Micro-biology Procedure
  Home  Link to us  Resources  Site map  Search  Language

Index >> Industrial Microbiology >> Steriods Translations in Pharmaceutical Industry

Steriods Translations in Pharmaceutical Industry

Steroids Translation in Pharmaceutical Industry - Microbial biotransformation of steroids is very important in the pharmaceutical industry. Steroids are used in treatment of various-disorders and also involved in regulation of sexuality. Chemical synthesis of steroids is very complex because of the requirement to achieve the necessary precision of substituent location.

For example cortisone can be synthesised chemically from deoxycholic acid but the process requires 37 steps, many of which must be carried out under extreme conditions of temperature and pressure with the resulting product costing over $200 per gram. The most difficult is introduction of oxygen atom at number 11 position of the steroid ring, but this can be accomplished by some microorganisms. The fungus, Rhizopus nigricans for example hydroxylates progesterone, forming another steroid with the introduction of oxygen at the number 11 position.

The fungus Cunninghamella blakesleeana similarily can hydroxylate the steroid cortexolone to form hydrocortisone with the introduction of oxygen at number 11 position. Other transformations of the steroid nucleus carried out by microbes include hydrogenations, dehydrogenations, epoxidations and removal and addition of the side chains.

The use of such microbial biotransformations in the formation of cortisone has lowered the original cost over 400-fold, so that in 1980 the price of cortisone in the U.S. was less than 50 cents per gram, compared to the original $200.

In a typical steroid transformation process, the microbe, such as Rhizopus nigricans is grown in a fermentation tank using an appropriate growth medium and incubation conditions to achieve a high biomass. In most cases agitation and aeration are done to have rapid growth.

After the growth of the microbe, the steroid to be transformed is added (as progesterone here) to the fermentor containing R.nigricans that has been growing for one day or so and the steroid is hydroxylated at number 11 to form 11-α- hydroxyprogesterone.

Product is recovered by extraction with methylene chloride or other solvents, purified chromatographically and recovered by crystallization. A large number of similar transformations are carried out to produce a great variety of steroid derivatives for different medicinal uses

Home | Site map | Submit Article | Resources | Search