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Báo cáo nghiên cứu khoa học: Cell suspension culture of Zedoary (Curcuma zedoaria Roscoe)
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VNU Journal of Science, Natural Sciences and Technology 27 (2011) 64-70Vo Chau Tuan1,2, Vu Duc Hoang1, Nguyen Hoang Loc1,*1Institute of Resources, Environment and Biotechnology, Hue University, Hue, Vietnam 2 College of Education, Da Nang University, Da Nang, VietnamReceived 09 June 2010Abstract. Chúng tôi báo cáo ở đây là giao thức cho chai (Curcuma zedoaria Roscoe) Zedoary và các nền văn hóa đình chỉ di động. Môi trường MS có bổ sung sucrose 2%, 1,0 mg / l 2,4-D và 1,0 mg / l BA hiệu quả để cảm ứng chai từ trong ống nghiệm cấy cơ sở lá của Zedoary....
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Báo cáo nghiên cứu khoa học: "Cell suspension culture of Zedoary (Curcuma zedoaria Roscoe)"VNU Journal of Science, Natural Sciences and Technology 27 (2011) 64-70 Cell suspension culture of Zedoary (Curcuma zedoaria Roscoe) Vo Chau Tuan1,2, Vu Duc Hoang1, Nguyen Hoang Loc1,* 1 Institute of Resources, Environment and Biotechnology, Hue University, Hue, Vietnam 2 College of Education, Da Nang University, Da Nang, Vietnam Received 09 June 2010 Abstract. W e report here the protocol for Zedoary (Curcuma zedoaria Roscoe) callus and cell suspension cultures. The MS medium supplemented with 2% sucrose, 1.0 mg/l 2,4-D and 1.0 mg/l BA was effective for callus induction from in vitro leaf-base explants of Zedoary. During subcultures, secondary proliferated calli were subsequently produced from initial induced calli on the MS medium with 0.5 mg/l 2.4-D and 0.5 mg/l BA. These calli were light yellow in color, compact and friable. The cell suspension culture for Zedoary was established using 3 g fresh weight inoculum in a batch culture on the MS medium supplemented with 3% sucrose, 1.5 mg/l 2,4-D and 0.5 mg/l BA. The highest biomass of 10.44 g fresh weight (0.66 g dry weight) was obtained after 14 days of culture in 50 ml liquid medium of 250 ml Erlenmeyer flask with shaking speed of 120 rpm. Results from this study might be a well established foundation for further studies on Curcuma zedoaria Roscoe in order to serve as a potential source for secondary metabolites production in large scale. Keywords: Callus, cell biomass, cell suspension, Curcuma zedoaria, medicinal plant1. Introduction∗ demonstrated antimutagenic activity [2]. It has been also used for stomach diseases, Zedoary (Curcuma zedoaria Roscoe) plant, hepatoprotection [3], treatment of blooda vegetatively propagated species of the stagnation, and promoting menstruation as aZingiberaceae family, is an aromatic traditional medicine in Asia [4]. Furthermore,herbaceous plant with a rhizome growing the Zedoary has anti-inflammatory potencymainly in South Asian and South-East Asian related to its antioxidant effects [3].countries, and China [1]. Zedoary is a valuable Higher plants are a valuable source of widemedicinal plant, the essential oil obtained from range of secondary metabolites, which are usedrhizome has been reported to have antimicrobial as pharmaceuticals, agrochemicals, flavours,activity and be clinically used in the treatment fragrances, colours, biopesticides and foodof cervical cancer, the water extract of Zedoary additives [5]. In the end of 1960s, plant cell culture technologies were introduced as a tool_______ for both studying and producing plant∗ Corresponding author. Tel.: 84-54-6505051. secondary metabolites. A highly potent E-mail: nhloc@hueuni.edu.vn 64 V.C. Tuan et al. / VNU Journal of Science, Natural Sciences and Technology 27 (2011) 64-70 65secondary metabolites that is used in Then, 3 g of cells from initial culture waspharmaceuticals and food additives have been transferred on the MS medium supplementedproduced through plant cell suspension cultures with different plant growth regulators (2,4-Din large-scale [6, 7]. Cell suspension culture is a and BA) and sucrose for investigation ofrequirement for the production of chemicals biomass production. The suspensions werefrom plants in a way quite similar to that used placed on a rotary shaker at 120 rpm for 18for microorganisms, where the utilization of days under the same conditions as for the callus culture except an intensity of 500 lux.bioreactor becomes feasible [8]. The purpose ofthis study is to establish an efficient suspension Samples were obtained every two days tocell culture protocol for C. zedoaria as a determine the cell biomass in both fresh and drystarting point to produce bioactive compounds ...
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Báo cáo nghiên cứu khoa học: "Cell suspension culture of Zedoary (Curcuma zedoaria Roscoe)"VNU Journal of Science, Natural Sciences and Technology 27 (2011) 64-70 Cell suspension culture of Zedoary (Curcuma zedoaria Roscoe) Vo Chau Tuan1,2, Vu Duc Hoang1, Nguyen Hoang Loc1,* 1 Institute of Resources, Environment and Biotechnology, Hue University, Hue, Vietnam 2 College of Education, Da Nang University, Da Nang, Vietnam Received 09 June 2010 Abstract. W e report here the protocol for Zedoary (Curcuma zedoaria Roscoe) callus and cell suspension cultures. The MS medium supplemented with 2% sucrose, 1.0 mg/l 2,4-D and 1.0 mg/l BA was effective for callus induction from in vitro leaf-base explants of Zedoary. During subcultures, secondary proliferated calli were subsequently produced from initial induced calli on the MS medium with 0.5 mg/l 2.4-D and 0.5 mg/l BA. These calli were light yellow in color, compact and friable. The cell suspension culture for Zedoary was established using 3 g fresh weight inoculum in a batch culture on the MS medium supplemented with 3% sucrose, 1.5 mg/l 2,4-D and 0.5 mg/l BA. The highest biomass of 10.44 g fresh weight (0.66 g dry weight) was obtained after 14 days of culture in 50 ml liquid medium of 250 ml Erlenmeyer flask with shaking speed of 120 rpm. Results from this study might be a well established foundation for further studies on Curcuma zedoaria Roscoe in order to serve as a potential source for secondary metabolites production in large scale. Keywords: Callus, cell biomass, cell suspension, Curcuma zedoaria, medicinal plant1. Introduction∗ demonstrated antimutagenic activity [2]. It has been also used for stomach diseases, Zedoary (Curcuma zedoaria Roscoe) plant, hepatoprotection [3], treatment of blooda vegetatively propagated species of the stagnation, and promoting menstruation as aZingiberaceae family, is an aromatic traditional medicine in Asia [4]. Furthermore,herbaceous plant with a rhizome growing the Zedoary has anti-inflammatory potencymainly in South Asian and South-East Asian related to its antioxidant effects [3].countries, and China [1]. Zedoary is a valuable Higher plants are a valuable source of widemedicinal plant, the essential oil obtained from range of secondary metabolites, which are usedrhizome has been reported to have antimicrobial as pharmaceuticals, agrochemicals, flavours,activity and be clinically used in the treatment fragrances, colours, biopesticides and foodof cervical cancer, the water extract of Zedoary additives [5]. In the end of 1960s, plant cell culture technologies were introduced as a tool_______ for both studying and producing plant∗ Corresponding author. Tel.: 84-54-6505051. secondary metabolites. A highly potent E-mail: nhloc@hueuni.edu.vn 64 V.C. Tuan et al. / VNU Journal of Science, Natural Sciences and Technology 27 (2011) 64-70 65secondary metabolites that is used in Then, 3 g of cells from initial culture waspharmaceuticals and food additives have been transferred on the MS medium supplementedproduced through plant cell suspension cultures with different plant growth regulators (2,4-Din large-scale [6, 7]. Cell suspension culture is a and BA) and sucrose for investigation ofrequirement for the production of chemicals biomass production. The suspensions werefrom plants in a way quite similar to that used placed on a rotary shaker at 120 rpm for 18for microorganisms, where the utilization of days under the same conditions as for the callus culture except an intensity of 500 lux.bioreactor becomes feasible [8]. The purpose ofthis study is to establish an efficient suspension Samples were obtained every two days tocell culture protocol for C. zedoaria as a determine the cell biomass in both fresh and drystarting point to produce bioactive compounds ...
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