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1                                              M. luteus is capable of long-chain alkene biosynthesis,
2                                 The use of a M. luteus translation system provides a method for incor
3    In contrast to most other actinobacteria, M. luteus encodes only one resuscitation-promoting facto
4 proteins show cross-species activity against M. luteus, Mycobacterium smegmatis and M. bovis (BCG).
5 ocyanin (PLA) pigmentation in M. cupreus and M. luteus var. variegatus occurred via separate yet stri
6 us), and progenitor species (M. guttatus and M. luteus).
7       Uniquely among characterized bacteria, M. luteus appears to be able to metabolize glycogen only
8         Induction of the Cecropin A1 gene by M. luteus required Relish, whereas induction of the Cecr
9 aled by its activity in zymograms containing M. luteus cell walls and its ability to (i) cause lysis
10  function of its Rho factor is essential for M. luteus and that growth of a gram-positive organism ca
11                            PG extracted from M. luteus induced Cecropin A in Relish mutants, whereas
12 sole source of carbon for energy and growth, M. luteus has a minimal complement of genes concerned wi
13 gene of one of only two rrn operons found in M. luteus.
14 e hypothesis that the sequence is present in M. luteus Rho to facilitate its binding to M. luteus tra
15  which restores active growth to cultures of M. luteus rendered dormant by prolonged incubation in st
16                   The glucosyltransferase of M. luteus, which participates in the biosynthesis of tei
17              Rpf was essential for growth of M. luteus.
18                      The high sensitivity of M. luteus to beta-lactam antibiotics may result from the
19 al from fluorescamine-labelled cell walls of M. luteus; and (iii) hydrolyse the artificial lysozyme s
20                            The other parent, M. luteus, was restricted to a single locality.
21 o either diploid (M. guttatus) or polyploid (M. luteus and M. x robertsii) samples.
22 ive (E. coli) bacterium and a Gram-positive (M. luteus) bacterium and the differences were attributed
23                                          The M. luteus Rho polypeptide has 690 residues, which is 271
24                                          The M. luteus Rpf is a secreted approximately 16-kDa protein
25                                 However, the M. luteus protein has a less stringent RNA cofactor spec
26 eferences for subsets of the linkages in the M. luteus peptidoglycan.
27 antibiotic that inhibits the activity of the M. luteus transcription termination factor Rho.
28        Biochemical studies indicate that the M. luteus protein is very similar to E. coli Rho in term
29                                    Thus, the M. luteus protein functions as a true Rho factor, but wi
30 n M. luteus Rho to facilitate its binding to M. luteus transcripts, which are likely to have a high d
31                               In contrast to M. luteus, for which rpf is an essential gene, we find t
32 uence, des(60-300) Rho, to that of wild-type M. luteus Rho.
33 rs in reactions of D52A ChEWL and GoEWL with M. luteus peptidoglycans, with the glycine carboxyl grou
34 tive and negative ions and not observed with M. luteus.

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