Microbial 11.alpha.-hydroxylation of steroids

Abstract

The invention relates to a microbial method of in vitro transformation of a steroid into its corresponding 11.alpha.-hydroxy analogue using oxygen and a microorganism selected from the Aspergillus ochraceus, Aspergillus niger, Rhizopus stolonifer, Rhizopus nigricans, Rhizopus arrhizus, and strains of Pestelotia, using as substrate a steroid having a purity of less than 97% and more than 90% at a concentration greater than 10 g/l.

Description

FIELD OF THE INVENTION

The present invention relates to a microbial method of 11.alpha.-hydroxylation of steroids.

BACKGROUND OF THE INVENTION

Microbial 11.alpha.-hydroxylation of steroids is a well known process, in vivo as well as in vitro. For instance 11.alpha.-hydroxylation of progesterone by cell-free preparations of Aspergillus ochraceus has been reported by Shibahara et al., Biochim. Biophys. Acta, 202 (1970), 172-179. It has also been known that microbial 11.alpha.-hydroxylation reactions of steroids are unpredictable, and invariably lead to incomplete transformations. Typically conversion degrees of 80-85% are obtained. For industrial applications it is however of importance to obtain high predictable conversion rates, which preferably lead to higher than 95% yields of 11.alpha.-hydroxylated steroids. Mathematical models in the optimization of such fermentation processes are discussed by Deshayes et al., Bull. Soc. Chim. Fr., (1980), II 24-34. For example, in the 11.alpha.-hydroxylation of canrenone, Deshayes disclosed that under optimum conditions better than 95% yields could be attained when Aspergillus ochraceus was used in a medium containing i.a. 10 g/l of glucose in a matrix of malt-extract and trypticase. Under these conditions up to 1.5 g/l of canrenone could be transformed, which was considered to be an improvement in the art, for instance as disclosed by Blunt et al., J. Chem. Soc., 6 (1971), 1136, who were not able to obtain more than 90% yield of 11.alpha.-hydroxylated canrenone using at the most 0.5 g/l of substrate.

SUMMARY OF THE INVENTION

Since it can be reasoned that contaminations will have a detrimental influence on the microbial process, it can be expected that further optimization could be obtained by increasing the purity of the starting materials. Surprisingly however, it has now been found that a further improvement is obtained by using less than pure substrate, in particular by using a substrate having a purity of less than 97%. The invention therefore relates to a microbial method of in vitro transformation of a steroid into its corresponding 11.alpha.-hydroxy analogue using oxygen and a micro-organism selected from Aspergillus ochraceus, Aspergillus niger, Rhizopus stolonifer, Rhizopus nigricans, Rhizopus arrhizus, and strains of Pestelotia, characterized in that a steroid having a purity of less than 97% is used.

Preferably the microorganism is Aspergillus ochraceus. The purity of the steroid is preferably more than 90%. More preferably the purity of the steroid is between 90 and 95%. The present method using impure substrates affords microbial transformations at substrate concentrations, which are substantially greater than the maximum concentrations as disclosed by blunt or Deshayes.

DETAILED OF DESCRIPTION OF THE INVENTION

The present microbial method can be used with steroids having an unsubstituted 11-position. Preferred examples are estr-4-ene-3,17-dione and canrenone.

The surprising effect of impurities on the conversion degree is illustrated in the following tables.

TABLE I______________________________________Conversion of estr-4-ene-3,17-dione by A. ochraceus purity substrate concentration conversion degree (%) (g/l) (%)______________________________________ 99 15 78 99 10 83 98 25 85 94* 15 91 94* 15 91 94* 15 94 93 25 97 92 10 98______________________________________ *various natural impurities added to pure substrate TABLE II______________________________________Conversion of canrenone by A. ochraceuis purity substrate concentration conversiondegree (%) (g/1) (%)______________________________________100 5 74 100 10 78 100 20 73 100 35 72 96 10 98 94 15 96 96 22 96 95 22 95______________________________________ The invention is further illustrated by the following examples.

EXAMPLES

Example 1

A shake flask containing a mineral growth medium with glucose was inoculated with spores of A. ochraceus and placed on a reciprocal shaker at 28.degree. C. for 15 h. A stirred fermentor containing 5 l of medium was subsequently inoculated with 250 ml of germinated spore suspension. The used medium contained a glucose/yeast extract medium (glucose 40 g/l, yeast extract 10 g/l, pH 5.0). The culture conditions were as follows: stirrer speed 750 rpm, airflow 0.2 l/l/m, temp 28.degree. C. Foaming was measured with an antifoam electrode and controlled by automatic addition of a silicon based antifoam agent. When the culture had a biomass concentration of at least 2 g/l a small portion of estr-4-ene-3,17-dione (1 g/l) was added to induce the synthesis of the hydroxylation enzymes. Three hours later higher concentrations of steroid were added to reach the desired concentrations as given in Table I. The steroid transformation was stopped when repeatedly no increase in conversion was observed.

Example 2

In a shake flask the same culture as described in Example 1 was prepared. When the culture had a biomass concentration of at least 4 g/l the canrenone was added at once to reach the desired concentrations as given in Table II. The steroid transformation was stopped when repeatedly no increase in conversion was observed.

Claims

1. In a microbial method of in vitro transformation of a steroid selected from estr-4-ene-3,17-dione and canrenone into its corresponding 11.alpha.-hydroxy analogue using oxygen and a microorganism selected from the Aspergillus ochraceus, Aspergillus niger,, Rhizopus stolonifer, Rhizopus nigricans, Rhizopus arrhizus, and strains of Pestelotia, the improvement comprising using as substrate a steroid having a purity of less than 97% and more than 90% at a concentration greater than 10 g/l.

2. The method according to claim 1, wherein the microorganism is Aspergillus ochraceus.

3. The method according to claim 1, wherein the purity of the steroid is between 90 and 95%.

4. The method according to claim 2, wherein the purity of the steroid is between 90 and 95%.