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<title>M.Sc. Biotechnology</title>
<link>http://hdl.handle.net/10464/3047</link>
<description/>
<pubDate>Tue, 21 May 2013 16:51:27 GMT</pubDate>
<dc:date>2013-05-21T16:51:27Z</dc:date>
<item>
<title>Synthesis and utilization of guanidine catalysts for applications directed towards the preparation of butenolide and modified amino acid derivatives</title>
<link>http://hdl.handle.net/10464/4024</link>
<description>Synthesis and utilization of guanidine catalysts for applications directed towards the preparation of butenolide and modified amino acid derivatives
Lupa, Peter
Development of guanidine catalysts is explored through direct iminium chloride and&#13;
amine coupling, alongside a 2-chloro-l,3-dimethyl-IH-imidazol-:-3-ium chloride (DMC)&#13;
induced thiourea cyclization. Synthesized achiral catalyst N-(5Hdibenzo[&#13;
d,t][1,3]diazepin-6(7H)-ylidene)-3,5-bis(trifluoromethyl) aniline proved&#13;
unsuccessful towards O-acyl migrations, however successfully catalyzed the vinylogous&#13;
aldol reaction between dicbloro furanone and benzaldehyde. Incorporating chirality into&#13;
the guanidine catalyst utilizing a (R)-phenylalaninol auxiliary, generating (R)-2-((5Hdibenzo[&#13;
d,t] [1,3 ]diazepin-6(7H)-ylidene ) amino )-3 -phenylpropan-l-ol, demonstrated&#13;
enantioselectivity for a variety of adducts. Highest enantiomeric excess (ee) was afforded&#13;
between dibromofuranone and p-chlorobenzaldehyde, affording the syn conformation in&#13;
96% ee and the anti in 54% ee, with an overall yield of30%. Attempts to increase&#13;
asymmetric induction were focused on incorporation of axial chirality to the (R)phenylalaninol&#13;
catalyst using binaphthyl diamine. Incorporation of (S)-binaphthyl&#13;
exhibited destructive selectivity, whereas incorporation of (R)-binaphthyl demonstrated&#13;
no effects on enantioselectivity. Current studies are being directed towards identifying the&#13;
catalytic properties of asymmetric induction with further studies are being aimed towards&#13;
increasing enantioselectivity by increasing backbone steric bulk.
</description>
<pubDate>Wed, 04 Jul 2012 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10464/4024</guid>
<dc:date>2012-07-04T00:00:00Z</dc:date>
</item>
<item>
<title>Study of new yeast strains as novel starter cultures for Riesling icewine production</title>
<link>http://hdl.handle.net/10464/3423</link>
<description>Study of new yeast strains as novel starter cultures for Riesling icewine production
Yang, Fei
Icewine  is  a  sweet  dessert  wine  fermented  from  the  juice  of  grapes  naturally &#13;
frozen  on  the  vine.  The  production  of   Icewine  faces  many  challenges  such  as &#13;
sluggish  fermentation,  which  often  yields  wines  with  low  ethanol,  and  an &#13;
accumulation  of  high concentration  of  volatile  acidity,  mainly in the  form  of  acetic &#13;
acid.  This  project  investigated three  new  yeast  strains  as  novel  starter  cultures  for &#13;
Icewine  fermentation with particular emphasis on  reducing acetic acid production:  a &#13;
naturally occurring strain of  S.  bayanus/S.  pastorianus isolated from  Icewine grapes, &#13;
and two hybrids between S.  cerevisiae and S.  bayanus, AWRI  1571  and AWRI  1572. &#13;
These  strains  were  evaluated  for  sugar  consumption  patterns  and  metabolic &#13;
production  of   ethanol,  glycerol  and  acetic  acid,  and  were  compared  to  the &#13;
performance of a  standard commercial wine yeast KI-VI116.  The ITS  rONA region &#13;
of  the  two  A WRI  crosses  was  also  analyzed  during  fermentations  to  assess  their &#13;
genomic  stability.  Icewine  fermentations  were  performed  in  sterile  filtered juice,  in &#13;
the  absence of  indigenous microflora, and also in  unfiltered juice in  order to mirror &#13;
commercial wine making practices. &#13;
The  hybrid A WRI  1572 was  found to  be  a  promising candidate as a  novel  starter &#13;
culture for  Icewine production. I t  produced  10.3 % v/v  of  ethanol in sterile Riesling &#13;
Icewine  fermentations  and  11.2  %  v/v  in  the  unfiltered  ones  within  a  reasonable &#13;
fermentation time (39 days).  Its acetic acid production per gram sugar consumed was &#13;
approximately  30%  lower  in  comparison  with  commercial  wine  yeast  K I -V 1116 &#13;
under  both  sterile  filtered  and  unfiltered  fermentations.  The  natural  isolate  S. bayanus/S. pastorianus and AWRI  1571  did not appear to be suitable for commercial &#13;
Icewine production.  They reached the target ethanol concentration of  approximately &#13;
10 % v/v in 39 day fermentations and also produced less acetic acid as a function of  &#13;
both  time  and  sugar  consumed  in  sterile  fermentations  compared  to  KI-V1116. &#13;
However,  in  unfiltered  fermentations,  both  of  them  failed  to  produce  the  target &#13;
concentration  of  ethanol  and  accumulated  high  concentration  of  acetic  acid.  Both &#13;
A WRI  crosses displayed higher loss  of  or  reduced copies in  ITS  rDNA region  from &#13;
the S.  bayanus parent compared to the S.  cerevisiae parent;  however, these  genomic &#13;
losses could not be  related to the metabolic profile.
</description>
<pubDate>Fri, 14 Oct 2011 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10464/3423</guid>
<dc:date>2011-10-14T00:00:00Z</dc:date>
</item>
<item>
<title>The structure of arabidopsis NPR1 : its function as a salicylic acid receptor and a metal-binding protein</title>
<link>http://hdl.handle.net/10464/3422</link>
<description>The structure of arabidopsis NPR1 : its function as a salicylic acid receptor and a metal-binding protein
Zhang, Di
The  Arabidopsis NPRI  protein  regulates  systemic  acquired  resistance  dependent  on &#13;
salicylic acid.  Analyses by plant two-hybrid analysis in  vivo  and  pull-down assays in &#13;
vitro  showed  that  the  BTB/POZ  domain  of  NPRI  at  the  N-terminus  serves  as  an &#13;
autoinhibitory  domain  to  negate  the  function  of  the  transactivation  domain  at  the &#13;
C-terminus through  direct  binding  of  these two  domains.  I t  was  also  shown  that the &#13;
binding  of  the  BTB/POZ  domain  to  the  C-terminus  of  NPRI  was  abolished  by  SA &#13;
treatment,  suggesting  that  SA  could  interfere  directly  with  this  binding.  By  gel &#13;
filtration,  it  was  demonstrated that  SA affects the  conformation  of  full-length  NPRl ,  &#13;
confirming the  role  of  NPRI  as  an  SA  receptor.  Gel  filtration  analysis also  indicated &#13;
that  NPRI  could  be  converted  from  an  oligomer  to  a  dimer  with  SA  treatment. &#13;
Furthermore,  one N-terminal deletion ~513 has been  shown to act as a metal-binding &#13;
protein  and  its  two  Cys-521  and  Cys-529  are  important  for  binding  to  Ni&#13;
2&#13;
+  by &#13;
pull-down assays.
</description>
<pubDate>Fri, 14 Oct 2011 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10464/3422</guid>
<dc:date>2011-10-14T00:00:00Z</dc:date>
</item>
<item>
<title>Elucidation of the components involved in the antioxidant activity of honey</title>
<link>http://hdl.handle.net/10464/3416</link>
<description>Elucidation of the components involved in the antioxidant activity of honey
Miotto, Danielle
Canadian honeys were analyzed for sugar concentration, honey colour, total &#13;
phenolic content, the level of  brown pigments, and antioxidant activity in order to &#13;
elucidate the main components involved in the antioxidant activity of  honey. By &#13;
employing size-exclusion chromatography in combination with activity-guided &#13;
fractionation, it was demonstrated that the antioxidant components are of  high molecular &#13;
weight (HMW), brown in colour and absorb at both 280nm and 450nm. The presence of  &#13;
brown HMW antioxidant components prompted an investigation on the influence of  heattreatment on the Maillard reaction and the formation of  melanoid ins. Heat-treatment of  &#13;
honey resulted in an increase in the level of  phenolics in the melanoidin fractions which &#13;
correlated with an increase in antioxidant activity. The preliminary results of  this study &#13;
suggest for the first time that honey melanoidins underlie the antioxidant activity of  &#13;
unheated and heat-treated honey, and that phenolic constituents are involved in the &#13;
melanoidin structure and are likely incorporated by covalent or non-covalent interaction.
</description>
<pubDate>Fri, 14 Oct 2011 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10464/3416</guid>
<dc:date>2011-10-14T00:00:00Z</dc:date>
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