Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Preparing heterocyclic carbon compound having only o – n – s,...
Reexamination Certificate
1999-05-13
2002-10-01
Marx, Irene (Department: 1651)
Chemistry: molecular biology and microbiology
Micro-organism, tissue cell culture or enzyme using process...
Preparing heterocyclic carbon compound having only o, n, s,...
C435S189000, C435S117000, C435S118000, C549S510000
Reexamination Certificate
active
06458568
ABSTRACT:
FIELD OF THE INVENTION
The invention relates to a new method for the continuous synthesis of baccatin-III by means of the enzymatic acetylation of 10-deacetyl baccatin-III (10-DAB) in an enzyme reactor.
BACKGROUND OF THE INVENTION
10-DAB and baccatin-III are intermediates for the biosynthesis of taxol and can be isolated in different concentrations from yews (Taxus spec.) (0.0002% of baccatin-III from the bark of
Taxus baccata
, 0.02% of DAB from the needles and branches, Kingston, D.G.I. Pharm. Ther. 1991, 52, 1-34).
Taxans, especially taxol (paclitaxel) are cyclotoxic diterpenes from the yew, of which a few inhibit cell replication on a molecular basis, in that they inhibit growing cells in the G2/M phase of the cell cycle. They therefore have an anti-tumor effect and are used increasingly for the treatment of a series of carcinomas (ovarian, breast, bronchial and lung carcinomas).
Taxans and related active ingredients are produced by plants of the Taxus species and are constituents of different parts of such plants. It is therefore a technically and economically meaningful objective to develop the prerequisites for a rational extraction of taxans (particularly taxol) from Taxus plants and, from this, to derive methods for the recovery of this material and its analogs.
At the present time taxol is obtained on a larger scale by working up the bark of
Taxus brevifolia
Nutt. Extrapolations indicate that about 9 tons of bark have to be worked up in order to produce 1 kg of taxol.
Since this method foreseeably would lead to the destruction of the existing stands of yews, alternatives were sought for obtaining taxol completely or partially by chemical synthesis (Holton, R. A and Ojima, I; EP-A 400971, 1990).
However, because of its complexity, the first-named possibility of obtaining taxol fully by synthesis has foreseeably not proven to be suitable for covering the already existing demand at justifiable costs.
Partial synthesis, starting out from 10-DAB, is more successful. The concentration of 10-DAB in the needles of the European yew (
Taxus baccata
) is about 6 to 10 times that of taxol in the bark of
Taxus breviflora
Nutt. 10-DAB can thus be extracted in larger amounts from a source of raw materials, which can be regenerated.
The purification of 10-DAB is significantly simpler and more economic than the extraction of taxol, since there is no need for the expensive separation of the structurally very similar cephalomannin. Taxol has to be made available in a highly purified form for formulating the drug directly. On the other hand, the purity of 10-DAB only has to be adequate so that it can be used as a starting material for the partial synthesis. Moreover, with 10-DAB, one starts out from a molecule, the complete synthesis is possible only at a cost, which is hardly justifiable economically.
The chemical synthesis of baccatin-III is accomplished successfully by the specific acetylation of the hydroxyl group at position 10 of 10-DAB.
However, it is a disadvantage that the chemical acetylation of the substrate is nonspecific. The four hydroxyl groups in the 10-DAB were shown to have different reactivities in an acetylation reaction. The most reactive one is the C-7 hydroxyl group, followed by the hydroxyl groups at positions C-10 and C-13. On the other hand, the hydroxyl group at C-1 was not acetylated under any of the conditions investigated. Undesirable acetylations at C-7 and C-13 must be prevented by correspondingly expensive chemical blocking of the hydroxyl groups. After a successful acetylation at C-10, the blocking groups must be removed once again.
Basically, the reaction mechanism of the acetyl transferase, isolated from
Taxus baccata
(Zocher, R. Weckerth, W, Hacker, C., Kammer, B., Horbogen, T., Eweld, D., B.B.R.C., 1996, 229, 16-20), that is,
1. The conversion of 10-DAB into baccatin-III outside of the organism is possible (in vitro).
2. The acetyl transferase from
Taxus baccata
is highly specific, that is, the OH group at position C-10 of the 10-DAB substrates is acetylated exclusively (the structures are given in Formulas 1 and 2).
Formula 1: Structure of 10-DAB
Formula 2: Structure of Baccatin-III
There are, however, still some problems with a rational, technical use of the enzyme:
In the case of an enzymatic batch method, the enzyme used is lost during the working up.
The process time of a batch method is of the order of hours.
During longer incubation times, contaminations by microorganisms occurs in the batch method.
Immobilization to improve the technical properties always leads to severe losses in activity.
It was therefore an object of the invention to carry out successfully the enzymatic acetylation of 10-DAB with crude cell extracts from the roots of yews (Taxus spp).
It was therefore a further object of the invention to develop an industrially usable method for the enzymatic synthesis of baccatin-III by the acetylation of 10-DAB, which avoids these disadvantages.
SUMMARY OF THE INVENTION
These objects of the invention are accomplished by a method, in which an aqueous reaction batch is used, which contains a partially purified or a very pure acetyl transferase from the Taxus species and synthesis components, especially 10-DAB, acetyl compounds or optionally an acetyl co-enzyme A, which can be regenerated, and optionally a buffer in solution, and is separated using a semipermeable membrane from an organic solvent, which is used to extract the baccatin-III, the reaction batch being regenerated at regular intervals in an aqueous buffer system and the solvent being changed continuously.
Surprisingly, it was noted that the acetyl transferase, obtained from
Taxus baccata
, is stable even in the presence of organic solvents and that the operational stability of the enzyme is increased drastically, if the aqueous reaction batch, which is in a semipermeable membrane, is surrounded by a suitable organic solvent and regenerated at defined times by dialysis in the aqueous buffer system. The presence of the organic solvent prevents microbial contamination.
DETAILED DESCRIPTION OF THE INVENTION
Accordingly, the methods of the invention provide for the following processes.
the enzymatic acetylation of 10-DAB to form baccatin-III by the acetyl transferase from
Taxus baccata,
the extraction of the baccatin-III, formed in the aqueous batch by enzymatic catalysis, by a suitable organic solvent,
The continuous replacement of the solvent containing the baccatin-III and the continuous removal of the product.
a regeneration of the reaction batch by dialysis in an aqueous buffer system.
Aside from the acetyl transferase, the reaction batch should preferably contain an enzyme for regenerating acetyl coenzyme A (CoA), which activates short-chained fatty acids (acetic acid, propionic acid and acrylic acid), that is, converts them into the acyl CoA thioester.
A system for generating acetyl co-enzyme A (CoA), consists of:
the coenzyme A
the acetyl coenzyme A synthetase or ligase
acetate
a source of energy, namely adenosine-5-triphosphate (ATP), since energy is consumed for activating the fatty acids.
The present method permits the acetyl transferases to be used continuously or semi-continuously for the production of baccatin-III.
The method, for using isotope-labeled acetyl CoA, is very suitable for synthesizing radioactively-labeled baccatin-III.
The preferred variation consists of using acetyl transferases from yews (Taxus species).
It is advantageous if an over-expressed, recombinant acetyl transferase is used as acetyl transferase.
An over-expressed, recombinant acetyl transferase is the enzyme, which is used in a reaction batch and has been produced by genetic engineering methods in an organism, which differs from the Taxus species, for example, in a fungus or a yeast.
The dialysis or semipermeable membrane is permeable for the reaction products but not for the enzyme. Preferably, it consists of a cellulose ester.
The dialysis or semipermeable membrane is surrounded by a suitable organic solvent. All solvents, in which the product is soluble and which form two-pha
Glund Konrad
Hoffmann Matthias
Weckwerth Wolfram
Zocher Rainer
Institut fuer Bioanalytik, Umwelt-Toxikologie und Biotechnologie
Jordan and Hamburg LLP
Marx Irene
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