[ Objective ] The aim of this study is to identify 6 marine fungi species by analyzing ITS nucleotide sequence, which had been primarily identified as penicillium based on morphological characteristics. [ Method ] The...[ Objective ] The aim of this study is to identify 6 marine fungi species by analyzing ITS nucleotide sequence, which had been primarily identified as penicillium based on morphological characteristics. [ Method ] The ITS regions of these species were cloned by molecule biology method and phylogenetic analyzed using ClustalX1.83 software. [ Result] The ITS regions of these species were sequenced, and phylogenetic analysis between the yield sequences and the ITS sequences assessed in GenBank showed that the 6 strains all belonged to penicillium. [ Condusion] The present study suggests ITS sequence analysis could not be used as an only proof, but it is a very useful supplementary tool for the classification and identification of marine peniciUium combined with morphological characteristics.展开更多
Abstract Ergosterol,（1→3）-α-D-glucan and chitosan are important biomaterials. In this research, a process has been developed to integratively extract ergosterol, （1→3）-α-D-glucan, and chitosan from Penicillium...Abstract Ergosterol,（1→3）-α-D-glucan and chitosan are important biomaterials. In this research, a process has been developed to integratively extract ergosterol, （1→3）-α-D-glucan, and chitosan from Penicillium chrysongenum mycelium. First the mycelia are pretreated with 0.1mol·L^-1 of NaOH. After recovery by centrifugation the solid portion is made to undergo saponification and deacetylation reactaons by addition of 2mol·L^-1 NaOH and et anol.After reaction, extraction is carried out by addition of petroleum ether, which separates the reaction mixture into two phases. The upper layer of petroleum ether contains extracted ergosterol, and the .bottom layer of NaOH solution contains （1→3）-α-DEglucan; the chitosan is on the mycelia residuum. After isolation, the recovery yield of ergosterol is 0.52% of dry mycelium. That of （1→3）-α-D-glucan is about 8.2%; and chitosan is 5.7% with 86% deacetylation. The compositions have been characterized by 1R, HPLC analyses.展开更多
The water extract of dry mycelium ofPenicillium chrysogenum （DME） was used to induce resistance in Virginia tobacco plants against Phtophthora parasitica var. nicotianae. Results showed that the efficacy of DME in c...The water extract of dry mycelium ofPenicillium chrysogenum （DME） was used to induce resistance in Virginia tobacco plants against Phtophthora parasitica var. nicotianae. Results showed that the efficacy of DME in controlling black shank disease depended on both DME solution concentration and its＇ treatment methodology. Soil application of 1.5-5% DME 72 hr before inoculation with Phtophthora parasitica vat. nicotianae provided highly significant protection against black shank, relative to the control without DME treatment. Optimized tobacco plant treatment with 2.5% DME significantly increased peroxidase （POD） and polyphenol oxidase （PPO） activity levels in the upper leaf sections of the tobacco plants. DME had no direct antifungal activity on the growth of Phtophthora parasitica var. nicotianae in vitro, suggesting that disease control with DME treatment resulted from the induced propagation of natural defense mechanisms in the tobacco plants.展开更多
基金Supported by Standardization Arrangement and Integration and Shareof the Offshore Ocean Microorganism Resources(2004DKA30640)~~
文摘[ Objective ] The aim of this study is to identify 6 marine fungi species by analyzing ITS nucleotide sequence, which had been primarily identified as penicillium based on morphological characteristics. [ Method ] The ITS regions of these species were cloned by molecule biology method and phylogenetic analyzed using ClustalX1.83 software. [ Result] The ITS regions of these species were sequenced, and phylogenetic analysis between the yield sequences and the ITS sequences assessed in GenBank showed that the 6 strains all belonged to penicillium. [ Condusion] The present study suggests ITS sequence analysis could not be used as an only proof, but it is a very useful supplementary tool for the classification and identification of marine peniciUium combined with morphological characteristics.
基金Supported by the National Natural Science Foundation of China （No.20636010, No.50373003, No.20406002）, Beijing Natural Science Foundation （No.2071002）, and the Special Funds for Major State Basic Research Program of China （973 Program, No.2007CB714305）.
文摘Abstract Ergosterol,（1→3）-α-D-glucan and chitosan are important biomaterials. In this research, a process has been developed to integratively extract ergosterol, （1→3）-α-D-glucan, and chitosan from Penicillium chrysongenum mycelium. First the mycelia are pretreated with 0.1mol·L^-1 of NaOH. After recovery by centrifugation the solid portion is made to undergo saponification and deacetylation reactaons by addition of 2mol·L^-1 NaOH and et anol.After reaction, extraction is carried out by addition of petroleum ether, which separates the reaction mixture into two phases. The upper layer of petroleum ether contains extracted ergosterol, and the .bottom layer of NaOH solution contains （1→3）-α-DEglucan; the chitosan is on the mycelia residuum. After isolation, the recovery yield of ergosterol is 0.52% of dry mycelium. That of （1→3）-α-D-glucan is about 8.2%; and chitosan is 5.7% with 86% deacetylation. The compositions have been characterized by 1R, HPLC analyses.
文摘The water extract of dry mycelium ofPenicillium chrysogenum （DME） was used to induce resistance in Virginia tobacco plants against Phtophthora parasitica var. nicotianae. Results showed that the efficacy of DME in controlling black shank disease depended on both DME solution concentration and its＇ treatment methodology. Soil application of 1.5-5% DME 72 hr before inoculation with Phtophthora parasitica vat. nicotianae provided highly significant protection against black shank, relative to the control without DME treatment. Optimized tobacco plant treatment with 2.5% DME significantly increased peroxidase （POD） and polyphenol oxidase （PPO） activity levels in the upper leaf sections of the tobacco plants. DME had no direct antifungal activity on the growth of Phtophthora parasitica var. nicotianae in vitro, suggesting that disease control with DME treatment resulted from the induced propagation of natural defense mechanisms in the tobacco plants.
