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Review
. 2012 Feb 24;17(3):2367-77.
doi: 10.3390/molecules17032367.

Beauvericin, a bioactive compound produced by fungi: a short review

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Review

Beauvericin, a bioactive compound produced by fungi: a short review

Qinggui Wang et al. Molecules. .

Abstract

Beauvericin is a cyclic hexadepsipeptide mycotoxin, which has insecticidal, antimicrobial, antiviral and cytotoxic activities. It is a potential agent for pesticides and medicines. This paper reviews the bioactivity, fermentation and biosynthesis of the fungal product beauvericin.

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Figures

Figure 1
Figure 1
Beauvericin structure.
Figure 2
Figure 2
Mechanism of beauvericin cytotoxicity to a human leukemia cell (*beauvericin induced extracellular Ca2+ movement into the cell resulting in an increase in the level of intracellular Ca2+; dashed arrows indicate the specific mechanisms that are unclear).
Figure 3
Figure 3
A, Beauvericin biosynthesis pathway; B, The specific substeps of the key step (formula image represents the beauvericin synthetase; the dashed frame indicates the key step of beauvericin synthesis); C, The possible structure of the beauvericin synthetase (E1 is the D-HYIV module; E2 is the L-Phe module; SH1,2,3 are the 4'-phosphopantetheine residues corresponding to D-HYIV, L-Phe, and the linear hexadepsipeptide acceptor; M is the N-methyltransferase domain; Cy is the cyclization cavity).

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References

    1. Hamill R.L., Higgens G.E., Boaz H.E., Gorman M. The structure of beauvericin, a new desipeptide antibiotic toxic to Artemia salina. Tetrahedron Lett. 1969;49:4255–4258.
    1. Logrieco A., Moretti A., Castella G., Kostecki M., Golinski P., Ritieni A., Chelkowski J. Beauvericin Production by Fusarium Species. Appl. Environ. Microb. 1998;64:3084–3088. - PMC - PubMed
    1. Grove J.F., Pople M. The insecticidal activity of beauvericin and the enniatin complex. Mycopathologia. 1980;70:103–105. doi: 10.1007/BF00443075. - DOI
    1. Shin C.G., An D.G., Song H.H., Lee C. Beauvericin and enniatins H, I and MK1688 are new potent inhibitors of human immunodeficiency virus type-1 integrase. J. Antibiot. 2009;62:687–690. doi: 10.1038/ja.2009.102. - DOI - PubMed
    1. Champlin F.R., Grula E.A. Noninvolvement of beauvericin in the entomopathogenicity of Beauveria bassiana. Appl. Environ. Microb. 1979;37:1122–1126. - PMC - PubMed

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