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    • 5. 发明授权
    • Biosynthesis of polyketides
    • US11781120B2
    • 2023-10-10
    • US16930220
    • 2020-07-15
    • Ramon Gonzalez
    • Ramon GonzalezSeokjung CheongJames M. Clomburg
    • C12N9/10C12P15/00C12P17/06
    • C12N9/1025C12P17/06C12Y203/01174
    • This disclosure generally relates to the use of microorganisms to make various functionalized polyketides through polyketoacyl-CoA thiolase-catalyzed non-decarboxylative condensation reactions instead of decarboxylative reactions catalyzed by polyketide synthases. Native or engineered polyketoacyl-CoA thiolases catalyze the non-decarboxylative Claisen condensation in an iterative manner (i.e. multiple rounds) between two either unsubstituted or functionalized ketoacyl-CoAs (and polyketoacyl-CoAs) serving as the primers and acyl-CoAs serving as the extender unit to generate (and elongate) polyketoacyl-CoAs. Before the next round of polyketoacyl-CoA thiolase reaction, the β-keto group of the polyketide chain of polyketoacyl-CoA can be reduced and modified step-wise by 3-OH-polyketoacyl-CoA dehydrogenase or polyketoenoyl-CoA hydratase or polyketoenoyl-CoA reductase. Dehydrogenase converts the β-keto group to β-hydroxy group. Hydratase converts the β-hydroxy group to α-β-double-bond. Reductase converts the α-β-double-bond to single bond. Spontaneous or thioesterase catalyzed termination reaction terminates the elongation of polyketide chain of polyketoacyl-CoA at any point through CoA removal and spontaneous reactions rearrange the structure, generating the final functional polyketide products.
    • 9. 发明授权
    • Anaerobic fermentation of glycerol
    • 甘油的厌氧发酵
    • US08334119B2
    • 2012-12-18
    • US13347811
    • 2012-01-11
    • Ramon Gonzalez
    • Ramon Gonzalez
    • C12P7/00
    • C12P7/065C12P3/00C12P7/40Y02E50/17
    • The invention relates to the development of appropriate cultivation conditions for a bacteria to grow anaerobically (fermentatively) on a glycerol substrate. The method requires culturing bacteria having a functional 1,2-propanediol pathway and a functional type II glycerol dehydrogenase-dihydroxyacetone kinase pathway in a culture medium containing high concentrations of glycerol, a neutral to mildly acidic pII, low levels of potassium and phosphate, and high levels of CO2, such that glycerol is thus converted into a desirable product, such as ethanol, hydrogen, formate, succinate, or 1,2-propanediol.
    • 本发明涉及在甘油底物上厌氧生长(发酵)培养细菌的合适培养条件。 该方法需要在含有高浓度甘油,中性至轻度酸性pII,低水平钾和磷酸盐的培养基中培养具有官能1,2-丙二醇途径和功能性II型甘油脱氢酶 - 二羟基丙酮激酶途径的细菌,以及 高水平的CO 2,使得甘油因此转化为所需的产物,例如乙醇,氢气,甲酸盐,琥珀酸盐或1,2-丙二醇。