Efectul de prelucrare c-âldur-â pe detectarea PCR a modificate genetic (MG), soia +«n produsele...
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Transcript of Efectul de prelucrare c-âldur-â pe detectarea PCR a modificate genetic (MG), soia +«n produsele...
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New Biotechnology Volume 29S September 2012
Keywords:Antibacterial; Lactic acid bacteria; Escherichia coli;
Lactobacillus delbrueckii
http://dx.doi.org/10.1016/j.nbt.2012.08.352
Poster 3.2.18
Influence of boron toxicity on global expression profiles
in wheat (Triticum aestivumL.)
C. Kayihan 1,, M.T. Oz 1, F. Eyidogan 2, M. Yucel 1, H.A. Oktem 1
1Middle East Technical University, Department of Biology, 06800
Ankara, Turkey2Baskent University, Faculty of Education, 06810, Ankara, Turkey
Excess boron (B) is known to negatively affect plant growth.
However, the molecular mechanism of toxicity in plants is not sat-
isfactory elucidated. In this study, global expression differences in
wheat (Triticum aestivumL. cv. Atay-85 and Bolal-2973) leaves and
roots under B toxicity were investigated using DNA microarrays.
Eight day old aseptically grown seedlings were subjected to 5 mM
H3BO3 for 5 days. Total RNAs from leaf or root tissues were isolated
and checked by Bioanalyzer 2100. Expression profiles were deter-mined with Wheat GeneChip. Among 61127 transcripts each
represented with a probe set on the GeneChip fold change of at
least 2 andpvalue of at most 0.05 was considered as an indication
of significant alteration in expression. Compared to unstressed
control (10M H3BO3) conditions, B toxicity resulted in signif-
icant regulation of more than 1000 transcripts in leaf and root
tissues of both cultivars. Furthermore,the numbers of genes signif-
icantly expressed in Atay-85 were higher than those in Bolal-2973.
Transcripts altered under B toxicity included genes coding for tran-
scription factors, peroxidases, ribosomal proteins, and hydrolases
and functioning in biosynthesis of phenylpropanoids. Responsive
genes determined in this study will provide insight into succes-
sive studies on molecular mechanism of tolerance to B toxicity inwheat.
http://dx.doi.org/10.1016/j.nbt.2012.08.353
Poster 3.2.19
Amorfrutins are efficient natural antidiabetics
Christopher Weidner, David Meierhofer, Sascha Sauer
Otto Warburg Laboratory, Max Planck Institute for Molecular Genetics,
Ihnestrae 63-73, 14195 Berlin, Germany
Worldwide increases in the incidence of metabolic diseases call for
alternative strategies for preventing and treating these disorders.
Compounds from edible natural resources provide a structurally
diverse resource to alleviate complex diseases by nutritional inter-
vention. We discovered a family of natural antidiabetics, the
amorfrutins, isolated from two legumes, Glycyrrhiza foetida and
Amorpha fruticosa [1]. The amorfrutins selectively activate the
nuclear receptor PPAR, which results in gene expression andphys-
iological profiles markedly different from activation by known
synthetic PPAR ligands. In metabolic mouse models, amor-
frutins strongly increased insulin sensitivity and improved other
physiological parameters. Using proteome-wide quantitative mass
spectrometry we monitored the treatment of diet-induced obese
mice with the amorfrutins and the diabetes drug rosiglitazone in
adipose tissue, liver and the heart. In contrast to microarray-based
gene expression analysis, we detected striking indication for the
unwanted molecular events of rosiglitazone leading to heartfailure
and other known side effects. The methodology introduced here
can be used for systematic proteome-wide screenings of drug can-
didates and can be adapted further to human patient biopsies. Insummary, we showed that application of diet-derived compounds
may constitute a promisingstrategy to combatcommon metabolic
diseases.
Reference
1. Weidner C, et al.Proc Natl Acad Sci USA 2012;109(May (19)):725762.
http://dx.doi.org/10.1016/j.nbt.2012.08.354
Poster 3.2.20
Liposomes and liposomal nanoemulsions from sunflower
S. Shulga , I. Glukh
Institute for Food Biotechnology and Genomics, National Academy of
Science of Ukraine 2, Osypovskogo str., 04123, Kyiv-123, Ukraine
Sunflower lecithin gives manufactures an attractive alternative
to soy lecithin, without requiring allergen labeling. Sunflower
lecithin is an ideal solution forproducing chocolate, chewing gum,
sauces or instantized foods offering smoothness, fine texture and
good emulsifying properties and drug delivery systems. Use of the
sunflower phosphatide concentrate as source material is one of
promising trends for the commercial use of phosphatidylcholine.
Liposomal technology is readily applied in medicine, cosme-
tology and pharmacology. The experience of encapsulation ofbioactive substances can be useful in food technology.
In the study liposomes were prepared from sunflower lecithin
by some methods. The structure of liposomes and particle size
were analyzed and compared. The possibility of using empty
liposomes as transporting nanosystems was studied. Technology
parameters and conditions for their stability and long-term storage
were investigated as well.
Keywords:Lecithin; Sunflower; Liposomes
http://dx.doi.org/10.1016/j.nbt.2012.08.355
Poster 3.2.21
The effect of heat processing on PCR detection of Genet-ically Modified (GM) soya in meat products
zge zgen Arun, Karlo Muratoglu, Funda Yilmaz
Istanbul University, Veterinary Faculty Food Hygiene, Technology
Department, Turkey
The plantation of GMOs are growing rapidly since they were first
commercialized in 1996. Significant ratio of globally planted soya
is GM. However the public concern over GMOs is growing as
rapidly. Thus most countries and finally Turkish Republic have
released regulations on labeling of GMOs. For this purpose devel-
www.elsevier.com/locate/nbt S127
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8/10/2019 Efectul de prelucrare c-ldur- pe detectarea PCR a modificate genetic (MG), soia +n produsele din carne
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New Biotechnology Volume 29S September 2012
oping sensitive methods for detection of GMOs is necessary. PCRis
the most common method used thus far. However processing fac-
tors (low pH,heat, etc.) effects the DNAquality and PCR detection.
Addition of soya to the meat products is common in many coun-
tries and most of them have low pH and heated. The aim of this
study was to evaluate combine effect of heat and pH on PCR detec-
tion of GM soya. Sausage mixtures containing various amounts of
GM soya were prepared, and process simulations were performedrepresenting common pH values and heating temperatures used
for meat products. The effect of heat was inspected by detection
of CaMV 35 S which is a novel sequence present in most GMOs
and lectin which is present in both GM and non GM soya. The
results proved that low amounts of GM soya can still be detected
in processed meat products although low pH and temperature has
an effect on detection limit.
Keywords:GMO; PCR; Soya; DNA
http://dx.doi.org/10.1016/j.nbt.2012.08.356
Poster 3.2.22
Heterologous expression of a barley boron transportergene in tobacco (Nicotiana tabaccum) and analysis of
transgenic plants
Doga Gmsel 1,, M. Tufan Oz 2, Fsun Eyidogan3, Meral Ycel 2,
Yelda zden Ciftci 1, Hseyin Avni ktem 2
1 Gebze Institute of Technology, Department of Molecular Biology,
41400 Kocaeli, Turkey2Middle East Technical University, Department of Biological Sciences,
06800 Ankara, Turkey3Baskent University, Faculty of Education, 06810, Ankara, Turkey
High concentration of boron (B) in soil decreases agricultural yield
in arid and semi-arid regions throughout the world. A proposed
strategy to confer tolerance to B stresses in crops is stable transfor-mation of target plants with genes encoding B tolerance proteins
such as efflux/influx transporters. Therefore in this study, barley B
transporter gene HvBor1awas transferred to the model organism
tobacco via Agrobacterium-mediated transformation to improve
tolerance to B toxicity. Plant transformation vectors pIPKb004
containingHvBor1aand pEarleyGate100 containingHvBor1a-GFP
fusion were transferred to A. tumefaciensstrain C58C1 using elec-
troporation. Leaf disc transformation of tobacco (cv. Samsun and
Petit Havana) and indirect organogenesis were utilized to generate
putative transgenics constitutively expressing HvBor1a. The inte-
gration and expression of gene of interest was confirmed with
molecular analysis. Additionally, B toxicity bioassays were per-
formed to examine the altered phenotype of transgenics and firstgeneration of plants. In conclusion, results of this study suggested
that theHvBor1agene might be of great value in engineering tol-
erance to B toxicity in crop plants.
http://dx.doi.org/10.1016/j.nbt.2012.08.357
Poster 3.2.23
Continuous nisin production ofLactococcus lactisimmo-
bilized with surface displayed chitin binding domain on
chitin
Burcu Krdikanlioglu, mer Simsek
University of Pamukkale, Department of Food Engineering, Denizli,
Turkey
In this study, nisin production ofLactococcus lactisstrains express-
ing surface displayed chitin binding domain (ChBD) wereanalyzed
in a chitin containing continuous fermentation system. In this
respect, two ChBD-displayedL. lactisstrains (PLAC2 and PLAC7),
previously constructed with fusing the chitin binding domain to
C-terminal part(344 or 800 amino acid) of the PrtPofL. lactis, were
used separately. These ChBD-displayed strains were immobilized
to chitin and subsequently included in a continuous fermentation
system with 0.10.9 dilution rates. Nisin production and biomass
concentration dramatically reduced for control strains at high
dilution rates where high nisin and biomass production was main-
tained at both ChBD-displayed L. lactis strains. Maximum nisinproduction at control strains used in a fermentation system with
or without chitin was determined as 2120 IU ml1 where ChBD-
displayedstrains with 344aa or 800aa C-terminal of prtP produced
4920IUml1 and 5520IU ml1 nisin respectively. Besides, nisin
productivityof control strains with or without chitinexistence was
measured as 812IUml1 h and 636IUml1 h respectively. How-
ever, this was measured as 2709IU ml1 h withL. lactisPLAC2 and
4581IUml1 h withL. lactisPLAC7 meaning that nisin productiv-
ity of cells could be improved 7-fold higher. We concluded that
800 aa long C-terminal part of PrtP is more functional and yielded
higher productivity. Also surface displayed chitin binding domain
at nisin producerL. lactiscould be used efficiently in continuous
fermentation system.
Keywords:Lactococcus lactis; Nisin; Chitin binding domain;
Continuous fermentation
http://dx.doi.org/10.1016/j.nbt.2012.08.358
Poster 3.2.24
Production of monoclonal antibody against Staphylo-
coccal Enterotoxin A (SEA)
Arzu Pnarbas 1,, Elif Yolac 1, zlem Ertekin 2, Fatma Ycel 2
1Kocaeli University, Faculty of Medicine, Department of Medical Genet-
ics and Molecular Biology, Umuttepe, Kocaeli, Turkey2 TUBITAK, MAM, Institute for Genetic Engineering and Biotechnology,
Gebze, Kocaeli, Turkey
Staphylococcal Enterotoxins (SEA) cause syndromes like toxic
shock, arthritis, allergic reactions and autoimmune diseases beside
food poisoning. The mortality rate is low for staphylococcal food
poisoning but for children and elderly the mortality rate is in the
range of 0.034.4%. Staphylococcal poisonings causes economical
burden due to loss in the production and medical costs.
SEA is the most common toxic, heat and acid-resistant toxin
among all the SEAs. SEA causes serious contamination around the
S128 www.elsevier.com/locate/nbt