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1.MethodsThe optimized host cell,culture medium and induction time were deternined according to the growth and expression specificity of nrhTNF on test tube and flask shaker. Then fed batch culture was carried out on 5 L automatic fermentor.
方法通过探讨nrhTNF工程菌在试管和锥形摇瓶中的生长和表达规律 ,筛选并确定其最适宿主菌、最佳培养基及最佳诱导表达条件 ,然后在 5L自控发酵罐中进行分批补料培养。收藏指正
2.Main items are travel mug, vacuum flask, PC bottle, PE bottle, aluminum bottle, hip flask, coffee pot, lunch jar, martin shaker, etc.
产品主要有汽车杯,保温瓶,PC瓶,PE瓶,铝瓶,酒壶,咖啡壶,饭盒,摇酒器等。收藏指正
3.5.0×10 8 spores were inoculated in 250 mL Erlenmeyer flask containing 50 mL medium with a water shaker (120 r/min,32℃) stirring for 5 days.
接种量为 5 .0× 10 8个孢子 / 5 0mL培养基 ,振荡培养 (12 0r/min) 5d收藏指正
4.They were inoculated into a 250ml Erlenmeyer flask containing 50 ml of the media with Ca 3(PO 4) 2 or organophorus pesticide as the only phosphorus source. The flasks were cultivated on a rotary shaker at 30℃ for 4 days under agitation of 180 r/min, then phosphorus in the medium were measured by different methods.
实验分别以Ca3(PO4)2、氧化乐果和水胺硫磷为唯一磷源,接种4株菌,在30℃、180rmin条件培养4d后,以钼蓝比色法测上清液中的水溶性磷含量。收藏指正
5.The optimal culture conditions were as follows: lactose 3.5%, sodium nitrate 3.0%, K2HPO4 0.05%, MgSO4·7H2O 0.025%, KCl 0.05%, FeSO4·7H2O 0.001%, temperature 26℃, initial pH 8.0, shaker rotate speed 150 rpm, volume loading 60 mL of 250 mL Erlenmeyer flask.
工艺条件为:温度26℃、摇床转速150 rpm、起始pH 8.0和装液量60 mL/250 mL,发酵周期为14天。收藏指正
6.The optimum conditions were as follows:the 300mL Erlenmeyer flask containing 150mL of liquid medium was inoculated with 7.5mL of mycelial fragments and the medium was supplied with lignin at a concentration of 0.1%(initial pH8.5). The cultures was incubated at 28℃ on rotary shaker(150r/min) for 4~5 days. The maximum enzyme activity was 20184IU/L.
应用添加有 1g/LKraft木素的液体发酵培养基 ,接种量 5 %(V/V) ,初始pH8 5 ,装液量为 5 0 %,2 8℃、 1 5 0r/min摇瓶振荡培养 4~ 5d ,漆酶酶活水平达 2 0 1 84IU/L。收藏指正
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