Biosynthesis 1967
DOI: 10.1007/978-3-662-38441-1_21
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Bacitracin, Gramicidin and Tyrocidine

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Cited by 3 publications
(4 citation statements)
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“…Besides the cyclic nature of a molecule, there may be unusual linkages or arrangements of the amino acids in the antibiotic. Bacitracin provides an example, for it possesses a thiazoline ring (derived from the condensation of cysteine and isoleucine), a cyclic hexapeptide, as well as an amide bond between the f3-carboxyl group of aspartic acid and the epsilon amino group of lysine (1,167).…”
Section: Properties Of Peptidementioning
confidence: 99%
See 1 more Smart Citation
“…Besides the cyclic nature of a molecule, there may be unusual linkages or arrangements of the amino acids in the antibiotic. Bacitracin provides an example, for it possesses a thiazoline ring (derived from the condensation of cysteine and isoleucine), a cyclic hexapeptide, as well as an amide bond between the f3-carboxyl group of aspartic acid and the epsilon amino group of lysine (1,167).…”
Section: Properties Of Peptidementioning
confidence: 99%
“…BACITRACINS The bacitracins are synthesized by certain strains ofB. licheniformis (167). Although several bacitracins have been described in the literature, the most completely investigated is bacitracin A (Fig.…”
Section: Ch3 Nh2mentioning
confidence: 99%
“…Bacitracin A, the major and most active component (Galardy, Printz, & Craig, ; Toscano & Storm, ), has a seven‐membered ring, a five amino acid tail, D‐amino acids, ornithine, and a thiazoline ring between the terminal isoleucine and cysteine residues (Figure ). It is active only against Gram positive bacteria (Citron et al, ; Jawetz, , Toscano & Storm, ; Weinberg, )…”
Section: Antimicrobial Peptides Active Against Archaeamentioning
confidence: 99%
“…Bacitracin has multiple modes of action including bacterial membrane lysis (as evidenced by the appearance of rods on plasma membranes using electron microscopy) in the presence of Zn 2+ or Cd 2+ (Sleytr, Oliver, & Thorne, ; Toscano & Storm, ) and inhibition of peptidoglycan synthesis by binding to C 55 ‐isoprenyl pyrophosphate. This binding leads to the formation of a complex which prevents the conversion to the phosphate form leading to inhibition of peptidoglycan biosynthesis (Reynolds, ; Siewert & Strominger, ; Stone & Strominger, ; Storm & Strominger, ; Toscano & Storm, ; Weinberg, , )…”
Section: Antimicrobial Peptides Active Against Archaeamentioning
confidence: 99%