P001-98 Chilling
induced chnges in membrane fluidity and antioxidant enzyme
activities in Coffea arabica roots
Queiroz CGS,
Alonso A, Mares-Guia M, Magalhães AC*
Biologia Plantarum
41: 403-413, 1998
*Fone: 788-7696; 788-7032
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P003-98 Tobacco
mosaic virus disasembly by high hydrostatic pressure in combination
with urea and low temperature
Bonafe CFS,
Vital CMR, Telles RCB, Gonçalves MC, Matsuura MSA, Pessine
FBT, Freitas DRC, Vega J*
The effect of
low temperature and urea combined with high pressure was studied
on tobacco mosaic virus (TMV). The evaluation of its aggregation
state and denaturation process was studied using gel filtration,
transmission, electron microscopy, and spectroscopic methods.
The incubation at 2.5 kbar induced 18% dissociation, and decreasing
of temperature to -19 °C promoted additional dissociation
to 72%, with stabilization of the dissociation products. Under
such conditions , extensive denaturation did not occur. The
apparent enthalpy and entropy of dissociation indicated that
the TMV association is an entropicly driven process. The apparent
free energy of stabilization given by the presence of RNA
is at least -1.7 kcal/mol subunit. Urea-induced dissociation
of TMV samples and incubation at high-pressure promoted a
higher degree of dissociation. High-pressure induced remarkable
TMV denaturation in the presence of 2.5 M urea, with a volume
change of -101 mL/mol of denatured subunit. The apparent enthalpy
and entropy of denaturation by 1.75 M urea at 2.5 kbar was
-11.1 and -10.2 kcal/mol subunit, respectively, demonstrating
that the TMV protein coat presents an apparent free energy
of denaturation by urea close to zero. These thermodynamic
parameters could be derived by assuming a steady-state condition.
Biochemistry 37: 11097-11105, 1998
*E-mail: jvega@turing.unicamp.br
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P004-98 Indole-3-acetic
acid biosynthesis by bacteria Xanthomonas axonopodis cv citri
is increased in the presence of leaf extracts
Costacurta
A, Mazzafera P*, Rosato YB
Indole-3-acetic
acid production by Xanthomonas strains pathogenic to
citrus was analyzed by reversed-phase high-performance liquid
chromatography, thin-layer chromatography, UV spectroscopy
and gas chromatography-mass spectrometry, and quantified by
high-performance liquid chromatography with fluorescence detection.
Amounts of auxin produced by Xanthomonas strains were
low when compared with indole-3-acetic acid biosynthesis by
other bacteria. In three different experiments it was shown
that the addition of plant leaf extracts to bacterial cultures
increased indole-3-acetic acid biosynthesis by Xanthomonas
axonopodis pv. citri 223. Microbiology Letters 159:
215-220, 1998
*E-mail: pmazza@obelix.unicamp.br
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P005-98 Oil
content of green beans from some coffee species
Mazzafera
P*, Soave D, Zullo MAT, Guerreiro Filho O
The oil content
was determinei in seeds of several continental African species
of the coffee germplasm bank of Instituto Agronômico de Campinas,
State of São Paulo, Brazil. Oil was extracted from seeds with
hexane in Soxhlet apparatus. Due to the economic importance,
C. arabica and C. canephora have been the best studied
species concerning oil content and composition, and the results
obtained are in agreement with the reported in the literature.
On the other hand, only one report in the literature describes
the results of oil analyses in other few species of the African
continent, aithough it does not allow comparison with our
results. The oil content of most of the species varied from
9 to 15%, therefore, similar to the range observed for C.
arabica and C. canephora. The exception was C. salvatrix,
with 29% of oil in the seeds. Bragantia 57: 45-48,
1998
*E-mail: pmazza@obelix.unicamp.br
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P006-98 Growth
and biochemical alterations in coffee due to selenite toxicity
Mazzafera
P*
Two experiments
were conducted to investigate selenite toxicity in coffee
(Coffea arabica cv. Catuaí). In the first aqueous selenite
solution (10 gM Na2SeO3) was used to infiltrate leaves of
an adult coffee plant. The infiltrated leaves and fruits adjacent
to them showed enhanced contents of caffeine and soluble sugars.
Amino acid contents were not affected, whereas pigments (chlorophylls,
carotenoids and xanthophylls) exhibited a significant decrease.
In the second experiment, coffee seedlings were irrigated
with aqueous selenite solutions (10,100 and 1000 JIM
Na2SC03) and the first and third pairs of leaves were analyzed.
Control plants did not receive selenium. The plants were not
different in height, but at the highest selenium concentration
showed lower dry matter accumulation in roots and leaves,
lower leaf area and thicker leaves. Increases in caffeine
and soluble sugars were observed in the first pair of leaves
at the highest selenium concentration, although selenium content
itself increased steadily with increasing solution concentration.
Phenols increased in both leaf pairs and pigments decreased
in the third pair. Nitrate reductase activity, measured in
the second leaf pair, was much lower at all selenium levels.
The profile of free amino acid was altered in leaves of plants
treated with selenium.
Plant and Soil 201: 189-196, 1998
*E-mail: pmazza@obelix.unicamp.br
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P071-98 Differential
expression of a novel gene in response to coronatine, methyl
jasmonate, and wounding in the coil mutant of Arabidopsis
Benedetti
CE, Costa CL, Turcinelli SR, Arruda P*
Coronatine is
a phototoxin produced by some plant-pathogenic bacteria. It
has been shown that coronatine mimics the action of methyl
jasmonate (MeJA) in plants. MeJA is a plant-signaling molecule
involved in stress responses such as wounding and pathogen
attack. In Arabidopsis thaliana, MeJA is essential
for pollen grain development. The coil (for coronatine-insensitive)
mutant of Arabidopsis produces sterile male flowers
and shows an altered response to wounding. When the differential
display technique was used, a message was rapidly induced
by coronatine in wild-type plants but not in coil. The corresponding
cDNA was cloned. The coronatine-induced gene ATHCOR1 (for
A. thaliana coronatine-induced) is expressed in seedlings,
mature leaves, flowers, and siliques but was not detected
in roots. The expression of this gene was dramatically reduced
in coil plants, indicating that COI1 affects its expression.
ATHCORRR1 was rapidly induced by MeJA and wounding in in wild-type
plants. The sequence of ATHCOR1 shows no strong homology to
known proteins. However, the predicted polypeptide contains
a conserved amino acid sequence present in several bacterial,
animal and plant hydrolases and includes a potential ATP/GTP-binding-site
motif (P-loop).
Plant Physiology 116: 1037-1042, 1998
*E-mail: parruda@turing.unicamp.br
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P072-98 The
molecular and functional characterization of an Opaque2 homologue
gene from Coix and a new classification of plant bZIP proteins
Vettore AL,
Yunes JA, Neto GC, da Silva MJ, Arruda P*, Leite A
The seed storage
proteins of Coix, sorghum and maize are codified by homologous
genes which are coordinately expressed in the endosperm in
a temporal-specific fashion. Opaque2 (O2), a bZIP protein
originally isolated from maize, has been described as a transcription
activator of alpha- and beta-prolamin genes. The isolation
and characterization of cDNA and genomic clones encoding the
Opaque2 homologue from Coh are reported here. The coding region
of the Coix O2 gene is interrupted by five introns and codifies
a polypeptide of 408 amino acids. Comparison of the deduced
amino acid sequence with two different sequences of maize
O2 protein showed that the Coix O2 protein is similar to the
maize O2 isolated from W22 maize inbred line. The Coix O2
protein has the same binding specificity and expression pattern
of the maize O2. The O2 proteins together with OHP1, OsBZIPPA,
SPA, CPRF2 and RITA1 were assigned to one of the five bZIP
plant families in an updated classification of plant bZIP
according to bZIP domain similarity. Plant Molecular Biology
36: 249-263, 1998
*E-mail: parruda@turing.unicamp.br
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P073-98 Cooperative
DNA binding and sequence discrimination by the Opaque2 bZIP
factor
Yunes JA,
Vettore AL, Silva MJ, Leite A, Arruda P*
The maize Opaque2
O2) protein is a basic leucine zipper transcription factor
that controls the expression of distinct classes of endosperm
genes through the recognition of different cis-acting elements
in their promoters. The O2 target region in the promoter of
the coixin gene was analyzed in detail and shown to
comprise two closely adjacent binding sites, named O2u and
O2d, which are related in sequence to the GCN4 binding site.
Quantitative Dnase footprint analysis indicated that O2 binding
to coixin target sites is best described by a cooperative
model. Transient expression assays showed that the two adjacent
sites act synergistically. This synergy is mediated in part
by cooperative DNA binding. In tobacco protoplasts, O2 binding
at the O2u site is more important for enhancer activity than
is binding at the O2d site, suggesting that the architecture
of the O2-DNA complex is important for interaction with the
transcriptional machinery.
Plant Cell 10: 1941-1956, 1998
*E-mail: parruda@turing.unicamp.br
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CD-ROM, LIVROS,
CAPÍTULOS DE LIVROS
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C001-98
N2 fixation in Crotalaria juncea L.:
effect of NO3 and NH4
Mendonça E,
Schiavinato M*
In Proceedings
of 16th World Congress of Soil Science, 20 - 26/08/1998,
Montpellier, FRANÇA, trabalho completo em CDROM
*E-mail: mschiavi@obelix.unicamp.br
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TRABALHOS ACEITOS
EM PERIÓDICOS
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A062-98 = A067-98
E-mail: anete@turing.unicamp.br
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