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    • 55. 发明专利
    • Method for cultivating genetic recombinant microorganism
    • 用于培养遗传重组微生物的方法
    • JPS619282A
    • 1986-01-16
    • JP12747284
    • 1984-06-22
    • Hitachi Ltd
    • SHIMIZU NORIOMASUDA KEIKOKURIHARA TOSHIHARUOTAHARA YOUJI
    • C12N15/09C12N1/20C12N1/21C12N9/38C12N15/00C12R1/19
    • PURPOSE: To obtain efficiently a product of the titled microorganism in a large amount, by cultivating a microorganism having a complex plasmid consisting of the aimed gene, vector and promoter and the expression ability thereof in a culture medium containing an inhibitor substance and an inducer substance to control the promoter activity.
      CONSTITUTION: A microorganism having the aimed gene, vector and promoter in the cell and an expression ability of the aimed gene is cultivated in a culture medium containing an inhibitor substance and inducer substance to control the promoter activity and give the product of the aimed gene efficiently in a large amount. For example, a DNA fragment containing a trp promoter cut out of PTREI is linked to an β-gal gene with an enzyme to create a complex plasmid PTREZI, and tryptophan (trp) is added thereto in the initial period of cultivation to suppress the activity of the trp promoter, reduce the production of the β-gal and multiply the microbial cells. An inducer substance for starting the activity of the trp promoter is then added to produce the β-gal.
      COPYRIGHT: (C)1986,JPO&Japio
    • 目的:通过培养具有目标基因,载体和启动子组成的复合质粒的微生物及其在含有抑制物质和诱导物质的培养基中的表达能力,有效地获得大量标题微生物的产物 以控制启动子活性。 构成:在含有抑制剂物质和诱导物质的培养基中培养具有目的基因,细胞中的载体和启动子和靶基因的表达能力的微生物,以控制启动子活性并有效地产生目的基因的产物 大量的。 例如,含有从PTREI切出的trp启动子的DNA片段与酶的β-gal基因连接以产生复合质粒PTREZI,并且在培养的初始阶段向其中加入色氨酸(trp)以抑制活性 的trp启动子,减少β-gal的产生并繁殖微生物细胞。 然后加入用于启动trp启动子活性的诱导物质以产生β-gal。
    • 56. 发明专利
    • CULTIVATION METHOD OF MICROORGANISM IN HIGH YIELD
    • JPS5898085A
    • 1983-06-10
    • JP19451781
    • 1981-12-04
    • HITACHI LTD
    • MATSUSHITA NOBUOSAIKAI MASAHARUFUJIMOTO MASAKATSUSHIMIZU NORIOUENO MASAO
    • C12M1/36C12N1/00
    • PURPOSE:To cultivate a microorganism in high yield, by measuring the amount of an added pH adjustor, and controlling the feed rate of a substrate on the basis of the amount of the added pH adjustor. CONSTITUTION:The pH a culture medium 25 in the cultivation is controlled to be always at the set value by a pH adjusting apparatus 13, and the rate of change in pH is proportional to the amount of a pH adjustor required for controlling the pH of the culture medium 25 at the set value by adding the pH adjustor from the pH adjusting apparatus 13 to be culture medium 25. Thus, the amount of the pH adjustor added by one opening of a solenoid valve in the pH adjusting apparatus 13 is kept constant, and the amount of the added pH adjustor is determined by multiplying the frequency of addition obtained by integrating the frequencies of the addition of the pH adjustor for a given period by the constant amount of the pH adjustor added to the culture medium 25 on one opening of the solenoid valve in the pH adjusting apparatus 13. The measured amount of the added pH adjustor is calculated by a minicomputer 24 from the operational expression on the basis of the amount of the added pH adjustor to output controlling output signals from the minicomputer 24 to a flow rate variable pump 14 to feed the substrate to the culture medium 25 at a proper rate.
    • 58. 发明专利
    • Cultivation of baker's yeast
    • 空值
    • JPS5736982A
    • 1982-02-27
    • JP11166880
    • 1980-08-15
    • Hitachi Ltd
    • UENO MASAOSHIMIZU NORIOYAMAGUCHI TETSUOSAITO SETSUOOTAHARA YOJI
    • C12N1/00C12N1/16C12N1/18
    • PURPOSE: To control the rate of feeding of substrate in the aerated cultivation of baker's yeast so as to conduct the feed of the cultivation substrate at the optimum rate, by detecting the production of ethanol from the data obtained by the measurement of the feed gas flow and the exhaust gas flow.
      CONSTITUTION: The feed gas flow rate and the exhaust gas flow rate are measured continuously during the cultivation by the feed gas flow meter 5 and the exhaust gas flow meter 6, respectively. The measured data are inputted to a comparing means 7, in which the ratio of the flow rates is calculated, and the comparative relationship of the rates is displayed by the displaying means 8. When the exhaust gas flow rate is larger than the feed gas flow rate, it is supposed that ethanol is produced by the excessive feed of the substrate, and the substrate feed rate is reduced by operating the substrate feed rate controlling means 3. On the contrary, when the exhaust gas flow rate is smaller, the substrate feed rate is incresed. The control can be performed automatically, by electrically connecting the comparing means with the substrate feed rate controlling means.
      COPYRIGHT: (C)1982,JPO&Japio
    • 目的:为了控制面包酵母充气培养中的底物喂养速度,以最佳速率进行培养基质的进料,通过从进料气流测量获得的数据中检测出乙醇的产生 和废气流。 构成:在进料气体流量计5和废气流量计6的培养期间,分别测量进料气体流量和废气流量。 测量数据被输入到比较装置7,在比较装置7中,计算出流量的比率,并通过显示装置8显示速率的比较关系。当废气流量大于进料气体流量 速率,假设通过基板的过量进料产生乙醇,并且通过操作基板进给速率控制装置3来降低基板进给速率。相反,当排气流量较小时,基板进给 价格上涨。 可以通过将比较装置与基板进给速率控制装置电连接来自动执行控制。