Received 11 June 2023;
Revised 11 September
2023; Accepted 29
September 2023
Bioproducts from the microbial metabolization of terpenes
SHORT COMMUNICATION
Ana Flávia Seraine Custódio Viana and Boris Timah Acha
Medicinal Plants Research Center, Health Sciences Center, Federal University of Piauí, Teresina, Brazil
This paper explores the potential of microbial biotransformation as a sustainable and cost-effective
method for generating valuable bioproducts from terpenes, essential components of many
plant-derived oils. Terpenes and terpenoids, comprising a diverse group of organic compounds,
exhibit various pharmacological activities with applications in pharmaceuticals, cosmetics, and food
industries. Traditional chemical extraction methods for obtaining terpenes are often expensive and
environmentally unsustainable. In contrast, microbial biotransformation offers an attractive
alternative by utilizing biological catalysts to produce complex terpenoid compounds, which are
often more biologically active and less toxic. The paper discusses the enzymatic pathways involved in
terpene biosynthesis and highlights recent advancements in microbial biotransformation
techniques. Additionally, the paper discusses the potential of recombinant microorganism strains in
large-scale production of bioactive terpenes, addressing challenges associated with traditional
extraction methods. Overall, this paper underscores the significance of microbial biotransformation
in unlocking the therapeutic potential of terpenes and terpenoids, paving the way for the
development of novel bioproducts with enhanced pharmacological activities and reduced
environmental impact.
ABSTRACT
Terpenes; Terpenoids;
Microbial
biotransformation;
Pharmacological activity;
Sustainable production;
Bioproducts
KEYWORDS
ARTICLE HISTORY
© 2023 The Author(s). Published by Reseapro Journals. This is an Open Access article distributed under the terms of the Creative Commons Attribution License
(http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
*Correspondence: Dr. Ana Flávia Seraine Custódio Viana, Department of Physiology and Pharmacology, Federal University of Piauí, Teresina, Brazil, e-mail:
flavia_seraine@hotmail.com
Essential oils are highly concentrated hydrophobic mixtures of
aromatic volatile substances derived from plants, which also
contain more than 300 organic compounds, such as alkaloids,
flavonoids, saponins, and terpenes. ey are widely used as
flavoring agents by the cosmetic and food industries,
respectively. e growing interest of the pharmaceutical
industry in essential oils has stimulated pharmacological
research in these chemicals that have already demonstrated
relevant therapeutic properties such as antimicrobial, antiviral,
anthelmintic, antioxidant, anti-inflammatory, insecticidal,
larvicidal, immunomodulatory, antinociceptive, and anti-ulcer
activities [1].
Some chemical components of essential oils, such as
terpenes and terpenoids, which are organic compounds, have
been constantly investigated and have shown various
pharmacological effects. But what is the difference between
terpenes and terpenoids? Terpenes are a large group of
compounds with simple hydrocarbons. e isoprene unit, a
five-carbon branched chain, gives rise to the different types of
terpenes, which include hemiterpenes, (C10) monoterpenes,
(C15) sesquiterpenes, (C20) diterpenes, (C30) triterpenes, and
(C40) tetraterpenes. Monoterpenes are the most predominant
constituents of essential oils. Examples of bioactive
monoterpenes are limonene, myrcene, ocimene, menthane, and
α-phellandrene, etc. Terpenoids are classified as alcohols,
aldehydes, esters, ethers, epoxides, ketones, and phenols
because they have an oxygen molecule in their structure.
Examples of bioactive terpenoids include carvacrol, linalool,
linalyl acetate, menthol, thymol, and myrtenol. Terpenes and
terpenoids are produced naturally by the mevalonic acid
pathway in the cytoplasm of eukaryotic cells or by the
methylerythritol phosphate (MEP) pathway in the cytoplasm of
eubacteria [2].
Chemical methods to extract large amounts of terpenes
from essential oils are considered expensive because of the
need for structured chemical laboratories with
High-performance liquid chromatography (HPLC) apparatus
to isolate and purify these products. In addition, an exorbitant
amount of plant material is required to obtain a good amount
of essential oil and its constituents. is implies the risk of
extinguishing the plant or species, as it occurred when
paclitaxel (a chemotherapeutic agent) was extracted from the
yew plant (Taxus baccata). Due to the difficulty in obtaining
significant quantities of taxol, it was necessary to collect many
barks of this plant species, which was used in an unsustainable
way, and now it is at risk of extinction in the Pacific [3].
In recent years, the pharmaceutical and chemical industry
has recognized biotransformation as an important alternative,
where biological catalysts facilitate or even make possible the
production of complex by-products, such as terpenoids.
Biotransformers make the reaction more specific and
eliminate the need for purification that is required in chemical
extraction methods. In addition, the use of microbial cells, for
example, filamentous fungi, as biotransforming agents is
easier and cheaper than using purified enzymes [4].
us, biotransformation is considered an economical and
ecologically viable technology. Some studies have shown that
the biotransformation of bioactive substances generates more
biologically active products with reduced toxicity, such as
cyclic monoterpenes with antimicrobial potential. Aſter
biotransformation, the bioproducts have low molecular
weight and more potent antimicrobial activity. Monoterpenes
with antioxidant, anti-inflammatory, and antimicrobial
activity are valuable raw materials for the pharmaceutical
industry. However, large-scale production of these
compounds is very costly [5]. Currently, biotechnology has
JOURNAL OF PLANT RESEARCH AND INNOVATIONS
2023, VOL. 1, ISSUE 1, pp. 1-2
https://doi.org/10.61577/jpri.2023.100001