会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 4. 发明申请
    • Method for the cultivation of microorganisms of the genus thraustochytriales by using an optimized low salt medium
    • 通过使用优化的低盐培养基培养破囊壶菌属微生物的方法
    • US20070054384A1
    • 2007-03-08
    • US10578968
    • 2004-11-10
    • Matthias RusingMarkus Luy
    • Matthias RusingMarkus Luy
    • C12P7/64C12N1/21A23K1/00
    • C12P7/6427A23K10/37A23L33/12A23V2002/00C12N1/12C12P7/6472
    • The invention relates to an optimized method for cultivating microorganisms of the genus Thraustochytriales, according to which the microorganisms are cultivated in a low salt medium without adding sodium salts and chloride salts, the total salt content being less than 3.5 g/L (corresponding to less than 10 percent of sea water salt content), whereupon the PUFAs are isolated from the microorganisms and/or the medium. The invention especially relates to novel optimized media having a substantially reduced total salt content, above all a particularly reduced NaCl content. The production of PUFAs can be substantially improved and significantly simplified by using a novel combination of different salts as a media composition in which the overall weight ratios of ions do not exceed 1.75 g/L. Furthermore, said medium preferably contains no added sodium salt and chloride salt at all, which helps prevent environmental damages caused by wastewaters containing salt.
    • 本发明涉及一种用于培养破囊壶菌属微生物的优化方法,根据该方法,微生物在低盐培养基中培养而不添加钠盐和氯化物盐,总盐含量小于3.5g / L(相当于少于 超过10%的海水盐含量),由此从微生物和/或介质中分离PUFA。 本发明特别涉及具有显着降低的总盐含量,特别是特别降低的NaCl含量的新型优化的介质。 通过使用不同盐的新型组合作为其中离子的总重量比不超过1.75g / L的介质组合物,可以显着改善和显着地简化PUFA的生产。 此外,所述介质优选根本不含有添加的钠盐和氯化物盐,这有助于防止由含有盐的废水引起的环境损害。
    • 5. 发明授权
    • Process for cultivating microorganisms of the genus Thraustochytriales
    • 培养破囊壶菌属微生物的方法
    • US08889382B2
    • 2014-11-18
    • US10578965
    • 2004-11-10
    • Markus LuyMatthias Rüsing
    • Markus LuyMatthias Rüsing
    • C12P7/64C12N1/00
    • C12P7/6427C12N1/14C12P7/6472
    • The invention relates to an optimized method for the production of PUFAs by cultivating microorganisms belonging to the group of Stramenopiles in a fermentation medium that is pH-stabilized using calcium carbonate and comprises 3-15 g/L CaCO3, whereupon the PUFAs are isolated from the microorganisms and/or the medium. The invention particularly relates to novel optimized media having a different CaCO3 content. By using adequate quantities of CaCO3, the process can be significantly simplified during fermentation while greater quantities of DHA can be obtained at an increased oil content in the biomass. They allow microorganisms belonging to the Stramenopiles to be fermented without controlling the pH, thereby substantially improving and significantly simplifying PUFA production.
    • 本发明涉及通过在使用碳酸钙进行pH稳定化的发酵培养基中培养属于Stramenopiles组的微生物并且包含3-15g / L CaCO 3来生产PUFA的优化方法,由此将PUFA从 微生物和/或培养基。 本发明特别涉及具有不同CaCO3含量的新型优化介质。 通过使用足够量的CaCO 3,可以在发酵期间显着简化该过程,同时在生物质中增加的油含量可获得更多量的DHA。 它们允许属于Stramenopiles的微生物发酵而不控制pH值,从而显着改善和显着简化PUFA生产。
    • 6. 发明授权
    • Screening method for identifying PUFA PKS in samples
    • 用于鉴定样品中PUFA PKS的筛选方法
    • US08409798B2
    • 2013-04-02
    • US11547948
    • 2005-04-08
    • Markus LuyMatthias Rüsing
    • Markus LuyMatthias Rüsing
    • C12Q1/68
    • C12Q1/689
    • The invention relates to a method for the rapid and simple identification of PUFA PKS in microorganisms. Said method is characterized by the fact that DNA sections representing PKS that produce specifically for PUFA (polyunsaturated fatty acids) are reproduced in vitro. The PUFA PKS-specific amino acid sequence LGIDSIKRVEIL makes it possible to derive oligonucleotides which are used for the efficient PCR screening for PUFA PKS genes or PUFA-producing microorganisms. The inventive method is particularly suitable for the high throughput screening of microorganisms for PUFA PKS genes.
    • 本发明涉及用于快速和简单地鉴定微生物中PUFA PKS的方法。 所述方法的特征在于代表PKS产生的专门用于PUFA(多不饱和脂肪酸)的DNA片段在体外再现。 PUFA PKS特异性氨基酸序列LGIDSIKRVEIL可以获得用于有效PCR筛选PUFA PKS基因或产生PUFA的微生物的寡核苷酸。 本发明的方法特别适合用于PUFA PKS基因的微生物的高通量筛选。
    • 9. 发明授权
    • Method for the cultivation of microorganisms of the genus thraustochytriales by using an optimized low salt medium
    • 通过使用优化的低盐培养基培养破囊壶菌属微生物的方法
    • US08900831B2
    • 2014-12-02
    • US10578968
    • 2004-11-10
    • Matthias RüsingMarkus Luy
    • Matthias RüsingMarkus Luy
    • C12P7/64C12N1/00
    • C12P7/6427A23K10/37A23L33/12A23V2002/00C12N1/12C12P7/6472
    • The invention relates to an optimized method for cultivating microorganisms of the genus Thraustochytriales, according to which the microorganisms are cultivated in a low salt medium without adding sodium salts and chloride salts, the total salt content being less than 3.5 g/L (corresponding to less than 10 percent of sea water salt content), whereupon the PUFAs are isolated from the microorganisms and/or the medium. The invention especially relates to novel optimized media having a substantially reduced total salt content, above all a particularly reduced NaCl content. The production of PUFAs can be substantially improved and significantly simplified by using a novel combination of different salts as a media composition in which the overall weight ratios of ions do not exceed 1.75 g/L. Furthermore, said medium preferably contains no added sodium salt and chloride salt at all, which helps prevent environmental damages caused by wastewaters containing salt.
    • 本发明涉及一种用于培养破囊壶菌属微生物的优化方法,根据该方法,微生物在低盐培养基中培养而不添加钠盐和氯化物盐,总盐含量小于3.5g / L(相当于少于 超过10%的海水盐含量),由此从微生物和/或介质中分离PUFA。 本发明特别涉及具有显着降低的总盐含量,特别是特别降低的NaCl含量的新型优化的介质。 通过使用不同盐的新型组合作为其中离子的总重量比不超过1.75g / L的介质组合物,可以显着改善和显着地简化PUFA的生产。 此外,所述介质优选根本不含有添加的钠盐和氯化物盐,这有助于防止由含有盐的废水引起的环境损害。
    • 10. 发明申请
    • Process for cultivating microoraganisms of the genus thraustochytriales
    • 培养破囊壶菌属微阵列反应的方法
    • US20070141686A1
    • 2007-06-21
    • US10578965
    • 2004-11-10
    • Markus LuyMatthias Rusing
    • Markus LuyMatthias Rusing
    • C12P7/62C12N1/21
    • C12P7/6427C12N1/14C12P7/6472
    • The invention relates to an optimized method for the production of PUFAs by cultivating microorganisms belonging to the group of Stramenopiles in a fermentation medium that is pH-stabilized using calcium carbonate and comprises 3-15 g/L CaCO3, whereupon the PUFAs are isolated from the microorganisms and/or the medium. The invention particularly relates to novel optimized media having a different CaCO3 content. By using adequate quantities of CaCO3, the process can be significantly simplified during fermentation while greater quantities of DHA can be obtained at an increased oil content in the biomass. They allow microorganisms belonging to the Stramenopiles to be fermented without controlling the pH, thereby substantially improving and significantly simplifying PUFA production.
    • 本发明涉及通过在使用碳酸钙进行pH稳定化的发酵培养基中培养属于Stramenopiles组的微生物并且包含3-15g / L CaCO 3来生产PUFA的优化方法,由此将PUFA从 微生物和/或培养基。 本发明特别涉及具有不同CaCO3含量的新型优化介质。 通过使用足够量的CaCO 3,可以在发酵期间显着简化该过程,同时在生物质中增加的油含量可获得更多量的DHA。 它们允许属于Stramenopiles的微生物发酵而不控制pH值,从而显着改善和显着简化PUFA生产。