2013
DOI: 10.3390/molecules18066952
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Novel Biological Activities of Allosamidins

Abstract: Allosamidins, which are secondary metabolites of the Streptomyces species, have chitin-mimic pseudotrisaccharide structures. They bind to catalytic centers of all family 18 chitinases and inhibit their enzymatic activity. Allosamidins have been used as chitinase inhibitors to investigate the physiological roles of chitinases in a variety of organisms. Two prominent biological activities of allosamidins were discovered, where one has anti-asthmatic activity in mammals, while the other has the chitinase-producti… Show more

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Cited by 17 publications
(6 citation statements)
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“…This appears particularly important for the bacterial growth in soil where chitin, mainly originating from insect cuticle and fungal cell walls, is a major nutrient source. Therefore, allosamidin is listed as a potent secondary metabolite with antifungal activity [ 180 ].…”
Section: Streptomycetes In Plant Protection Against Biotic Stressementioning
confidence: 99%
“…This appears particularly important for the bacterial growth in soil where chitin, mainly originating from insect cuticle and fungal cell walls, is a major nutrient source. Therefore, allosamidin is listed as a potent secondary metabolite with antifungal activity [ 180 ].…”
Section: Streptomycetes In Plant Protection Against Biotic Stressementioning
confidence: 99%
“…A set of different molecules from Streptomyces spp. that act against insect pests have been found and characterized; these are, for instance, flavensomycin [194], antimycin A [195], piericidins [196], macrotetralides [197] and prasinons [198]. Streptomyces avermitilis, a common soil inhabitant, was shown to produce avermectins, molecules with potent activity against arthropods and nematodes [199].…”
Section: Streptomycetes In Plant Protection Against Biotic Stressesmentioning
confidence: 99%
“…Allosamidin has a pseudotrisaccharide structure with a β-(1→4) disaccharide of AllNAc residues linked to a five-member cyclitol moiety fused to a dimethylaminooxazoline ring ( Figure 1 ). The fused five-member rings mimic the oxazolinium ion intermediate produced during the hydrolysis of insect family-18 chitinases [ 14 ]. Interestingly, mammals do not have chitin nor chitin synthase activities, but an acidic mammalian chitinase has been described.…”
Section: Introductionmentioning
confidence: 99%