1977
DOI: 10.7164/antibiotics.30.297
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Studies on aculeacin. I. Isolation and characterization of aculeacin A.

Abstract: Aculeacin A, a new antifungal antibiotic was isolated from the mycelial cake of Aspergillus aculeatus M-4214. The antibiotic is a white amorphous powder soluble in lower alcohols and hardly soluble in other organic solvents or water. Aculeacin A gave palmitic acid and five ninhydrin-positive products including threonine, hydroxyproline upon acid hydrolysis. The antibiotic showed a potent activity against molds and yeasts, but exhibited no antibacterial activity.

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Cited by 117 publications
(45 citation statements)
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“…These compounds belong to the echinocandin family, a class of antifungal agents that act on the fungal cell wall by inhibiting glucan synthesis. The members of the echinocandin family of fungal origin are FR901379 [14,15], echinocandin B [16], aclueacins [17], mulundocandin [18] and pneumocandins [19], which are produced by C. empetri No. 11899, Aspergillus nidulans, A. aculeatus, A. sydowi and Glarea lozoyensis, respectively.…”
Section: Discussionmentioning
confidence: 99%
“…These compounds belong to the echinocandin family, a class of antifungal agents that act on the fungal cell wall by inhibiting glucan synthesis. The members of the echinocandin family of fungal origin are FR901379 [14,15], echinocandin B [16], aclueacins [17], mulundocandin [18] and pneumocandins [19], which are produced by C. empetri No. 11899, Aspergillus nidulans, A. aculeatus, A. sydowi and Glarea lozoyensis, respectively.…”
Section: Discussionmentioning
confidence: 99%
“…Similarly, aculeacins A to D and F to G have good in vitro activity against Candida spp. and S. cerevisiae and inhibitory though not lethal activity against several filamentous fungi (167,168,211).…”
Section: Inhibitors Of Glucan Synthesismentioning
confidence: 99%
“…The aculeacins, echinocandins, and papulacandins were all discovered as fermentation metabolites during screening programs for new antibiotics. The aculeacins, isolated from Aspergillus aculeatus, were described in 1977 as a complex of seven lipoprotein compounds: aculeacins A, B, C, D, E, F, and G (168,211). Aculeacin A (Fig.…”
Section: Inhibitors Of Glucan Synthesismentioning
confidence: 99%
“…These compounds have similar structures to FR901379 [3,4], the points of difference having different amino acid constituents compared to FR901379 and, most strikingly, a sulphate residue presenting at a different position of the aryl ring. Other related antifungal lipopeptides of fungal origin are FR901379 [3,4], echinocandin B [5] aculeacins [6], mulundocandin [7] and pneumocandins [8,9], which are produced by Coleophoma empetri No. 11899, A. nidulans, A. aculeatus, A. sydowi and Glarea lozoyensis, respectively.…”
Section: Introductionmentioning
confidence: 99%