Objective:To undertake a study on prevalence of Deg Nala disease in eastern states of India and to reproduce the disease in buffaloes by the Fusarium spp.,isolated from the affected region. Methods:During this investi...Objective:To undertake a study on prevalence of Deg Nala disease in eastern states of India and to reproduce the disease in buffaloes by the Fusarium spp.,isolated from the affected region. Methods:During this investigation,a survey was conducted covering four states of eastern region to identify the Deg Nala cases as well as to isolate and characterize the causative agent(s). An experimental study was carried out to reproduce the disease in healthy male buffaloes(2-3 years age) by randomly dividing them into five groups(four in each group).Each individual group was fed with rice straw artificially infested with either of the two representative isolates of Fusarium oxysporum(F.oxysporum)(F01,F02) or representative reference strains of Fusarium equiseti(F.equiseti)(ITCCF-2470) and Fusarium moniliforme(F.moniliforme)(ITCCF-4821) for 30 days,whereas the control group was fed with normal rice straw only.Results:A total of 658 Deg Nala cases were recorded and 12 Fusarium isolates were identified from the mouldy rice straw collected from these affected areas.The characterization of the isolates revealed three species viz.,F.oxysporum,F.equiseti and F.moniliforme,among which F.oxysporum was predominant.The disease was artificially reproduced in three buffaloes in F01 group and one in F02 group within 20-23 days by feeding F.oxysporum infested rice straw which resembled the clinical symptoms and gross lesions of natural Deg Nala cases.Conclusions:The field investigation and laboratory studies,including experimental production of Deg Nala disease suggest the possible involvement of mycotoxins.However,further investigations needs to be done to understand nature of the toxic factors involved in production of the Deg Nala disease.展开更多
The Synechocystis sp. PCC 6803 genome harbours a Deg gene family consisting of three members, htrA （degP, slr1204）, hhoA （degQ, sll1679） and hhoB （degS, sll1427）. This work provided biochemical characterization ...The Synechocystis sp. PCC 6803 genome harbours a Deg gene family consisting of three members, htrA （degP, slr1204）, hhoA （degQ, sll1679） and hhoB （degS, sll1427）. This work provided biochemical characterization of HhoA, HtrA and HhoB from Synechocystis sp. PCC 6803. Firstly mature HhoA, HhoB and HtrA from Synechocystis sp. PCC 6803 were cloned and expressed as soluble recombinant his-tagged fusion protein in Escherichia coli. Then the proteolytic activity of HhoA, HhoB and HtrA was tested using casein, bovine serum albumin, five recombinant chromoproteins and cyanobacterial phycocyanin as substrates in vitro. The experimental results showed that HhoA and HtrA had proteolytic activity on casein, five recombinant chromoproteins and cyanobacterial phycocyanin. No proteolytic activity of HhoB was found using all substrates in vitro, indicating functional difference among Deg proteases from Synechocystis sp. PCC 6803. Therefore, the results indicated the biochemical properties of HhoA and HtrA on hydrolysis of proteins and phycobiliproteins in vitro, which implicated that they were proteases possibly involved in phycobiliprotein degradation in vivo.展开更多
This study provided a new configuration of the 180-deg round turned channel with a perforated divider, as well as numerically investigated the effect of perforations, including the diameter of perforation and the ange...This study provided a new configuration of the 180-deg round turned channel with a perforated divider, as well as numerically investigated the effect of perforations, including the diameter of perforation and the angel of perforation, on the fluid flow and heat transfer. The numerical results appeared in good agreement with previous experimental data under the same operating conditions. The results indicated that large size and positive angle of perforation changed the fluid flow pattern and the local Nusselt-number distribution fundamentally. It is noteworthy that a more uniform distribution of Nusselt-number was achieved by increasing the diameter of perforation.展开更多
文摘Objective:To undertake a study on prevalence of Deg Nala disease in eastern states of India and to reproduce the disease in buffaloes by the Fusarium spp.,isolated from the affected region. Methods:During this investigation,a survey was conducted covering four states of eastern region to identify the Deg Nala cases as well as to isolate and characterize the causative agent(s). An experimental study was carried out to reproduce the disease in healthy male buffaloes(2-3 years age) by randomly dividing them into five groups(four in each group).Each individual group was fed with rice straw artificially infested with either of the two representative isolates of Fusarium oxysporum(F.oxysporum)(F01,F02) or representative reference strains of Fusarium equiseti(F.equiseti)(ITCCF-2470) and Fusarium moniliforme(F.moniliforme)(ITCCF-4821) for 30 days,whereas the control group was fed with normal rice straw only.Results:A total of 658 Deg Nala cases were recorded and 12 Fusarium isolates were identified from the mouldy rice straw collected from these affected areas.The characterization of the isolates revealed three species viz.,F.oxysporum,F.equiseti and F.moniliforme,among which F.oxysporum was predominant.The disease was artificially reproduced in three buffaloes in F01 group and one in F02 group within 20-23 days by feeding F.oxysporum infested rice straw which resembled the clinical symptoms and gross lesions of natural Deg Nala cases.Conclusions:The field investigation and laboratory studies,including experimental production of Deg Nala disease suggest the possible involvement of mycotoxins.However,further investigations needs to be done to understand nature of the toxic factors involved in production of the Deg Nala disease.
基金Funded by the National Natural Science Foundation of China (Nos.30870541,30870519)
文摘The Synechocystis sp. PCC 6803 genome harbours a Deg gene family consisting of three members, htrA （degP, slr1204）, hhoA （degQ, sll1679） and hhoB （degS, sll1427）. This work provided biochemical characterization of HhoA, HtrA and HhoB from Synechocystis sp. PCC 6803. Firstly mature HhoA, HhoB and HtrA from Synechocystis sp. PCC 6803 were cloned and expressed as soluble recombinant his-tagged fusion protein in Escherichia coli. Then the proteolytic activity of HhoA, HhoB and HtrA was tested using casein, bovine serum albumin, five recombinant chromoproteins and cyanobacterial phycocyanin as substrates in vitro. The experimental results showed that HhoA and HtrA had proteolytic activity on casein, five recombinant chromoproteins and cyanobacterial phycocyanin. No proteolytic activity of HhoB was found using all substrates in vitro, indicating functional difference among Deg proteases from Synechocystis sp. PCC 6803. Therefore, the results indicated the biochemical properties of HhoA and HtrA on hydrolysis of proteins and phycobiliproteins in vitro, which implicated that they were proteases possibly involved in phycobiliprotein degradation in vivo.
文摘This study provided a new configuration of the 180-deg round turned channel with a perforated divider, as well as numerically investigated the effect of perforations, including the diameter of perforation and the angel of perforation, on the fluid flow and heat transfer. The numerical results appeared in good agreement with previous experimental data under the same operating conditions. The results indicated that large size and positive angle of perforation changed the fluid flow pattern and the local Nusselt-number distribution fundamentally. It is noteworthy that a more uniform distribution of Nusselt-number was achieved by increasing the diameter of perforation.
