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Volumn 105, Issue 12, 2005, Pages 4610-4660

Syntheses around the transglycosylation step in peptidoglycan biosynthesis

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTICS; BACTERIA; ENZYMES; LIPIDS; MOLECULAR STRUCTURE; MONOMERS; POLYPEPTIDES; POLYSACCHARIDES;

EID: 30744442513     PISSN: 00092665     EISSN: None     Source Type: Journal    
DOI: 10.1021/cr040634e     Document Type: Review
Times cited : (70)

References (307)
  • 2
    • 0000960760 scopus 로고    scopus 로고
    • Review: Barton, D., Nakanishi, K., Eds.; Elsevier: Amsterdam
    • Review: Bugg, T. D. H. In Comprehensive Natural Products Chemistry; Barton, D., Nakanishi, K., Eds.; Elsevier: Amsterdam, 1999; Vol. 3, p 241.
    • (1999) Comprehensive Natural Products Chemistry , vol.3 , pp. 241
    • Bugg, T.D.H.1
  • 4
    • 30744461889 scopus 로고    scopus 로고
    • note
    • In fact, it is a two-step process with an acylated enzyme intermediate.
  • 9
    • 0027469853 scopus 로고
    • In fact, on SDS-polyacrylamide gels PBP1b consists of at least three bands of varying intensity. However, each of the three components has been shown to possess both transglycosylase and transpeptidase activity. See: and references therein
    • In fact, on SDS-polyacrylamide gels PBP1b consists of at least three bands of varying intensity. However, each of the three components has been shown to possess both transglycosylase and transpeptidase activity. See: Nicholas, R. A.; Lamson, D. R.; Schultz, D. E. J. Biol. Chem. 1993, 5632 and references therein.
    • (1993) J. Biol. Chem. , pp. 5632
    • Nicholas, R.A.1    Lamson, D.R.2    Schultz, D.E.3
  • 18
    • 0033942357 scopus 로고    scopus 로고
    • A recent review on transglycosylase inhibition
    • A recent review on transglycosylase inhibition: Goldman, R. C.; Gange, D. Curr. Med. Chem. 2000, 7, 801.
    • (2000) Curr. Med. Chem. , vol.7 , pp. 801
    • Goldman, R.C.1    Gange, D.2
  • 20
    • 0035965704 scopus 로고    scopus 로고
    • It should be mentioned, however, that in in vitro experiments the time courses of the transglycosylation and the transpeptidation differed. The transpeptidation reaction occurred on a longer time scale than the glycosyl transfer. See
    • It should be mentioned, however, that in in vitro experiments the time courses of the transglycosylation and the transpeptidation differed. The transpeptidation reaction occurred on a longer time scale than the glycosyl transfer. See ref 31.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 11638
    • Schwartz, B.1    Markwalder, J.A.2    Wang, Y.3
  • 29
    • 0037152343 scopus 로고    scopus 로고
    • For work describing syntheses of the disaccharide peptide part, see:
    • For work describing syntheses of the disaccharide peptide part, see: (a) Chowdhury, A. R.; Siriwardeny, A.; Boons, G.-J. Tetrahedron Lett. 2002, 43, 7805.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 7805
    • Chowdhury, A.R.1    Siriwardeny, A.2    Boons, G.-J.3
  • 31
    • 30744471720 scopus 로고    scopus 로고
    • note
    • Note that the peptide side chain here contains a Gln rather than a Glu residue.
  • 40
  • 47
  • 68
    • 0035943435 scopus 로고    scopus 로고
    • See also, Chiosis
    • See also, Chiosis, G.; Boneea, I. G. Science 2001, 293, 1484. G. Boneea I. G.
    • (2001) Science , vol.293 , pp. 1484
  • 79
    • 14844339524 scopus 로고    scopus 로고
    • For tracing the activity differences between glycopeptide and lipoglycopeptide antibiotics back to a genetic basis, see
    • For tracing the activity differences between glycopeptide and lipoglycopeptide antibiotics back to a genetic basis, see ref 52
    • (2005) Chem. Rev. , vol.105 , pp. 425
    • Kahne, D.1    Leimkuhler, C.2    Lu, W.3    Walsh, C.4
  • 103
    • 15244343393 scopus 로고    scopus 로고
    • For ruthenium-mediated SNAr reactions in synthetic approaches to the ristocetin aglycon, see:
    • For ruthenium-mediated SNAr reactions in synthetic approaches to the ristocetin aglycon, see: Pearson, A. J.; Cui, S. Tetrahedron Lett. 2005, 46, 2639.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 2639
    • Pearson, A.J.1    Cui, S.2
  • 109
    • 0034885143 scopus 로고    scopus 로고
    • and references therein
    • Boger, D. L. Med. Res. Rev. 2001, 21,356 and references therein.
    • (2001) Med. Res. Rev. , vol.21 , pp. 356
    • Boger, D.L.1
  • 110
    • 30744451994 scopus 로고
    • For leading references, see: 4th ed. Helmchen G. Hoffmann R. W. Mulzer J. Schaumann E. Eds.; Thieme: Stuttgart, Germany, New York, 21a (Steroselective Synthesis)
    • For leading references, see: Hartwig, W. In Methodes of Organic Synthesis, 4th ed.; Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann, E., Eds.; Thieme: Stuttgart, Germany, New York, 1995; Vol. E 21a (Steroselective Synthesis), p 1041.
    • (1995) Methodes of Organic Synthesis , vol.E , pp. 1041
    • Hartwig, W.1
  • 117
    • 0033577010 scopus 로고    scopus 로고
    • Thompson, C.; Go, M.; Kahne, D. J. Am. Chem. Soc. 1999, 121, 1237.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 1237
  • 126
    • 0036918754 scopus 로고    scopus 로고
    • and references therein
    • Baltz, R. H. Chem. Biol. 2002, 9, 1268 and references therein.
    • (2002) Chem. Biol. , vol.9 , pp. 1268
    • Baltz, R.H.1
  • 152
    • 14844361787 scopus 로고
    • For semisynthetic analogues with different lipid chains, see:
    • For semisynthetic analogues with different lipid chains, see: (a) Ciabatti, R.; Cavalleri, B. Eur. Patent 337203, 1989;
    • (1989) Eur. Patent 337203
    • Ciabatti, R.1    Cavalleri, B.2
  • 176
    • 23944471937 scopus 로고    scopus 로고
    • Method development for the chemical and enzymatic synthesis of lanthionine-containing peptides has been summarized:
    • Method development for the chemical and enzymatic synthesis of lanthionine-containing peptides has been summarized: Paul, M.; van der Donk, W. A. Mini-Rev. Org. Chem. 2005, 2, 343.
    • (2005) Mini-Rev. Org. Chem. , vol.2 , pp. 343
    • Paul, M.1    van der Donk, W.A.2
  • 179
    • 0000117755 scopus 로고
    • Hahn, F. E., Ed.; Springer: Berlin
    • Huber, G. In Antibiotics; Hahn, F. E., Ed.; Springer: Berlin, 1979; Vol. V/1, pp 135-153.
    • (1979) Antibiotics , vol.5 , Issue.1 , pp. 135-153
    • Huber, G.1
  • 200
    • 0016316948 scopus 로고
    • For a synthesis with low configurational control at the 2,3-double bond (moenocinol numbering), see:
    • For a synthesis with low configurational control at the 2,3-double bond (moenocinol numbering), see: Tschesche, R.; Reden, J. Liebigs Ann. Chem. 1974, 853.
    • (1974) Liebigs Ann. Chem. , pp. 853
    • Tschesche, R.1    Reden, J.2
  • 224
    • 30744440967 scopus 로고    scopus 로고
    • For a recent publication by authors unaware of the previous work, see:
    • For a recent publication by authors unaware of the previous work, see: Arivand, A.; Baskaran, S. Tetrahedron Lett. 2005, 46, 719.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 719
    • Arivand, A.1    Baskaran, S.2
  • 230
  • 236
    • 30744461888 scopus 로고    scopus 로고
    • For preliminary results, see: Dissertation, University of Leipzig
    • For preliminary results, see: Mansourova, M. Dissertation, University of Leipzig, 2002.
    • (2002)
    • Mansourova, M.1
  • 258
    • 0001980840 scopus 로고
    • Preparation of the reagent: and references therein
    • Preparation of the reagent: Jackson, W. P. Synlett 1990, 536 and references therein.
    • (1990) Synlett , pp. 536
    • Jackson, W.P.1
  • 306
    • 0034680096 scopus 로고    scopus 로고
    • Cohen, M. L. Nature 2000, 406, 762-781.
    • (2000) Nature , vol.406 , pp. 762-781
    • Cohen, M.L.1
  • 307
    • 14944375311 scopus 로고    scopus 로고
    • For leading references, see:
    • For leading references, see: Brown, E. D.; Wright, G. D. Chem. Rev. 2005, 105, 759.
    • (2005) Chem. Rev. , vol.105 , pp. 759
    • Brown, E.D.1    Wright, G.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.