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. Author manuscript; available in PMC: 2011 Mar 1.
Published in final edited form as: Drugs Future. 2010 Mar;35(3):197. doi: 10.1358/dof.2010.035.03.1452077

Table 1.

Antimicrobial peptides that specifically target fungi

Name of the group Representative peptides Origin Structure Mechanism MW1 Susceptible strain References
β-glucan synthase inhibitors Echinocandins
Pneumocandins
Aculeacins
Fungi Cyclic lipopeptides Inhibition of glucan synthesis 1000 Candida spp.
P.carinii
Aspergillus spp
Benz F et al, 1974(47); Fromtling R et al, 1989(50); Iwata K et al, 1982(58)
Mulundocandins Threonine is substituted by serine; and lineoyl with 12- methylmyristoyl Roy K et al, 1987(60); Hawser S et al, 1999(61)
Cell wall chitin inhibitors Nikkomycins
Polyoxins
Bacteria Nucleoside peptide antibiotic Inhibition of chitin synthesis Nikkomycin Z 495 Candida spp.
Coccidiodes immitis
Balstomyces dermatides
Histoplasma capsulatum
McCarthy P et al, (66); Hector R et al, 1990(67)
Aureobasidins Fungi cyclic lipophilic depsipeptide with 8 amino acids and an- hydroxyacid Inhibition of actin and chitin assembly; synthesis of sphingolipids 1100 Candida spp
C. neoformans.
Ikai K et al, 1991(69); Endo M et al, 1997(70); Nagiec M et al, 1997(71)
Membrane-targeting inhibitors Rs-ARF2 Plants α-helical 3-stranded β-sheets, 4 disulphide bridges Target membrane glycosylcerebroside, induces reactive oxygen species, membrane lysis (?) 5730 Candida albicans, C. krusei, A. flavus, Fusarim solani. Schaaper W et al, 2001(76); Thevissen K et al, 2007(73)
Drosomycin Insects α-helical 3-stranded β-sheets, 4 disulphide bridges Target voltage- gated sodium channel (?), Membrane lysis (?) 5250 F. oxysporum
N. crassa
S.cerevisiae
Fehlbaum P et al, 1994(74); Bulet P et al, 2005(276); Yuan Y et al, 2007(277); Cohen L et al, 2009(77)
Bacillomycin F Iturin A Bacteria Cyclic with lipid-soluble β-amino acid linked to the D/L aa Lysis by pore formation and leakage of key ions 1000 Aspergillus niger
C.albicans
F.oxysporum
A. flavus F. moniliforme
Besson F et al, 1984(81) Mhammedi A et al, 1982(82)
Histatins Histatin 1–12 Primates α-helical in hydrophobic environment; increase histidine content Mechanism uncertain (Target mitochondria vs. Trk1 potassium transporter vs lysis of energized membrane) Histatin1: 4880; Histatin 3: 4060; Histatin: 5: 3040 Candida spp. Trichosporon pollulans, Cryptococcus neoformans, A. fumigatus, Pollock J et al, 1984(88); Helmerhorst E et al, 1999(90); Tsai H et al, 1997(91); Baev D et al, 2004(108); Mochon A et al, 2008(105); Troxler R et al, 1990(278)
1

-Approximate molecular weight