A brief outline of the research project for Meshack Afitlhile,
a Ph.D. candidate in Plant Physiology/Biochemistry/Molecular Biology
program
My research concerns control of oxylipin formation. Oxylipins are a
diverse class of oxygenated fatty acid derivatives with roles in plant
growth and development, pest resistance and quality of food products. Some
oxylipins are also high value industrial chemical feedstocks. Oxylipin
formation is thought to be initiated by specific lipases which release
free fatty acids (FFAs) from membrane lipids. FFAs are subsequently acted
upon by lipoxygenases (LOXs) and then by hydroperoxide lyase (HPL), allene
oxide synthase (AOS) and/or peroxygenase, generating volatile 6-carbon
aldehydes, jasmonic acid (JA), and epoxy/hydroxy fatty acids,
respectively.
6-carbon aldehydes and alcohols such as hexanal, trans-2-hexenal and
cis-3-hexenol are associated with 'green odors' of leaves and are
important components of the aroma and flavor of many food and beverage
products. These volatile compounds are lost during the production process
such as canning or drying. As a result, there is interest in the food
industry for the natural production of these compounds so as to be used in
food and beverage flavorings. These compounds are also associated with
off-odor and off-flavor of soybean products. Thus, some of the 6-carbon
aldehydes are thought to have antimicrobial properties. Normally, 6-carbon
aldehydes and alcohols are undetectable in undamaged plant tissues except
from fruits and flowers.
JA and its methyl ester, methyl-jasmonate (JAMe) are involved in signal
transduction in response to wounding and pest attack. JA and/or JAMe can
induce proteinase inhibitors in plants, which can be important in pest
resistance.
Members of the Artemisia species are of economic use. Artemisia
afra is a medicinal herb (it is used to treat coughs, colds and flu,
as well as intestinal ailments) in South Africa. A. absinthium and
A. camphorata are moth and insect repellents, respectively. In
China, A. annua and A. vulgaris are used to treat malaria
and asthma, respectively. A. dracunculus is used for maximizing
food flavor.
Our research with these plants is not directly geared towards the
understanding of their medicinal value, but rather the oxylipin pathway
which is thought to give flavor and aroma to food, as well as conferring
resistance to pests.
Our preliminary data have shown that species of Artemisia produce a
high level of JA and JAMe, as well as 6-carbon aldehydes from crushed
leaves. In addition, these plant species seem to have comparable level of
esterified and free fatty acids. JA/JAMe, 6-carbon aldehydes and fatty
acids were analyzed by Gas Chromatography (GC-FID detector), and their
identity confirmed by Gas Chromatography-Mass Spectrometry (GC-MS).
The overall goal of this research project is to understand the regulation
of JA/JAME and 6-carbon aldehyde formation in Artemisia species.
This will be achieved by:
- feeding [U-14C] linolenic acid (18:3) to plant tissues and
monitor its conversion to JA and 6-carbon aldehydes, and
- examine step(s) representing key regulatory points in the formation of
JA and 6-carbon aldehydes
Knowledge acquired from these studies will be used to facilitate
production of transgenic plants with increased and controlled formation of
these compounds for improved agricultural food and industrial use.
Cited References
Farmer, E. E. and Ryan, C. A. (1990) Interplant
communication: Airborne methyl jasmonate induces synthesis of
proteinase inhibitors in plant leaves. PNAS 87: 7713-7716
Gardner, H. W. (1989) How lipoxygenase pathway affects the
organoleptic properties of fresh fruit and vegetables. In D. B. Min
and T. H. Smouse, eds. Flavor Chemistry of Lipid Foods. Am. Oil
Chemists Soc., Champaign, IL, pp. 98-112
Hamberg, M. and Gardner, H. W. (1992) Oxylipin pathway to
jasmonates: Biochemistry and Biological Significance.
Biochem. Biophys. Acta 1165: 1-8
Hatanaka, A., Kajiwara, T. and Sekiya, J. (1987) Biosynthetic
pathway for 6-carbon aldehyde formation from linolenic acid in green
leaves. Chem. Phys. Lipids 44: 341-361
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