Current
Position
- Faculty,
Department
of
Chemistry
and
Biochemistry
Education
and
Training
2000-2004
Postdoctoral
Research
Fellow
University
of Saskatchewan,
Dept.
of Chemistry,
Saskatoon,
Saskatchewan,
Canada
1996-1999
Doctorat
Sciences
des
Agroressources
Institut
National
Polytechnique
de Toulouse,
École
Nationale
Supérieure
de Chimie
de Toulouse,
Dept.
des
sciences
pharmaceutiques,
Université
Toulouse
III,
Toulouse,
France
1995-1996
DEA
Sciences
des
Agroressources
Institut
National
Polytechnique
de Toulouse,
École
Nationale
Supérieure
de Chimie
de Toulouse,
Dept.
des
sciences
pharmaceutiques,
Université
Toulouse
III,
Toulouse,
France
1991-1995
Maîtrise
Chimie
et Biologie
Végétales
Université
de Pau
et des
Pays
de l’Adour,
Faculté
des
Sciences
et Techniques,
Pau,
France
Research
Funding
- Laurentian
University
Start-up
funds
- Laurentian
University
Institutional
Research
Funds
- Natural
Sciences
and
Engineering
Research
Council
of
Canada
(Discovery
grant
–
Individual
and
Research
Tools
and
Instruments
-
Category
1)
- Ministry
of
Northern
Development
and
Mines
Lab
Staff
Research
Investigations
Cancer
chemopreventive
and
antioxidants
natural
products
from
glucosinolate
containing
plants
Our
group
is interested
in natural
product
chemistry.
Our
research
interests
are
mainly
oriented
toward
the
isolation
and
structure
elucidation
of secondary
metabolites
from
higher
plants
using
modern
spectroscopic
methods.
We preferably
focus
on new
natural
products
likely
to possess
biological
activities.
1.
Originally,
we are
more
concerned
about
the
plants
from
the
Brassicaceae
family
or also
called
Crucifers,
which
are
mainly
consumed
as vegetables.
The
most
famous
examples
belonging
to that
family
of cruciferous
plants
are
cabbages,
canola,
cauliflower,
radishes
etc.
Several
epidemiological
studies
suggest
that
consumption
of cruciferous
vegetables
may
be particularly
effective
in reducing
cancer
risk
at several
organ
sites.
Crucifers
that
are
widely
consumed
are
especially
rich
in glucosinolates,
which
are
responsible
for
the
hot,
pungent
taste
of the
mustards.
Glucosinolates
are
beta-thioglucoside
N-hydroxysulfates
with
a side
chain
and
a sulphur-linked
beta-D-glucopyranose
moiety,
which
are
converted
by plant
myrosinase
and
gastrointestinal
microflora
to isothiocyanates.
A limited
number
of glucosinolates
that
were
examined
effectively
block
chemical
carcinogenesis
in animal
models.
2.
Fruits
and
vegetables
contain
several
polyphenolic
compounds,
which
possess
in general
several
biological
properties.
Flavonoids
are
mainly
used
as veinotonic.
They
have
anti-inflammatory
as well
as anti-allergic
properties.
Some
of them
have
shown
cytotoxic,
antimitotic,
antitumor
and
potential
cancer
chemopreventive
activities.
Furthermore,
some
polyphenolic
compounds
(for
example
proantocyanidins
from
grape
and
wine)
have
antioxidant
activities
and
they
could
possess
a role
in enhancing
chemoprevention
and
prolonging
healthy
life.
In fact,
in spite
of a
lipid
rich
diet,
the
low
impact
on cardiovascular
diseases
called
the
French
paradox
is assigned
to red
wine
consumption.
Multiple
mechanisms
are
undoubtedly
involved
in the
protective
effects
of diets
rich
in fruits
and
vegetables.
We
are
investigating
the
phytochemical
compositions
(intact
glucosinolates
and
their
hydrolysis
products,
flavonoids,
alkaloids…)
of wild
cruciferous
plants
that
have
never
been
studied
in general
and
for
potential
cancer
chemoprotection
or antioxidants
properties.
These
studies
will
be performed
on various
wild
cruciferous
plants
but
also
endemic
plants
of Canada.
These
investigations
can
be expanded
to other
glucosinolates
containing
families
and
other
plant
families
especially
to species
used
in different
folk
medicines.
The
compounds
will
be separated
using
several
chromatographic
methods.
After
structural
elucidation,
quantification
in different
organs
of the
plants,
pure
compounds
could
be used
in more
elaborated
tests
to understand
the
mechanisms
of action.
The
objective
is to
develop
new
perspectives
of uses
for
these
plants,
which
would
give
them
a higher
value
in addition
to food
consumption
and
to have
a better
understanding
of the
relative
contributions
of various
components
of plants
to cancer
risk
reduction.
Refereed
Papers
M.
Soledade
C. Pedras,
Mohamed
Hossain,
Mohamed
G. Sarwar
and
Sabine
Montaut.
Determination
of the
enantiomeric
purity
of the
phytoalexins
spirobrassinins
by 1H
NMR
using
chiral
solvation.
Bioorg.
Med.
Chem.
Lett.,
14,
5469-5471,
2004.
M. Soledade
C. Pedras,
Sabine
Montaut
and
Mojmír
Suchý.
Phytoalexins
from
the
crucifer
rutabaga:
structures,
synthesis,
biosynthesis
and
antifungal
activites.
J. Org.
Chem.,
69,
4471-4476,
2004.
M.
Soledade
C. Pedras
and
Sabine
Montaut.
The
biosynthesis
of crucifer
phytoalexins:
unprecedented
incorporation
of a
1-methoxyindolyl
precursor.
Chem.
Comm.,
4, 452-453,
2004.
M.
Soledade
C. Pedras,
Sabine
Montaut,
Irina
L. Zaharia,
Yuanzu
Gai
and
Dale
E. Ward.
Transformation
of the
host-selective
toxin
destruxin
B by
wild
crucifers:
probing
a detoxification
pathway.
Phytochemistry,
64(5),
957-963,
2003.
M.
Soledade
C. Pedras
and
Sabine
Montaut.
Probing
crucial
metabolic
pathways
in fungal
pathogens
of crucifers:
biotransformation
of indole-3-acetaldoxime,
4-hydroxyphenylacetaldoxime,
and
their
metabolites.
Bioorg.
Med.
Chem.,
11,
3115-3120,
2003.
M.
Soledade
C. Pedras,
Corwin
M. Nycholat,
Sabine
Montaut,
Yiming
Xu and
Abdul
Q. Khan.
Chemical
defenses
of crucifers:
elicitation
and
metabolism
of phytoalexins
and
indole-3-acetonitrile
in brown
mustard
and
turnip.
Phytochemistry
59,
611-625,
2002.
Antoine
Fréchard,
Nicolas
Fabre,
Christophe
Péan,
Sabine
Montaut,
Marie-Thérèse
Fauvel,
Patrick
Rollin
and
Isabelle
Fourasté.
Corrigendum
to «
Novel
indole-type
glucosinolates
from
woad
(Isatis
tinctoria
L.)”.
Tetrahedron
Lett.,
43,
1591-1592,
2002.
Antoine
Fréchard,
Nicolas
Fabre,
Christophe
Péan,
Sabine
Montaut,
Marie-Thérèse
Fauvel,
Patrick
Rollin
and
Isabelle
Fourasté.
Novel
indole-type
glucosinolates
from
woad
(Isatis
tinctoria
L.).
Tetrahedron
Lett.,
42,
9015-9017,
2001.
M.
Soledade
C. Pedras,
Sabine
Montaut,
Yiming
Xu,
Abdul
Q. Khan
and
Ali
Loukaci.
Assembling
the
biosynthetic
puzzle
of crucifer
metabolites:
indole-3-acetaldoxime
is incorporated
efficiently
into
phytoalexins
but
glucobrassicin
is not.
Chem.
Comm.,
17,
1572-1573,
2001.
Non-refereed
contributions
Sabine
Montaut.
Chemical
Defenses
of Cultivated
Cruciferous
Plants:
Structure,
Activity
and
Biosynthetic
Precursors.
Northeastern
Ontario
Regional
Cancer
Centre,
Department
of Research
(Sudbury,
Canada).
December
13th
2004.
Invited
presentation.
Sabine
Montaut.
Phytoalexins
in Cruciferous
Vegetables
- Turnip,
Rutabaga
and
Kohlrabi:
Isolation,
Structure
Determination
and
Biosynthesis.
Laurentian
University,
Department
of Chemistry
&
Biochemistry
(Canada).
June
15th
2004.
Invited
presentation.
Sabine
Montaut
and
M. Soledade
C. Pedras.
Phytoalexins
from
the
crucifer
rutabaga:
isolation,
structure
determination,
and
biosynthesis.
39th
IUPAC
Congress
and
86th
Canadian
Society
for
Chemistry
(CSC)
Conference
and
Exhibition,
August
10-15th
2003,
Ottawa
(Canada).
Poster
N°OR.7.P082
(298).
M.
Soledade
C. Pedras,
Sabine
Montaut,
Paulos
B. Chumala
and
Pearson
W. K.
Ahiahonu.
Phytoalexins
from
Wild
and
Cultivated
Crucifers:
Isolation,
Structure
Determination,
Synthesis,
and
Biosynthesis.
38th
National
Organic
Chemistry
Symposium,
June
8-12th
2003,
Bloomington,
Indiana
(U.S.A).
Poster
N°D38.
Sabine
Montaut.
Phytoalexins
in Cruciferous
Vegetables:
Crucial
Role
of Indole-3-acetaldoxime
in Biosynthesis.
University
of Saskatchewan,
Department
of Chemistry
(Canada).
March
4th
2003.
Invited
presentation.
M.
Soledade
C. Pedras,
Sabine
Montaut,
Paulos
B. Chumala
and
Pearson
W.K.
Ahiahonu.
Chemical
Defenses
of Crucifers:
Biotransformation
and
Biosynthesis.
23rdInternational
Symposium
on the
chemistry
of natural
products,
July
28th-August
2nd
2002,
Florence,
Italy.
Presentation
O14.
M.
Soledade
C. Pedras
and
Sabine
Montaut.
Biotransformation
of the
Cruciferous
Phytoalexin
Precursor
Indole-3-Acetaldehyde
Oxime
by Fungal
Pathogens.
85th
Canadian
Society
for
Chemistry
Conference
and
Exhibition,
June
1-5th
2002,
Vancouver,
British
Columbia
(Canada).
Poster
N°951.
M.
Soledade
C. Pedras,
Sabine
Montaut,
Corwin
M. Nycholat
and
Yiming
Xu.
Chemical
Defenses
of Canola,
Brown
Mustard
and
Turnip:
Biotransformation
and
Biosynthesis.
85th
Canadian
Society
for
Chemistry
(CSC)
Conference
and
Exhibition,
June
1-5th
2002,
Vancouver,
British
Columbia
(Canada).
Presentation
N°386.
M.
Soledade
C. Pedras,
Sabine
Montaut
S.,
Yiming
Xu,
Abdul
Q. Khan
and
Ali
Loukaci.
Assembling
the
biosynthetic
puzzle
of crucifer
metabolites:
incorporation
of indole-3-acetaldoxime
into
phytoalexins.
37th
National
Organic
Chemistry
Symposium,
June
10-14th
2001,
Bozeman,
Montana
(U.S.A.).
Poster
N°199.
M.
Soledade
C. Pedras,
Corwin
M. Nycholat,
Sabine
Montaut
and
Yiming
Xu.
Elicitation
of brassica
phytoalexins
and
biotransformation
of brassinin
in brown
mustard
and
turnip
roots.
37th
National
Organic
Chemistry
Symposium,
June
10-14th
2001,
Bozeman,
Montana
(U.S.A).
Poster
N°198.
Sabine
Montaut,
Marie-Thérèse
Fauvel,
Renato
Iori,
Patrick
Rollin,
Gérard
Vilarem
and
Isabelle
Fourasté.
Isolation
and
identification
of phenolic
compounds
and
glucosinolates
from
woad
fruits
(Isatis
tinctoria
L.).
2000
years
of natural
products
research
- Past,
present
and
future,
July
26-30th
1999,
Amsterdam
(Netherlands).
Poster
N°207.
Affiliations
•
Canadian
Society
for
Chemistry
•
Société
Française
de Chimie
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