Abstract:
Transacylase enzymes and the use of such enzymes to produce paclitaxel and related taxoids, as well as intermediates in the paclitaxel biosynthetic pathway, are disclosed. Also disclosed are nucleic acid sequences encoding such transacylase enzymes such as (but without limitation) C-13 phenylpropanoid side chain-CoA acyltransferase and benzoyl-CoA:3null-N-debenzoyl-2null-deoxytaxol N-benzoyltransferase.
Abstract:
Oxygenase enzymes and the use of such enzymes to produce paclitaxel (Taxolnull), related taxoids, as well as intermediates in the Taxol biosynthetic pathway are disclosed. Also disclosed are nucleic acid sequences encoding the oxygenase enzymes.
Abstract:
The present invention relates to isolated DNA sequences which code for the expression of plant 1-deoxy-D-xylulose-5-phosphate reductoisomerase protein, such as the sequence presented in SEQ ID NO:1 which encodes a 1-deoxy-D-xylulose-5-phosphate reductoisomerase protein from peppermint (Mentha x piperita). Additionally, the present invention relates to isolated plant 1-deoxy-D-xylulose-5-phosphate reductoisomerase protein. In other aspects, the present invention is directed to replicable recombinant cloning vehicles comprising a nucleic acid sequence which codes for a plant 1-deoxy-D-xylulose-5-phosphate reductoisomerase, to modified host cells transformed, transfected, infected and/or injected with a recombinant cloning vehicle and/or DNA sequence of the invention.
Abstract translation:本发明涉及编码植物1-脱氧-D-木酮糖-5-磷酸还原异构酶蛋白质的表达的分离的DNA序列,例如编码1-脱氧-D-木酮糖的SEQ ID NO:1所示的序列 -5-薄荷薄荷(Mentha x piperita)的5-磷酸还原异构酶蛋白。 另外,本发明涉及分离的植物1-脱氧-D-木酮糖-5-磷酸还原异构酶蛋白。 在其它方面,本发明涉及可复制的重组克隆载体,其包含编码植物1-脱氧-D-木酮糖-5-磷酸还原异构酶的核酸序列转化,转染,感染和/或注射的修饰的宿主细胞 与本发明的重组克隆载体和/或DNA序列。
Abstract:
cDNAs encoding gymnosperm monoterpene synthases have been isolated and sequenced, and the corresponding amino acid sequences have been determined. Modified host cells are provided that have been transformed, transfected, infected and/or injected with a recombinant cloning vehicle and/or DNA sequence encoding a monoterpene synthase of the invention. Thus, systems and methods are provided for the recombinant expression of recombinant monoterpene synthases that may be used to facilitate their production, isolation and purification in significant amounts.
Abstract:
Oxygenase enzymes and the use of such enzymes to produce paclitaxel (Taxolnull) related taxoids, as well as intermediates in the Taxolnull biosynthetic pathway are disclosed. Also disclosed are nucleic acid sequences encoding the oxygenase enzymes. Particular oxygenase enzymes include the disclosed taxoid-14-beta hydroxylases.
Abstract:
Transacylase enzymes and the use of such enzymes to produce paclitaxel and related taxoids, as well as intermediates in the paclitaxel biosynthetic pathway, are disclosed. Also disclosed are nucleic acid sequences encoding such transacylase enzymes such as (but without limitation) C-13 phenylpropanoid side chain-CoA acyltransferase and benzoyl-CoA:3null-N-debenzoyl-2null-deoxytaxol N-benzoyltransferase.
Abstract:
Transacylase enzymes and the use of such enzymes to produce Taxolnull, related taxoids, as well as intermediates in the Taxolnull biosynthetic pathway are disclosed. Also disclosed are nucleic acid sequences encoding the transacylase enzymes.
Abstract:
Transacylase enzymes and the use of such enzymes to produce Taxolnull, related taxoids, as well as intermediates in the Taxolnull biosynthetic pathway are disclosed. Also disclosed are nucleic acid sequences encoding the transacylase enzymes.
Abstract:
A cDNA encoding geranyl diphosphate synthase large subunit from peppermint has been isolated and sequenced, and the corresponding amino acid sequence has been determined. Replicable recombinant cloning vehicles are provided which code for geranyl diphosphate synthase large subunit). In another aspect, modified host cells are provided that have been transformed, transfected, infected and/or injected with a recombinant cloning vehicle and/or DNA sequence encoding geranyl diphosphate synthase large subunit. In yet another aspect, the present invention provides isolated, recombinant geranyl diphosphate synthase protein comprising an isolated, recombinant geranyl diphosphate synthase large subunit protein and an isolated, recombinant geranyl diphosphate synthase small subunit protein. Thus, systems and methods are provided for the recombinant expression of geranyl diphosphate synthase.