The Journal of Antibiotics
Online ISSN : 1881-1469
Print ISSN : 0021-8820
ISSN-L : 0021-8820
XYLOCANDIN: A NEW COMPLEX OF ANTIFUNGAL PEPTIDES
II. STRUCTURAL STUDIES AND CHEMICAL MODIFICATIONS
GREGORY S. BISACCHIDEBORAH R. HOCKSTEINWILLIAM H. KOSTERWILLIAM L. PARKERMARLENE L. RATHNUMSTEVE E. UNGER
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JOURNAL FREE ACCESS

1987 Volume 40 Issue 11 Pages 1520-1529

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Abstract
Xylocandins A1, A2, B1, B2, C1, C2, D1 and D2 are new antifungal peptides isolated from Pseudomonas cepacia ATCC 39277. The molecular weights of the xylocandins were determined by fast atom bombardment mass spectrometry (A1 m/z 1, 215; A2 1, 199; B1 1, 229; B2 1, 213; C1 1, 097; C2 1, 081; D1 1, 083; D2 1, 067). Each xylocandin is a cyclic peptide containing glycine (1), serine (2), asparagine (1 - 3 residues), β-hydroxytyrosine (1), and an unusual amino acid with the formula C18H37NO5 (1). Additionally A1, A2, D1 and D2 contain 2, 4-diaminobutyric acid (1); A1, B1, C1 and D1 contain erythro-β-hydroxyasparagine (1); and A1, A2, B1 and B2 contain xylose (1). For each xylocandin pair, an erythro-β-hydroxyasparagine residue in the first component of the pair is thus replaced by an asparagine in the second component, accounting for the 16 dalton mass difference for each pair. Chemical modification of A1 and A2 at the diaminobutyric acid and β-hydroxytyrosine residues was used to probe structural requirements for activity.
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