Abstract

Oleanane and ursane pentacyclic triterpenoids are secondary metabolites of plants found in various climatic zones and regions. This group of compounds is highly attractive due to their diverse biological properties and possible use as intermediates in the synthesis of new pharmacologically promising substances. By now, their antiviral, anti-inflammatory, antimicrobial, antitumor, and other activities have been confirmed. In the last decade, methods of microbial synthesis of these compounds and their further biotransformation using microorganisms are gaining much popularity. The present review provides clear evidence that industrial microbiology can be a promising way to obtain valuable pharmacologically active compounds in environmentally friendly conditions without processing huge amounts of plant biomass and using hazardous and expensive chemicals. This review summarizes data on distribution, microbial synthesis, and biological activities of native oleanane and ursane triterpenoids. Much emphasis is put on the processes of microbial transformation of selected oleanane and ursane pentacyclic triterpenoids and on the bioactivity assessment of the obtained derivatives.

Highlights

  • Drugs derived from secondary plant metabolites make up about 25% of the global pharmaceutical market [1]

  • Triterpenoids are secondary metabolites of plants, fungi, marine invertebrates, and algae that are formed during cyclization of an acyclic triterpene squalene [132,133,134,135,136,137,138]

  • This group is most widely represented by compounds of oleanane (OA and glycyrrhetinic acid acid (GA)) and ursane (UA) types, which in large quantities can accumulate in various parts of higher plants [39,41,46]

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Summary

Introduction

Drugs derived from secondary plant metabolites make up about 25% of the global pharmaceutical market [1]. One of the most common ways to increase the effectiveness and bioavailability of triterpenoids is by chemical modification. This usually requires high temperature and pH, use of expensive reagents, and introduction of protective groups of molecule reactive centers [8,9,10,11]. An alternative way to obtain valuable derivatives is by biotransformation under normal and environmentally friendly conditions employing the catalytic activity of microorganisms with high technological stage. 12,246 data on bacterial transformation of oleanane triterpenoids by Streptomyces. The reviews are are overwhelmingly overwhelminglyfocused focusedon onchemical chemicaltransformations transformationsoror describe specific types the reviews describe specific types of of biological activities of triterpenoids Less frequently, they deal with biological transformations.

Distribution
Biosynthesis of of Pentacyclic
Biological Activities of Triterpenic Acids and Their Native Derivatives
Biological Transformation
Fungal Transformation
Bacterial Transformation
Findings
Conclusions
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