ライフサイエンスコーパス: glycopeptidolipid

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1 artially purified lipid fractions containing glycopeptidolipids.

2 the surface correlates with the presence of glycopeptidolipids, a mycobacterium-specific class of am

3 phenotype that expresses minimal amounts of glycopeptidolipid and is unable to form biofilms.

4 All mutants lacked glycopeptidolipids and were unable to form biofilms on p

5 ming, smooth colony phenotype that expresses glycopeptidolipid, and an invasive rough colony phenotyp

6 se-6-deoxytalose-) of the serovar 2-specific glycopeptidolipid, and revealed a locus (ser2A) encoding

7 resence of highly antigenic, surface-exposed glycopeptidolipids, and these glycolipids possess varian

8 nlike, previously described serovar-specific glycopeptidolipid antigens.

9 structurally similar to previously described glycopeptidolipid antigens.

10 on of rtfA will permit further evaluation of glycopeptidolipid biosynthesis and the construction of i

11 One of these clusters encodes glycopeptidolipid biosynthesis enzymes which have not pr

12 avium clones identified one gene involved in glycopeptidolipid biosynthesis, one gene encoding the co

13 rtions in the mps gene, which is involved in glycopeptidolipid biosynthesis.

14 rature-dependent loss or physical removal of glycopeptidolipid from the cell wall of one of the smoot

15 M. abscessus exists as either a glycopeptidolipid (GPL) expressing variant (smooth pheno

16 The preparation of the glycopeptidolipid (GPL) present in the cell wall of Myco

17 Transitioning from a smooth (S) high-glycopeptidolipid (GPL) producer to a rough (R) low-GPL

18 ss of an antigenic surface structure, termed glycopeptidolipid (GPL), by rough variants.

19 ium abscessus has been implicated in loss of glycopeptidolipid (GPL), increased pathogenicity, and cl

20 these strains possesses characteristic polar glycopeptidolipids (GPL) which are sufficiently differen

21 The absence of glycopeptidolipids (GPLs) abolishes the ability of mycob

22 Glycopeptidolipids (GPLs) are dominant cell surface mole

23 M. avium express glycopeptidolipids (GPLs) as a major cell wall constitue

24 nt studies from our laboratory indicate that glycopeptidolipids (GPLs), a major surface component of

25 agosomes containing silica beads coated with glycopeptidolipids (GPLs), a major surface component of

26 us rough (R) variant, devoid of cell-surface glycopeptidolipids (GPLs), causes more severe clinical d

27 nsferase D is involved in the methylation of glycopeptidolipids (GPLs); highly antigenic glycolipids

28 This suggests that glycopeptidolipid in the outermost portion of the M. abs

29 r, such mutants will help define the role of glycopeptidolipids in the intracellular survival of thes

30 distinct from the type- and species-specific glycopeptidolipids, lipooligosaccharides, phenolic glyco

31 ne strain (S-type) contained no identifiable glycopeptidolipids or lipopentapeptide (L5P), yet both l

32 ated by biofilm formation, with M. abscessus glycopeptidolipids playing an important role.

33 surface lipids, no difference is observed in glycopeptidolipids, polar lipids, apolar lipids, or myco

34 Further, a suppressor mutation in a glycopeptidolipid synthesis gene (mps) that results in h

35 ium smegmatis, and the resulting recombinant glycopeptidolipids were characterized by thin-layer chro

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