ライフサイエンスコーパス: M. capricolum

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1 titution experiments with proteins from both M. capricolum and E. coli showed that EI(DeltaHD) can do

2 Ser) kinase, was demonstrated in extracts of M. capricolum and Mycoplasma genitalium.

3 nsfer to HPrs from E. coli, B. subtilis, and M. capricolum as well as to EIAglc from E. coli.

4 es are located diametrically opposite in the M. capricolum chromosome.

5 Gram-negative glycerol kinase activity, the M. capricolum EIIA has no effect on the homologous glyce

6 M. capricolum EIIA was unreactive with antibodies direct

7 Enzyme I (64,600 Mr) from M. capricolum exhibited a monomer-dimer-tetramer associa

8 Molecular modeling comparisons of M. capricolum HPr and the chimeric construct provided a

9 , and 51-53 are important for recognition of M. capricolum HPr by its cognate HPr(Ser) kinase.

10 e information and its transplantation into a M. capricolum recipient cell to create new M. mycoides c

11 Furthermore, M. capricolum recombinant C-terminal domain of enzyme I

12 I to enzyme IIAglc (EIIAglc) from E. coli or M. capricolum requires the intermediacy of HPr.

13 Subsequent analysis of the M. capricolum RNAs by mass spectrometry shows that the T

14 o specific peptide determinants of predicted M. capricolum subsp. capricolum gene products, and (iii)

15 These occur at two separate loci in the M. capricolum subsp. capricolum genome, which shares str

16 the mycoides cluster, including a strain of M. capricolum subsp. capricolum identical to that found

17 A to vmcF) expressing distinct Vmc (variable M. capricolum subsp. capricolum) lipoproteins is demonst

18 lysis of the membrane-associated proteome of M. capricolum subsp. capricolum, a novel set of six gene

19 n a latex agglutination test (LAT), detected M. capricolum subsp. capripneumoniae antigen in the seru

20 tinated strongly in the presence of purified M. capricolum subsp. capripneumoniae capsular polysaccha

21 icity of the LAT exactly mirrored that of an M. capricolum subsp. capripneumoniae CPS-specific monocl

22 The LAT detected all 11 strains of M. capricolum subsp. capripneumoniae examined in this st

23 using genomic DNA and bacterial culture from M. capricolum subsp. capripneumoniae strain ILRI181, whi

24 he assay using a specific target sequence in M. capricolum subsp. capripneumoniae, as found in the ge

25 ed agglutinating activity in the presence of M. capricolum subsp. capripneumoniae, strongly suggestin

26 ase amplification (RPA) for the detection of M. capricolum subsp. capripneumoniae.

27 h approximately 50% alpha-helix content from M. capricolum were used to further elucidate the nature

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