ライフサイエンスコーパス: M. luteus

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 ikingly, the proportion of flies dying after M. luteus infection was significantly lower when flies w

5 proteins show cross-species activity against M. luteus, Mycobacterium smegmatis and M. bovis (BCG).

6 ocyanin (PLA) pigmentation in M. cupreus and M. luteus var. variegatus occurred via separate yet stri

7 us), and progenitor species (M. guttatus and M. luteus).

8 hibit the growth of E. coli, C. xerosis, and M. luteus with a 99% efficiency.

9 Uniquely among characterized bacteria, M. luteus appears to be able to metabolize glycogen only

10 Induction of the Cecropin A1 gene by M. luteus required Relish, whereas induction of the Cecr

11 aled by its activity in zymograms containing M. luteus cell walls and its ability to (i) cause lysis

12 ted with five test bacteria: S. epidermidis, M. luteus, E. hirae, B. subtilis, and E. coli.

13 function of its Rho factor is essential for M. luteus and that growth of a gram-positive organism ca

14 PG extracted from M. luteus induced Cecropin A in Relish mutants, whereas

15 were associated with enhanced survival from M. luteus + E. faecalis infection.

16 sole source of carbon for energy and growth, M. luteus has a minimal complement of genes concerned wi

17 gene of one of only two rrn operons found in M. luteus.

18 e hypothesis that the sequence is present in M. luteus Rho to facilitate its binding to M. luteus tra

19 The two inherited M. luteus subgenomes, genetically distinct but epigeneti

20 P. aeruginosa (15 mm), B. subtilis (15 mm), M. luteus (14 mm) and C. albicans (15 mm), with a MIC of

21 which restores active growth to cultures of M. luteus rendered dormant by prolonged incubation in st

22 The glucosyltransferase of M. luteus, which participates in the biosynthesis of tei

23 Rpf was essential for growth of M. luteus.

24 The high sensitivity of M. luteus to beta-lactam antibiotics may result from the

25 al from fluorescamine-labelled cell walls of M. luteus; and (iii) hydrolyse the artificial lysozyme s

26 osperm and seed abortion when M. guttatus or M. luteus is seed parent, respectively, and transgressiv

27 The other parent, M. luteus, was restricted to a single locality.

28 o either diploid (M. guttatus) or polyploid (M. luteus and M. x robertsii) samples.

29 ive (E. coli) bacterium and a Gram-positive (M. luteus) bacterium and the differences were attributed

30 The M. luteus Rho polypeptide has 690 residues, which is 271

31 The M. luteus Rpf is a secreted approximately 16-kDa protein

32 However, the M. luteus protein has a less stringent RNA cofactor spec

33 eferences for subsets of the linkages in the M. luteus peptidoglycan.

34 antibiotic that inhibits the activity of the M. luteus transcription termination factor Rho.

35 Biochemical studies indicate that the M. luteus protein is very similar to E. coli Rho in term

36 Thus, the M. luteus protein functions as a true Rho factor, but wi

37 n M. luteus Rho to facilitate its binding to M. luteus transcripts, which are likely to have a high d

38 In contrast to M. luteus, for which rpf is an essential gene, we find t

39 uence, des(60-300) Rho, to that of wild-type M. luteus Rho.

40 rs in reactions of D52A ChEWL and GoEWL with M. luteus peptidoglycans, with the glycine carboxyl grou

41 tive and negative ions and not observed with M. luteus.