Nystatin is a polyene antifurgal drug to which many molds and yeasts are sersitive, including cryptococcus neoformans, candida, aspergillus, etc. To realize the mechanism of nystatin more particularly, the techniques ...Nystatin is a polyene antifurgal drug to which many molds and yeasts are sersitive, including cryptococcus neoformans, candida, aspergillus, etc. To realize the mechanism of nystatin more particularly, the techniques of SPR and impedance were used to investigate the interaction between nystatin and two kinds of solid-supported phospholipid membranes. The results show that nystatin could interact with pure phospholipid membranes, whether they are monolayer or bilayer. In addition, impedance spectra show that ion channels may be formed when nystatin interacted with phospholipid membranes.展开更多
Neomycins are a group of aminoglycoside antibiotics with both clinical and agricultural applications.To elucidate the regulatory mechanism of neomycin biosynthesis,we completed draft genome sequencing of a neomycin pr...Neomycins are a group of aminoglycoside antibiotics with both clinical and agricultural applications.To elucidate the regulatory mechanism of neomycin biosynthesis,we completed draft genome sequencing of a neomycin producer Streptomyces fradiae CGMCC 4.7387 from marine sediments,and the neomycin biosynthesis gene cluster was identified.Inactivation of the afsA-g gene encoding a γ-butyrolactone(GBL) synthase in S.fradiae CGMCC 4.7387 resulted in a significant decrease of neomycin production.Quantitative RT-PCR analysis revealed that the transcriptional level of neoR and the aphA-neoGH operon were reduced in the afsA-g::aac(3)Ⅳ mutant.Interestingly,a conserved binding site of AdpA,a key activator in the GBL regulatory cascade,was discovered upstream of neoR,a putative regulatory gene encoding a protein with an ATPase domain and a tetratricopeptide repeat domain.When neoR was inactivated,the neomycin production was reduced about 40%in comparison with the WT strain.Quantitative RT-PCR analysis revealed that the transcriptional levels of genes in the aphA-neoGH operon were reduced clearly in the neoR::aac(3)Ⅳ mutant.Finally,the titers of neomycin were improved considerably by overexpression of qfsA-gand neoR in S.fradiae CGMCC 4.7387.展开更多
文摘Nystatin is a polyene antifurgal drug to which many molds and yeasts are sersitive, including cryptococcus neoformans, candida, aspergillus, etc. To realize the mechanism of nystatin more particularly, the techniques of SPR and impedance were used to investigate the interaction between nystatin and two kinds of solid-supported phospholipid membranes. The results show that nystatin could interact with pure phospholipid membranes, whether they are monolayer or bilayer. In addition, impedance spectra show that ion channels may be formed when nystatin interacted with phospholipid membranes.
基金funded in part by the Ministry of Science and Technology of China(2015CB150600)the National Natural Science Foundation of China(31370095 and 31522001)
文摘Neomycins are a group of aminoglycoside antibiotics with both clinical and agricultural applications.To elucidate the regulatory mechanism of neomycin biosynthesis,we completed draft genome sequencing of a neomycin producer Streptomyces fradiae CGMCC 4.7387 from marine sediments,and the neomycin biosynthesis gene cluster was identified.Inactivation of the afsA-g gene encoding a γ-butyrolactone(GBL) synthase in S.fradiae CGMCC 4.7387 resulted in a significant decrease of neomycin production.Quantitative RT-PCR analysis revealed that the transcriptional level of neoR and the aphA-neoGH operon were reduced in the afsA-g::aac(3)Ⅳ mutant.Interestingly,a conserved binding site of AdpA,a key activator in the GBL regulatory cascade,was discovered upstream of neoR,a putative regulatory gene encoding a protein with an ATPase domain and a tetratricopeptide repeat domain.When neoR was inactivated,the neomycin production was reduced about 40%in comparison with the WT strain.Quantitative RT-PCR analysis revealed that the transcriptional levels of genes in the aphA-neoGH operon were reduced clearly in the neoR::aac(3)Ⅳ mutant.Finally,the titers of neomycin were improved considerably by overexpression of qfsA-gand neoR in S.fradiae CGMCC 4.7387.
