR transcription fami
17 xanthin and glucosides) from Corynebacterium glutamicum and Agromyces mediolanus.
18 pite the biotechnological significance of C. glutamicum and biomedical significance of mycomembrane-c
19 Z, BTZ043, was examined in detail against C. glutamicum and C. glutamicum::ubiA.
20 m the industrially important Corynebacterium glutamicum and determined its atomic structure by 3D cry
21 ative glycosyltransferase, NCgl2096, from C. glutamicum and found that it encodes for a novel alpha(1
22 ids to test this strategy in Corynebacterium glutamicum and Mycobacterium smegmatis, organisms that s
23                              Corynebacterium glutamicum and Mycobacterium tuberculosis share a simila
24 e Corynebacterineae, such as Corynebacterium glutamicum and Mycobacterium tuberculosis.
25 yme isocitrate lyase of both Corynebacterium glutamicum and Rhodococcus fascians.
26 cond, we adapt SSAPs for dsDNA editing in C. glutamicum and S. aureus, enabling one-step gene knockou
27 micelles, of intact cells of Corynebacterium glutamicum and show that this method extracts the free O
28 ransport to the periplasm in Corynebacterium glutamicum and that acetylation is mediated by the membr
29 cation (RM) system CglI from Corynebacterium glutamicum and the homologous NgoAVII RM system from Nei
30  during its production using Corynebacterium glutamicum and uncover the membrane rigidifying effect o
31 vestigated the ability of LM and LAM from C. glutamicum, and C. glutamicumDeltamptC and C. glutamicum
32 ssue, goosefish islet cells, Corynebacterium glutamicum, and Escherichia coli supplied with either [2
33  bacteria Bacillus subtilis, Corynebacterium glutamicum, and Helicobacter pylori.
34 and accumulation studies using E. coli or C. glutamicum arsenite permease mutants clearly show that C
35  sequences has enabled the utilization of C. glutamicum as a model for the identification and study o
36 pic profiling analysis using Corynebacterium glutamicum as a model.
37              Herein, we used Corynebacterium glutamicum as a source of lipoglycan intermediates for h
38 ycobacterium tuberculosis or Corynebacterium glutamicum as microbial antigens that stimulated various
39 GRAS" (General recognized as safe) strain C. glutamicum ATCC 13032 (CgNal).
40 biosynthesis flux network of Corynebacterium glutamicum (ATCC 21799) under glucose limitation in cont
41 c activity of Corynebacterium glutamicum (C. glutamicum ATCC13032) as typical microorganism in fermen
42  acids in the model organism Corynebacterium glutamicum by a mechanism that relies on the mycoloyltra
43 or the metabolic activity of Corynebacterium glutamicum (C. glutamicum ATCC13032) as typical microorg
44 ively provide a topography of the unusual C. glutamicum cell surface, features of which are shared by
45 sphatidylglycerol content, i.e. in intact C. glutamicum cells or in proteoliposomes mimicking the com
46 f oxidized NrdH-redoxin from Corynebacterium glutamicum (Cg) at 1.5 A resolution.
47  of three Acr3 proteins from Corynebacterium glutamicum, CgAcr3-1, CgAcr3-2, and CgAcr3-3.
48 ges Cog and CL31 that infect Corynebacterium glutamicum (Cglu), a model member of the Corynebacterial
49 cient to enhance the bacterial fitness of C. glutamicum cultured in the presence of certain antimicro
50      Deletion of NCgl2100 and NCgl2097 in C. glutamicum demonstrated their role in the biosynthesis o
51 eae 170 and a homologue from Corynebacterium glutamicum designated Cg10062 are 34% identical in seque
52 ee-dimensional structures of Corynebacterium glutamicum diaminopimelate dehydrogenase as a binary com
53 sis and three other genes, a Corynebacterium glutamicum dihydrodipicolinate synthetase gene (DHPS), a
54 odel system, we analyzed few Corynebacterium glutamicum DM 1919 pSenLys cells that synthesized l-lysi
55  an identical phenotype comparable to the C. glutamicum emb deletion mutant.
56 ulosis embA and embB mutants, deletion of C. glutamicum emb leads to a highly truncated AG possessing
57                          The Corynebacterium glutamicum enzyme has been cloned, expressed in Escheric
58         Using this approach, we find that C. glutamicum exhibits asymptotically linear single-cell gr
59 ucose facilitator protein in Corynebacterium glutamicum for mannitol production from fructose and for
60                           Deletion of the C. glutamicum gene NCgl2764 (Rv0224c in M. tuberculosis) ab
61 A genome-scale sRNA library covering 2959 C. glutamicum genes is constructed for high-throughput colo
62 t small molecule inhibitors of UGM impede C. glutamicum growth, suggesting that the galactan is criti
63                      Our data reveal that C. glutamicum has a variable cell envelope, with the S-laye
64 he complete genome sequence, Corynebacterium glutamicum has proven useful in the study of orthologous
65 d structural analysis of the Corynebacterium glutamicum homologue of RipA, Cg1735.
66 e recognition of these same mismatches in C. glutamicum in vitro, as well as mutation accumulation st
67 Mycobacterium smegmatis, and Corynebacterium glutamicum, in their native state.
68  Mycobacterium smegmatis and Corynebacterium glutamicum increases mycolate content and decreases glyc
69                              Corynebacterium glutamicum is a diderm bacterium extensively used in the
70                              Corynebacterium glutamicum is an important industrial bacterium as well
71   Our structure shows that the S-layer of C. glutamicum is composed of a hexagonal array of the PS2 p
72         Ala-DAG formation in Corynebacterium glutamicum is dependent on the activity of an aaPGS homo
73                   The transporter BetP in C. glutamicum is essential in maintaining bacterial cell vi
74 lycosyltransferase MshA from Corynebacterium glutamicum (K(i) approximately 1.6 muM).
75          Inactivation of the Corynebacterium glutamicum lpqW ortholog, NCgl1054, resulted in a slow g
76 ic role of LtsA protein from Corynebacterium glutamicum (LtsACg) in the modification by amidation of
77 er coated by a surface (S-)layer array in C. glutamicum, making this cell envelope highly distinctive
78 iposomes mimicking the composition of the C. glutamicum membrane.
79                   Cell-free incubation of C. glutamicum membranes with GDP-[(14)C]Man established tha
80 em, including the following: Corynebacterium glutamicum, Microcuccus luteus, Staphylococcus epidermid
81 similar to that of the t-LM produced by a C. glutamicum mutant lacking the mptA gene, encoding a memb
82 se with membranes prepared from different C. glutamicum mutant strains, we have shown that both NCgl2
83                                   Using a C. glutamicum mutant that lacks arabinan, we identified syn
84           We discovered that Corynebacterium glutamicum mutants lacking components of the pupylation
85 mbranes vesicles from Escherichia coli or C. glutamicum mutants were assayed for efflux with differen
86                        Using Corynebacterium glutamicum mycolyltransferase deletion strains, we impli
87                   Herein, we have studied C. glutamicum NCgl1505, the orthologue of putative glycosyl
88 rized a homologous enzyme of Corynebacterium glutamicum (NCgl2339) and observed that it demycothiolat
89              Deletion of the Corynebacterium glutamicum NCgl2760 gene resulted in a complete loss of
90           PTM site sequence analysis from C. glutamicum OMP and other O-acylated proteins in bacteria
91 Mg(2+) binding severely inhibit growth of C. glutamicum on citrate.
92             For example, the Corynebacterium glutamicum panD(+) gene corrected the pantothenate auxot
93 ction endonuclease CglI from Corynebacterium glutamicum recognizes an asymmetric 5'-GCCGC-3' site and
94 ructures of SAH enzymes from Corynebacterium glutamicum (RelH(Cg)) and Leptospira levettii (RelH(Ll))
95 (NCgl2203) was overexpressed in wild type C. glutamicum, resistance to BTZ043 was further increased.
96                        Deletion of emb in C. glutamicum results in a slow growing mutant with profoun
97 ) Phosphatidylglycerol in the membrane of C. glutamicum seems to stabilize the inactive conformation
98 he physiological function of Corynebacterium glutamicum SepF, the only cell division-associated prote
99 cobacterium tuberculosis and Corynebacterium glutamicum share a similar cell wall structure and ortho
100  Mycobacterium smegmatis and Corynebacterium glutamicum, showing that OdhA is an 800-kDa homohexamer
101 Glc in shake flasks, whereas an engineered C glutamicum strain could efficiently convert the precurso
102 plications, high performance Corynebacterium glutamicum strains capable of producing valerolactam (bu
103 anes with GDP-[(14)C]Man established that C. glutamicum synthesized a novel alpha(1-->6)-linked linea
104 ed the tetRO region from the Corynebacterium glutamicum TetZ locus into a mycobacterial shuttle plasm
105 two open reading frames from Corynebacterium glutamicum that encode for putative GT-Cs.
106 e-dependent mannosyltransferase MgtA from C. glutamicum that extends GlcAGroAc2.
107 structed in S cerevisiae and Corynebacterium glutamicum The best-performing S cerevisiae strain was c
108       Additionally, disruption of ubiA in C. glutamicum, the first enzyme involved in the biosynthesi
109 Like the homologue OdhI from Corynebacterium glutamicum, the unphosphorylated form of GarA is shown t
110  strain was sensitive to BTZ043; however, C. glutamicum::ubiA was found to be resistant, despite poss
111 mined in detail against C. glutamicum and C. glutamicum::ubiA.
112 e apically growing bacterium Corynebacterium glutamicum using a novel broadly applicable inference me
113 his, we investigated the cell envelope of C. glutamicum using electron cryotomography and cryomicrosc
114   The structure of MshA from Corynebacterium glutamicum was determined both in the absence of substra
115 ne betaine carrier BetP from Corynebacterium glutamicum was recently shown to function as both an osm
116 ms by which OMP precursors were sorted in C. glutamicum, we first investigated the partitioning of en
117  tools in the model organism Corynebacterium glutamicum, we identified approximately 30 candidate O-m
118 liphilus metalliredigens and Corynebacterium glutamicum were cloned and expressed in Escherichia coli
119  structure of the TR LysG of Corynebacterium glutamicum, which detects all three basic amino acids.
120 eae encompasses species like Corynebacterium glutamicum, which has been harnessed for industrial prod
121 uclease from Actinobacterium Corynebacterium glutamicum, which recognizes mismatched substrates in vi
122                    Treatment of wild-type C. glutamicum with ethambutol and subsequent cell wall anal
123 tuberculosis and NCgl1822 in Corynebacterium glutamicum, with 10 predicted transmembrane domains and
124                    When the gene encoding C. glutamicum Z-decaprenyl-diphosphate synthase (NCgl2203)

 
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