Monacrosporium ellipsosporum, a nematode-trapping fungus, was isolated by baiting with sclerotiaof Sclerotinia sclerotiorum in soil from a tobacco field in Yuxi, Yunnan Province. Colonizationfrequency of the scleroti...Monacrosporium ellipsosporum, a nematode-trapping fungus, was isolated by baiting with sclerotiaof Sclerotinia sclerotiorum in soil from a tobacco field in Yuxi, Yunnan Province. Colonizationfrequency of the sclerotia by the fungus was 18% in natural soil. Reinoculation tests byplacing surface-sterilized sclerotia on fungal cultures for two weeks and then surface-sterilized again led to 32% sclerotia be infected. Dual culture tests in PDA plates did notgive rise to a suppression zone between the colonies of M. ellipsosporum and its counterpartfungi S. sclerotiorum and Rhizoctonia solani, suggesting there was little or no nutritionalcompetition and absent of antifungal compounds. However, M. ellipsosporum could grow overabsent of S. sclerotiorum and R. solani, and significantly inhibited their growth on agarplates. Scanning electron and light microscopic observations showed that hyphae of M. ellipsosporumgrew along and appressed on hypha of S. sclerotiorum and coiled around hyphae of R. solani.Assays of cell wall-degrading enzymes showed that M. ellipsosporum grew well in chitin agarmedia, with clear transparent hydrolysis zones. Activities of total chitinase, exo-chitinase,β-1, 3-glucanase and protease were 140.2±11.9, 82.9±4.1, 111.2±7.6 and 76.1±4.3 U respect-ively, after incubation for 4 days at 30 ℃ in liquid media containing ground sclerotia of S.sclerotiorum as sole nutrient source. These enzymes might be important in the mycoparasiticactivity of M. ellipsosporum.展开更多
Chitosan membrane was modified by the selective oxidization of chitosan molecules on its surface with NO2 gas. FTIR spectra indicated there were plenty of –COOH and –COO- groups on the modified membrane surface. The...Chitosan membrane was modified by the selective oxidization of chitosan molecules on its surface with NO2 gas. FTIR spectra indicated there were plenty of –COOH and –COO- groups on the modified membrane surface. The SEM study showed the modified membrane surface was rough rather than smooth as chitosan membrane. All antithrombosis test, hemolysis test and blood cell morphology observation with SEM revealed that modified chitosan membranes have superior blood compatibility to chitosan.展开更多
基金supported by the National High-Tech R&D Proqram(863)of China(2001AA246011).
文摘Monacrosporium ellipsosporum, a nematode-trapping fungus, was isolated by baiting with sclerotiaof Sclerotinia sclerotiorum in soil from a tobacco field in Yuxi, Yunnan Province. Colonizationfrequency of the sclerotia by the fungus was 18% in natural soil. Reinoculation tests byplacing surface-sterilized sclerotia on fungal cultures for two weeks and then surface-sterilized again led to 32% sclerotia be infected. Dual culture tests in PDA plates did notgive rise to a suppression zone between the colonies of M. ellipsosporum and its counterpartfungi S. sclerotiorum and Rhizoctonia solani, suggesting there was little or no nutritionalcompetition and absent of antifungal compounds. However, M. ellipsosporum could grow overabsent of S. sclerotiorum and R. solani, and significantly inhibited their growth on agarplates. Scanning electron and light microscopic observations showed that hyphae of M. ellipsosporumgrew along and appressed on hypha of S. sclerotiorum and coiled around hyphae of R. solani.Assays of cell wall-degrading enzymes showed that M. ellipsosporum grew well in chitin agarmedia, with clear transparent hydrolysis zones. Activities of total chitinase, exo-chitinase,β-1, 3-glucanase and protease were 140.2±11.9, 82.9±4.1, 111.2±7.6 and 76.1±4.3 U respect-ively, after incubation for 4 days at 30 ℃ in liquid media containing ground sclerotia of S.sclerotiorum as sole nutrient source. These enzymes might be important in the mycoparasiticactivity of M. ellipsosporum.
基金Financial support for this work from Natural Science Foundation of Hebei Province(No.B2004000402).
文摘Chitosan membrane was modified by the selective oxidization of chitosan molecules on its surface with NO2 gas. FTIR spectra indicated there were plenty of –COOH and –COO- groups on the modified membrane surface. The SEM study showed the modified membrane surface was rough rather than smooth as chitosan membrane. All antithrombosis test, hemolysis test and blood cell morphology observation with SEM revealed that modified chitosan membranes have superior blood compatibility to chitosan.
