[ Objective] The aim was to establish the method of extracting genomic DNA from sheep blood clot on the basis of the improvement of method for extracting genomic DNA from tissues. [Method]The genomic DNA with complete...[ Objective] The aim was to establish the method of extracting genomic DNA from sheep blood clot on the basis of the improvement of method for extracting genomic DNA from tissues. [Method]The genomic DNA with complete primary structure and high purity was obtained from the sheep blood clot after the steps of cutting the sheep blood clot with ophthalmic scissors, cell lysis with tissue DNA extracts and digested by proteinase K, extracting with phenol/chloroform and precipitating with ethanol were performed. [ Result] The concentration of the extracted DNA was 159.90 ±0.70 ng/μl and the ratio of the A260/A280 was 1.80 +0.01. The sheep microsatellite locus of BM203 was amplified by using the extracted DNA from the sheep blood clot as template of PCR, and the PCR result was perfect. [Conclusion]This method is simple and feasible, the quantity and quality of the extracted DNA can satisfy the demands for the subsequent researches. It is worth to extending and using for reference.展开更多
In a completely randomized block design experiment, 16 ruminally cannulated sheep (40 ±2.1 kg)fed a 50% concentrate: 50% forage diet (DM basis) were given intraruminal doses of powdered Yucca schidigera extr...In a completely randomized block design experiment, 16 ruminally cannulated sheep (40 ±2.1 kg)fed a 50% concentrate: 50% forage diet (DM basis) were given intraruminal doses of powdered Yucca schidigera extract (YSE). Doses of 0 (control), 100, 200, or 300 mg kg^-1 diet were given at 8 p.m. and 4 a.m. On 15, 16, and 17 d of the experimental period, ruminal contents were sampled 0, 2, 4, 6, and 8 h after dosing, and blood samples were collected at the end of the experiment (18th and 19th d). Acidity was not affected (P〉0.05) by the addition of YSE. Compared with the control, ruminal propionate concentration was increased by 29.4 and 29.8% (P〉 0.05) and the acetic acid concentration was decreased by 15.1 and 19.8% (P〉0.05) at 4 and 6 h after YSE (300 mg kg^-1) dosing, respectively. Ruminal ammonia concentration in the first 2 h after feeding was higher (P〈0.05) in the sheep that did not receive YSE (increased by 17.57 mg 100 mL^-1) than in those that received 200 mg kg^-1(increased by 6.77 mg 100 mL^-1) or 300 mg kg^-1 (increased by 6.50 mg 100 mL^-1) YSE. Protozoan populations in the rumen were lower (P〈0.05) in the animals that received 300 mg kg^-1 of YSE compared with the control. All serum parameters of the four groups were in the normal range and were similar among the treatment groups (P 〉 0.05), after being fed for 19 d with different doses of YSE. The effect of YSE on ruminal ammonia concentration likely resulted from a decreased concentration of protozoan populations and, presumably, from ammonia binding by YSE.展开更多
[Objective] To analyze the volatile flavor compounds in mutton of different parts of Ningxia Tan sheep. [Method] The volatile flavor compounds in mutton were identified and quantified using the solid phase micro-extra...[Objective] To analyze the volatile flavor compounds in mutton of different parts of Ningxia Tan sheep. [Method] The volatile flavor compounds in mutton were identified and quantified using the solid phase micro-extraction (SPME) method combined with GC-MS analysis. [ Re- sult ] The proportion of aldehydes in volatile compounds was the highest in the mutton of most parts of Ningxia Tan sheep, but no 4-methyl acid and 4-methyl nonyl acid was detected in the mutton. [ Conclusion]Aldehydes may be important for the volatile flavor of mutton of Ningxia Tan sheep. The study provides a basis for better development and use of Ningxia Tan sheep.展开更多
This experiment was conducted in Horticulture Department, School of Plant Production, Faculty of Agriculture and Forestry, University of Duhok, Iraq in 2010 on Chrysanthemum plants, in order to mitigate the adverse in...This experiment was conducted in Horticulture Department, School of Plant Production, Faculty of Agriculture and Forestry, University of Duhok, Iraq in 2010 on Chrysanthemum plants, in order to mitigate the adverse influence of salinity by the use of liquorice root extract and study its effect on vegetative growth, chlorophyll content in leaves from chlorophyll and assistant pigment, carbohydrate and starch. Subsequently, the trail consisted of three levels of salinity (0, 4 and 8 ds m^-1) and three concentrations of the liquorice root extract 0, 2.5 and 5 g L^-1. Results showed that salinity (4 ds m^-1) rate caused significant increases in certain vegetative characteristics (branches number, plant height, leaves number and leaf area), photosynthetic pigments (Chl a, Chl b, total chlorophyll, a-carotene, β-carotene, zeaxanthin, astaxanthin), fresh shoot weight, fresh root weight, shoot dry weight, root dry weight, shoot: root ratio, carbohydrate dry weight percentage and starch percentage as compared to untreated check. However, increasing salinity rate to 8 ds m^-1 resulted in substantial reductions in all above mentioned Waits. Treatment with liquorices root extract, in particular, 5 g L^-1 manifested a potent capability in ameliorating the salinity negative effects in terms of vegetative and photosynthetic pigments aspects.展开更多
基金Supported by Natural Science Foundation of Shanxi Province(2007011081 )Returning Brains Project in Shanxi Province(2007066 )Agricultural Science and Technology Achievement Transformation Fund Project(2008GB2A300032)~~
文摘[ Objective] The aim was to establish the method of extracting genomic DNA from sheep blood clot on the basis of the improvement of method for extracting genomic DNA from tissues. [Method]The genomic DNA with complete primary structure and high purity was obtained from the sheep blood clot after the steps of cutting the sheep blood clot with ophthalmic scissors, cell lysis with tissue DNA extracts and digested by proteinase K, extracting with phenol/chloroform and precipitating with ethanol were performed. [ Result] The concentration of the extracted DNA was 159.90 ±0.70 ng/μl and the ratio of the A260/A280 was 1.80 +0.01. The sheep microsatellite locus of BM203 was amplified by using the extracted DNA from the sheep blood clot as template of PCR, and the PCR result was perfect. [Conclusion]This method is simple and feasible, the quantity and quality of the extracted DNA can satisfy the demands for the subsequent researches. It is worth to extending and using for reference.
文摘In a completely randomized block design experiment, 16 ruminally cannulated sheep (40 ±2.1 kg)fed a 50% concentrate: 50% forage diet (DM basis) were given intraruminal doses of powdered Yucca schidigera extract (YSE). Doses of 0 (control), 100, 200, or 300 mg kg^-1 diet were given at 8 p.m. and 4 a.m. On 15, 16, and 17 d of the experimental period, ruminal contents were sampled 0, 2, 4, 6, and 8 h after dosing, and blood samples were collected at the end of the experiment (18th and 19th d). Acidity was not affected (P〉0.05) by the addition of YSE. Compared with the control, ruminal propionate concentration was increased by 29.4 and 29.8% (P〉 0.05) and the acetic acid concentration was decreased by 15.1 and 19.8% (P〉0.05) at 4 and 6 h after YSE (300 mg kg^-1) dosing, respectively. Ruminal ammonia concentration in the first 2 h after feeding was higher (P〈0.05) in the sheep that did not receive YSE (increased by 17.57 mg 100 mL^-1) than in those that received 200 mg kg^-1(increased by 6.77 mg 100 mL^-1) or 300 mg kg^-1 (increased by 6.50 mg 100 mL^-1) YSE. Protozoan populations in the rumen were lower (P〈0.05) in the animals that received 300 mg kg^-1 of YSE compared with the control. All serum parameters of the four groups were in the normal range and were similar among the treatment groups (P 〉 0.05), after being fed for 19 d with different doses of YSE. The effect of YSE on ruminal ammonia concentration likely resulted from a decreased concentration of protozoan populations and, presumably, from ammonia binding by YSE.
基金funded by the Key Technology R&D Program of Ningxia Hui Autonomous Region
文摘[Objective] To analyze the volatile flavor compounds in mutton of different parts of Ningxia Tan sheep. [Method] The volatile flavor compounds in mutton were identified and quantified using the solid phase micro-extraction (SPME) method combined with GC-MS analysis. [ Re- sult ] The proportion of aldehydes in volatile compounds was the highest in the mutton of most parts of Ningxia Tan sheep, but no 4-methyl acid and 4-methyl nonyl acid was detected in the mutton. [ Conclusion]Aldehydes may be important for the volatile flavor of mutton of Ningxia Tan sheep. The study provides a basis for better development and use of Ningxia Tan sheep.
文摘This experiment was conducted in Horticulture Department, School of Plant Production, Faculty of Agriculture and Forestry, University of Duhok, Iraq in 2010 on Chrysanthemum plants, in order to mitigate the adverse influence of salinity by the use of liquorice root extract and study its effect on vegetative growth, chlorophyll content in leaves from chlorophyll and assistant pigment, carbohydrate and starch. Subsequently, the trail consisted of three levels of salinity (0, 4 and 8 ds m^-1) and three concentrations of the liquorice root extract 0, 2.5 and 5 g L^-1. Results showed that salinity (4 ds m^-1) rate caused significant increases in certain vegetative characteristics (branches number, plant height, leaves number and leaf area), photosynthetic pigments (Chl a, Chl b, total chlorophyll, a-carotene, β-carotene, zeaxanthin, astaxanthin), fresh shoot weight, fresh root weight, shoot dry weight, root dry weight, shoot: root ratio, carbohydrate dry weight percentage and starch percentage as compared to untreated check. However, increasing salinity rate to 8 ds m^-1 resulted in substantial reductions in all above mentioned Waits. Treatment with liquorices root extract, in particular, 5 g L^-1 manifested a potent capability in ameliorating the salinity negative effects in terms of vegetative and photosynthetic pigments aspects.