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Inhibitory Effects of Cysteine and Cysteine Derivatives on Germination of Sporangiospores and Hyphal Growth of Different Zygomycetes

机译:半胱氨酸和半胱氨酸衍生物对孢子囊孢子萌发和不同合子菌菌丝生长的抑制作用

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The in vitro antifungal activity of cysteine (d- and l-cysteine) and its four derivatives (l-cysteine-methyl-ester, N-acetyl-cysteine, N-isobutyryl-d-cysteine, and N-isobutyryl-l-cysteine) were investigated on 20 fungal isolates representing 16 genera (Absidia, Actinomucor, Backusella, Gilbertella, Micromucor, Mortierella, Mucor, Mycotypha, Phycomyces, Rhizomucor, Rhizopus, Saksenaea, Syncephalastrum, Thamnostylum, Umbellopsis, and Zygorynchus). The inhibitory potential of different concentrations of these compounds, ranging from 0.625 to 10 mM, were investigated on the germination of sporangiospores as well as on hyphal extension, using broth microdilution method and agar plate test. Treatment with cysteine and its derivatives resulted in a strong inhibition in most studied strains. At 10 mM of compounds, complete blockage of growth was observed for some isolates. Sensitive species exhibited severe changes in colony morphology in the presence of 10 mM l-cysteine, N-acetyl-cysteine, and N-isobutyryl-l-cysteine. Microscopic observations revealed that 10 mM N-acetyl-cysteine induced dramatic modifications in the structural organization of the hyphae. Results suggest that cysteine and its derivatives have a therapeutic potential against fungal infections caused by Zygomycetes species.
机译:半胱氨酸(d-和l-半胱氨酸)及其四个衍生物(l-半胱氨酸甲酯,N-乙酰半胱氨酸,N-异丁酰基-d-半胱氨酸和N-异丁酰基-1-半胱氨酸)的体外抗真菌活性)在代表16个属的20个真菌分离株上进行了调查(Absidia,Actinomucor,Backusella,Gilbertella,Micromucor,Mortierella,Mucor,Mycotypha,Phycomyces,Rhizomucor,Rhizopus,Saksenaea,Syncephalastrum,Thamnostylum,Umbellopsis和Zygorynchus)。使用肉汤微稀释法和琼脂平板试验研究了不同浓度的这些化合物在0.625至10 mM范围内对孢子囊孢子萌发以及菌丝延伸的抑制潜力。在大多数研究的菌株中,用半胱氨酸及其衍生物进行的处理均具有较强的抑制作用。在10 mM的化合物下,观察到某些分离株的生长被完全阻断。在10 mM 1-半胱氨酸,N-乙酰半胱氨酸和N-异丁酰基-1-半胱氨酸的存在下,敏感物种的菌落形态发生了严重变化。显微镜观察发现10 mM N-乙酰半胱氨酸在菌丝的结构组织中引起了显着的变化。结果表明,半胱氨酸及其衍生物具有针对由合酶菌属物种引起的真菌感染的治疗潜力。

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