Team:NTU Taiwan/index.html
From 2013.igem.org
(Difference between revisions)
Ddmail2009 (Talk | contribs) |
Ddmail2009 (Talk | contribs) |
||
Line 138: | Line 138: | ||
<div class="col-md-3"> | <div class="col-md-3"> | ||
<a href="https://2013.igem.org/Main_Page" class="brand"> | <a href="https://2013.igem.org/Main_Page" class="brand"> | ||
- | <img src=" | + | <img src="https://static.igem.org/mediawiki/2011/a/a9/DTU-Denmark2011-IGEM_logo.png" alt=""> |
</a> | </a> | ||
- | < | + | <div>2013 © NTU-Taiwan.</div> |
- | < | + | <div class="divide">Please contact us<br/> If we violate any copywright</div> |
- | < | + | <div>Produced by <br> <a href="mailto:b99902006@ntu.edu.tw" target="_blank">PoHsien Wang</a></div><br> |
</div> | </div> | ||
<div class="col-md-6 thanks"> | <div class="col-md-6 thanks"> | ||
<h2> Special Thanks</h2> | <h2> Special Thanks</h2> | ||
- | <img src="images/thanks/BST.png" alt=""> | + | <img src="https://static.igem.org/mediawiki/2013/5/5f/BST.png" alt-src="images/thanks/BST.png" alt=""> |
- | <img src="images/thanks/CSIE.png" alt=""> | + | <img src="https://static.igem.org/mediawiki/2013/2/29/CSIE.png" alt-src="images/thanks/CSIE.png" alt=""> |
- | <img src="images/thanks/NTHU.png" alt=""> | + | <img src="https://static.igem.org/mediawiki/2013/d/d6/NTHU.png" alt-src="images/thanks/NTHU.png" alt=""> |
- | <img src="images/thanks/NTU.png" alt=""> | + | <img src="https://static.igem.org/mediawiki/2013/c/c1/NTU.png" alt-src="images/thanks/NTU.png" alt=""> |
- | <img src="images/thanks/ntuee.png" alt=""> | + | <img src="https://static.igem.org/mediawiki/2013/c/c2/Ntuee.png" alt-src="images/thanks/ntuee.png" alt=""> |
</div> | </div> | ||
<div class="col-md-3"> | <div class="col-md-3"> | ||
Line 250: | Line 250: | ||
</section> | </section> | ||
<div class="container divide"> | <div class="container divide"> | ||
- | <p | + | <p class="col-md-8"> |
- | + | In Taiwan, fish farmers lose a large amount of fish, because temperature falls dramatically when cold current comes in winter. Ofcourse, fish farmers try to prevent fish from death dying; however, the current methods do not work well. Moreover, they cause damage to the environment. In 2013 iGEM competition, NTU-Taiwan team tries to make a bio-heating device. We transform the SrUCP (uncoupling protein) into yeast. UCP is thermogenic protein which can produce heat by interacting with the electron transport chain. By designing the gene circuit, we want to well control the power of the bio-heating device. In addition, we want to simulate the pound environment in reality by computer and the test results after using our device in low temperature. | |
- | + | </p> | |
- | </p> | + | <div class="col-md-4"> |
+ | <img class="img-responsive" src="https://static.igem.org/mediawiki/2013/8/8f/NTU_TAIWAN_Temp.jpg" alt-src="images/temp.jpg"> | ||
+ | </div> | ||
</div> | </div> | ||
</div> | </div> | ||
Line 292: | Line 294: | ||
</div> | </div> | ||
<p> | <p> | ||
- | Mitochondria uncoupling proteins 1(UCP1) are members of the family of mitochondrial anion carrier proteins (MACP). It facilitates the transfer of anions from the inner to the outer mitochondrial membrane and the return transfer of protons from the outer to the inner mitochondrial membrane. UCPs separate oxidative phosphorylation from ATP synthesis with energy dissipated as heat, also referred to as the mitochondrial proton leak. | + | Mitochondria uncoupling proteins 1(UCP1) are members of the family of mitochondrial anion carrier proteins (MACP). It facilitates the transfer of anions from the inner to the outer mitochondrial membrane and the return transfer of protons from the outer to the inner mitochondrial membrane. [2][3]UCPs separate oxidative phosphorylation from ATP synthesis with energy dissipated as heat, also referred to as the mitochondrial proton leak. |
</p><p> | </p><p> | ||
- | + | UCP has been found in several species, including mammals and plants. Skunk cabbage(Symplocarpus foetidus)is a thermogenic plant, using srUCPs to resist in dramatic temperature decreases in the environment. In 1999, Dr. Kikukatsu Ito found that there are two types of SrUCPs, designated as SrUCPA and SrUCPB [4]. SrUCPA is proposed to be the functional thermogenic prtein, and SrUCPB serves as a regulator in thermogenesis in Skunk cabbage.[5][6] We use SrUCPA gene as our material to construct our plasmid. | |
+ | [1] Brown adipose tissue: function and physiological significance. Cannon B, Nedergaard J. Physiol Rev. 2004 Jan. | ||
+ | [2] Uncoupling proteins: the issues from a biochemist point of view. Klingenberg M, Echtay KS. Biochim Biophys Acta. 2001 Mar 1;1504(1):128-43. | ||
+ | [3] Mitochondrial Uncoupling Proteins in Mammals and Plants. Jirı´ Borecky´, Ivan G. Maia, and Paulo Arruda. Bioscience Reports, Vol. 21, No. 2, April 2001 (2001). | ||
+ | [4] Isolation of two distinct cold-inducible cDNAs encoding plant uncoupling proteins from the spadix of skunk cabbage (Symplocarpus foetidus). Kikukatsu Ito. Plant Science Vol. 149, Issue 2, 3 Dec. 1999, P.167–173. | ||
+ | [5] Characterization of the plant uncoupling protein, SrUCPA, expressed in spadix mitochondria of the thermogenic skunk cabbage. Yasuko Ito-Inaba, Yamato Hida, Megumi Ichikawa, Yoshiaki Kato and Tetsuro Yamashita. Journal of Experimental Botany, Vol. 59, No. 4, pp. 995–1005, 2008. | ||
+ | [6] Functional Coexpression of the Mitochondrial Alternative Oxidase and Uncoupling Protein Underlies Thermoregulation in the Thermogenic Florets of Skunk Cabbage. Yoshihiko Onda, Yoshiaki Kato, Yukie Abe, Takanori Ito, Miyuki Morohashi, Yuka Ito,Megumi Ichikawa4, Kazushige Matsukawa, Yusuke Kakizaki, Hiroyuki Koiwa, and Kikukatsu Ito. Plant Physiology, February 2008, Vol. 146, pp. 636–645. | ||
+ | |||
</p> | </p> | ||
</div> | </div> | ||
Line 345: | Line 354: | ||
</section> | </section> | ||
<div class="row" style="margin-left: 20px; margin-right: 20px"> | <div class="row" style="margin-left: 20px; margin-right: 20px"> | ||
- | + | <img class="pull-right img-responsive" src="./images/UT_conference.jpg"> | |
- | + | <div class="row text-center" style="margin-top: 90px"> | |
- | + | <b><h2>Conference with UT_Tokyo Team</h2></b><br/> | |
- | + | On 4th May, We held a video conference with UT_Tokyo team. It's our first time to have video conference with foreign iGEM team! We gave a briefly project introduction and discussed about experimental problems to each other. By the discussion, we found out some bugs but some new ideas in our project. On the other hand, we also gave some advices to UT_Tokyo team. That's a great chance for us to practice how can we express our project entirely and clearly. | |
+ | </div> | ||
</div> | </div> | ||
<div class="row" style="margin-left: 20px; margin-right: 20px"> | <div class="row" style="margin-left: 20px; margin-right: 20px"> | ||
- | + | <img class="pull-left img-responsive" src="./images/UT_conference in Tokyo.jpg"> | |
- | + | <div class="row text-center" style="margin-top: 150px"> | |
- | + | <b><h2>Conference in Tokyo University</h2></b><br/> | |
- | + | On 14th July, Yi-Yuan Lee met UT_Tokyo iGEM team in Tokyo University. UT_Tokyo team briefly performed their currently progress and started to discuss their project. For Yi-Yuan, he learned more experience about how to well organitze an iGEM team. | |
- | + | </div> | |
</div> | </div> | ||
<div class="row" style="margin-left: 20px; margin-right: 20px"> | <div class="row" style="margin-left: 20px; margin-right: 20px"> | ||
- | + | <img class="pull-right img-responsive" src="./images/Purdue_conference.jpg"> | |
- | + | <div class="row text-center" style="margin-top: 150px"> | |
- | + | <b><h2>Conference with Purdue iGEM Team</h2></b><br/> | |
- | + | We had a video conference with Purdue iGEM team, Manchester iGEM team, TU Eindhoven iGEM team, and Kyoto iGEM team on July 8th. This is Purdue iGEM team’s project. They want to build up a new standardized form for BioBricks register by cooperating and discussing with worldwide iGEM teams. We complete the questionnaire and gave them some advices. | |
+ | </div> | ||
</div> | </div> | ||
+ | |||
+ | <div class="row" style="margin-left: 20px; margin-right: 20px"> | ||
+ | <img class="pull-left img-responsive" src="./images/Berkeley_conference.jpg" width=700 height=525> | ||
+ | <div class="row text-center" style="margin-top: 150px"> | ||
+ | <b><h2>Conference in UC Berkeley</h2></b><br/> | ||
+ | YI-Yuan and Chi-Wei had a face to face conference with Berkeley iGEM team on July 10th. We presented project and experimental design to each other, and discussed about better methods to break through our problems.<br/> | ||
+ | After the conference, we had a late lunch together in fornt of the UC Berkeley with Berkeley iGEMers. We talked from our major to where did we come from. That was a great meal with them. | ||
+ | </div> | ||
</div> | </div> | ||
<div class="row" style="margin-left: 20px; margin-right: 20px"> | <div class="row" style="margin-left: 20px; margin-right: 20px"> | ||
- | + | <img class="pull-right img-responsive" src="./images/Chiao_Tung_Conference/(27).jpg" width=700> | |
- | + | <div class="row text-center" style="margin-top: 100px"> | |
- | + | <b><h2>Conference in Chiao Tung University</h2></b><br/> | |
- | + | iGEM NTU_Taiwan team participated in the conference which was hold by Chiao Tung Univeristy. There were 7 teams joined this ceonference, the iGEM team from China, Hong Kong, and most of the iGEM teams in Taiwan. We followed the rule of iGEM which has 20 minute presentation and followed by Q & A time.<br/> | |
- | + | By this chance, we made friends with iGEMers from different teams and learned a lot of experience from them. After the conference, we had a short trip in Taipei. That was really a great time. | |
</div> | </div> | ||
</div> | </div> | ||
- | |||
<section class="purple-background"> | <section class="purple-background"> | ||
- | + | <h1 class="header">NTU Azalea Festival</h1> | |
</section> | </section> | ||
<div class="container divide essay"> | <div class="container divide essay"> | ||
- | + | <div class="row divide" style="margin-left: 20px; margin-right: 20px"> | |
- | + | <div class="col-md-6"> | |
- | + | <img class="pull-left img-responsive" src="./images/AZALEA/(1).jpg"> | |
- | NTU Azalea Festival is a anneal event for introducing each department to senior high school students. By this chance, we wanted to spread the iGEM idea to high school students. We design a simple | + | </div> |
+ | <div class="col-md-6"> | ||
+ | <img class="pull-right img-responsive" src="./images/AZALEA/(10).jpg"> | ||
+ | </div> | ||
+ | </div> | ||
+ | |||
+ | <p class="row text-left"> | ||
+ | NTU Azalea Festival is a anneal event for introducing each department to senior high school students. By this chance, we wanted to spread the iGEM idea to high school students. We design a simple computer game which contain the concept of synthetic biology, molecular biology and bio-Technology. First, we asked them to choose a right enzyme to digest the glactose. And in second level, we asked them to make the enzyme they used in previous level by amino acids, right RNA, and right enzyme. In the last level, we asked them to build up a operon for galactase production. | ||
+ | </p> | ||
</div> | </div> | ||
Line 391: | Line 417: | ||
</section> | </section> | ||
<div class="container divide essay"> | <div class="container divide essay"> | ||
- | + | <div class="row" style="margin-left: 20px; margin-right: 20px"> | |
- | + | <div class="col-md-4"> | |
+ | <img class="img-responsive" src="./images/MEETING/Meeting-(10).jpg" width=400> | ||
+ | </div> | ||
+ | |||
+ | <div class="col-md-8 text-left" style="margin-top: 150px"> | ||
+ | <p>Every year, graduate students have poster presentation in the college of life science. In this year, NTU_Taiwan team also participated in the poster presentation and introduced what is iGEM competition to the students in our college.<br/></p> | ||
+ | <p> | ||
+ | In the activity, we discussed with many professors in our college. Most of them though that this project is quite novel and crazy. | ||
+ | </p> | ||
+ | </div> | ||
+ | </div> | ||
</div> | </div> | ||
Line 399: | Line 435: | ||
</section> | </section> | ||
<div class="container divide essay"> | <div class="container divide essay"> | ||
- | <p> | + | <div class="row text-center" style="margin-left: 20px; margin-right: 20px"> |
+ | <h3>Let us introduce our App in this short film :)</h3><br/> | ||
+ | <iframe id="appMovie" style="width=75%;" src="http://www.youtube.com/embed/NjNNvrgOozA" frameborder="0" allowfullscreen></iframe><br/></div></div> | ||
+ | <div class="container divide essay"> | ||
+ | <p> | ||
+ | As we known, for most of people who has never learned synthetic biology, it‘s a magical and crazy idea to take biological parts as the electronic parts. Moreover, someone might be scaried about this technique just like "Witch Hunt" in middle centry, because he don‘t know what is it. | ||
+ | </p> | ||
+ | <p> | ||
+ | When we talk about synthetic biology, most of our friends will connect this technique with "Genome Modified Organism" and "Terrible Biological Weapon". They have antagonistic feeling in the first time because they don‘t know about it. However, beyond our expectation that they still feeling unbelieveble after our explaination...... | ||
+ | </p> | ||
+ | <p> | ||
+ | In hence, we decide to make an App to teach them the basic biotech concept and let them know the synthetic biology is not so hazardous. The main idea of this game is let players know if they don‘t care about the biosafety, they will let environment endanger. But if they are cautious in their operation, most of the results will under their control. | ||
+ | </p> | ||
</div> | </div> | ||
<section class="red-background"> | <section class="red-background"> | ||
- | + | <h1 class="header">Cooperation</h1> | |
</section> | </section> | ||
+ | |||
<div class="container divide essay"> | <div class="container divide essay"> | ||
- | + | <ul style="list-style:style"> | |
- | + | <li> | |
- | + | Collaborate with Perdue iGEM team: <br/><br/> | |
- | + | <p>We collaborated with Perdue iGEM team to design a better version of datasheet when we register our parts. Following is one of the beta-version of their datasheet. </p> | |
+ | <embed src="./PDF/Datasheet Composite Part Example.pdf" style="width: 100%; height: 500px"></embed> | ||
+ | </li> | ||
+ | <br/> | ||
+ | |||
+ | <li>Kyoto iGEM team: <br/><br/> | ||
+ | <div class="row"> | ||
+ | <div class="col-md-7"> | ||
+ | <p>We help Kyoto iGEM team to charaterise their parts. They sent 13 parts to us. We keep discussing how to design the construction and which gene should we use in the characterisation.</p> | ||
+ | </div> | ||
+ | |||
+ | <div class="col-md-5"> | ||
+ | <img class="img-responsive" src="./images/Human_practice/HUMANPRACTICE_2.jpg" style="margin-right: 30px"> | ||
+ | </div> | ||
+ | </div> | ||
+ | </li> | ||
+ | |||
+ | <li>NTU_Taida iGEM team: <br/> | ||
+ | </ul> | ||
</div> | </div> | ||
</script> | </script> | ||
Line 1,126: | Line 1,193: | ||
</div> | </div> | ||
<div> Meeting </div> | <div> Meeting </div> | ||
+ | </a> | ||
+ | </div> | ||
+ | <div class="col-md-2 photo-item"> | ||
+ | <a class="pointer-cursor" scroll-to="Meeting2"> | ||
+ | <div class="row "> | ||
+ | <span class="icon-stack icon-4x"> | ||
+ | <i class="icon-stop icon-stack-base font-brown"></i> | ||
+ | <i class="icon-lightbulb icon-light"></i> | ||
+ | </span> | ||
+ | </div> | ||
+ | <div> Meeting2 </div> | ||
</a> | </a> | ||
</div> | </div> | ||
Line 1,159: | Line 1,237: | ||
</div> | </div> | ||
<div> LabTime </div> | <div> LabTime </div> | ||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
</a> | </a> | ||
</div> | </div> | ||
Line 1,190: | Line 1,257: | ||
<h1 class="header">Meeting Photos</h1> | <h1 class="header">Meeting Photos</h1> | ||
<p class="header container"> | <p class="header container"> | ||
+ | Leisure time | ||
</p> | </p> | ||
<div class="divide"> | <div class="divide"> | ||
<div class="row"> | <div class="row"> | ||
<ul class="tilt-gallery img-2x" lightbox-id="meeting"> | <ul class="tilt-gallery img-2x" lightbox-id="meeting"> | ||
- | <li><img src="./images/MEETING/(1).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(1).jpg" ></li> |
- | <li><img src="./images/MEETING/(2).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(2).jpg" ></li> |
- | <li><img src="./images/MEETING/(3).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(3).jpg" ></li> |
- | <li><img src="./images/MEETING/(4).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(4).jpg" ></li> |
- | <li><img src="./images/MEETING/(5).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(5).jpg" ></li> |
- | <li><img src="./images/MEETING/(6).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(6).jpg" ></li> |
- | <li><img src="./images/MEETING/(7).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(7).jpg" ></li> |
- | <li><img src="./images/MEETING/(8).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(8).jpg" ></li> |
- | <li><img src="./images/MEETING/(9).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(9).jpg" ></li> |
- | <li><img src="./images/MEETING/(10).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(10).jpg" ></li> |
- | <li><img src="./images/MEETING/(11).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(11).jpg" ></li> |
- | <li><img src="./images/MEETING/(12).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(12).jpg" ></li> |
- | <li><img src="./images/MEETING/(13).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(13).jpg" ></li> |
- | <li><img src="./images/MEETING/(14).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(14).jpg" ></li> |
- | <li><img src="./images/MEETING/(15).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(15).jpg" ></li> |
- | <li><img src="./images/MEETING/(16).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(16).jpg" ></li> |
- | <li><img src="./images/MEETING/(17).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(17).jpg" ></li> |
- | <li><img src="./images/MEETING/(18).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(18).jpg" ></li> |
- | <li><img src="./images/MEETING/(19).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(19).jpg" ></li> |
- | <li><img src="./images/MEETING/(20).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(20).jpg" ></li> |
- | <li><img src="./images/MEETING/(21).jpg" ></li> | + | <li><img src="./images/MEETING/Meeting-(21).jpg" ></li> |
+ | <li><img src="./images/MEETING/Meeting-(22).jpg" ></li> | ||
+ | <li><img src="./images/MEETING/Meeting-(23).jpg" ></li> | ||
+ | <li><img src="./images/MEETING/Meeting-(24).jpg" ></li> | ||
+ | <li><img src="./images/MEETING/Meeting-(25).jpg" ></li> | ||
+ | <li><img src="./images/MEETING/Meeting-(26).jpg" ></li> | ||
+ | <li><img src="./images/MEETING/Meeting-(27).jpg" ></li> | ||
+ | <li><img src="./images/MEETING/Meeting-(28).jpg" ></li> | ||
+ | </ul> | ||
+ | </div> | ||
+ | </div> | ||
+ | </section> | ||
+ | |||
+ | <section class="brown-background divide" id="Meeting2"> | ||
+ | <h1 class="header">Meeting Photos - Serious</h1> | ||
+ | <p class="header container"> | ||
+ | Serious | ||
+ | </p> | ||
+ | <div class="divide"> | ||
+ | <div class="row"> | ||
+ | <ul class="tilt-gallery img-2x" lightbox-id="meeting2"> | ||
+ | <li><img src="./images/MEETING_2/MEETING_1.jpg" ></li> | ||
+ | <li><img src="./images/MEETING_2/MEETING_2.jpg" ></li> | ||
+ | <li><img src="./images/MEETING_2/MEETING_3.jpg" ></li> | ||
+ | <li><img src="./images/MEETING_2/MEETING_4.jpg" ></li> | ||
+ | <li><img src="./images/MEETING_2/MEETING_5.jpg" ></li> | ||
+ | <li><img src="./images/MEETING_2/MEETING_6.jpg" ></li> | ||
+ | <li><img src="./images/MEETING_2/MEETING_7.jpg" ></li> | ||
</ul> | </ul> | ||
</div> | </div> | ||
Line 1,286: | Line 1,381: | ||
<li><img src="./images/Chiao_Tung_Conference/(31).jpg" ></li> | <li><img src="./images/Chiao_Tung_Conference/(31).jpg" ></li> | ||
<li><img src="./images/Chiao_Tung_Conference/(32).jpg" ></li> | <li><img src="./images/Chiao_Tung_Conference/(32).jpg" ></li> | ||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
</ul> | </ul> | ||
</div> | </div> | ||
Line 1,376: | Line 1,457: | ||
<b>Does your country have national biosafety regulations or guidelines? If so, please provide a link to these regulations or guidelines if possible.</b><br/><br/> | <b>Does your country have national biosafety regulations or guidelines? If so, please provide a link to these regulations or guidelines if possible.</b><br/><br/> | ||
<p style="margin-left: 40px">" http://esh.ntu.edu.tw/epc/e-home.php "<br/> | <p style="margin-left: 40px">" http://esh.ntu.edu.tw/epc/e-home.php "<br/> | ||
- | |||
This is also the biosafety guidelines that our institution follows.<br/> | This is also the biosafety guidelines that our institution follows.<br/> | ||
</p> | </p> | ||
Line 1,474: | Line 1,554: | ||
<section class="yellow-background"> | <section class="yellow-background"> | ||
<h1 class="header">Chassis</h1> | <h1 class="header">Chassis</h1> | ||
- | <p class="header"> | + | <p class="header"><i>Saccharomyces cerevisiae</i></p> |
</section> | </section> | ||
<div class="container divide essay"> | <div class="container divide essay"> | ||
Line 1,489: | Line 1,569: | ||
<div class="container divide"> | <div class="container divide"> | ||
<img src="images/e_coli.jpg" class="pull-right img-responsive"> | <img src="images/e_coli.jpg" class="pull-right img-responsive"> | ||
- | <p>The yeast <b>Saccharomyces cerevisiae</b> has several properties which have established it as an important tool in the expression of foreign protein for research, industrial or medical use. As a food organism, it is highly acceptable for the production of pharmaceutical proteins. In contrast, <b>Escherichia coli</b> have toxic cell wall pyroxenes and mammalian cells may contain oncogenic or viral DNA, so that products from these organisms must be tested hmore extensively.</p> | + | <p>The yeast <b><i>Saccharomyces cerevisiae</i></b> has several properties which have established it as an important tool in the expression of foreign protein for research, industrial or medical use. As a food organism, it is highly acceptable for the production of pharmaceutical proteins. In contrast, <b><i>Escherichia coli</i></b> have toxic cell wall pyroxenes and mammalian cells may contain oncogenic or viral DNA, so that products from these organisms must be tested hmore extensively.</p> |
- | <p>Yeast can be grown rapidly on simple media and to high cell density and its genetics are more advanced than any other eukaryote, so that it can be manipulated almost as readily as <b>E.coli</b>. As a eukaryote, yeast is a suitable host organism for the High-level production of secreted as well as soluble cytosolic proteins.</p> | + | <p>Yeast can be grown rapidly on simple media and to high cell density and its genetics are more advanced than any other eukaryote, so that it can be manipulated almost as readily as <b><i>E.coli</i></b>. As a eukaryote, yeast is a suitable host organism for the High-level production of secreted as well as soluble cytosolic proteins.</p> |
<hr/> | <hr/> | ||
<p>Most yeast expression vectors have been based on the multi-copy 2p plasmid and contain sequences for propagation in E.coli and in yeast, as well as a yeast promoter and terminator for efficient transcription of the foreign gene. The recent rapid expansion in yeast molecular genetics has led to a great increase in our understanding of these components, and as a result there is now a bewildering choice of promoter systems and methods for propagating foreign DNA in yeast. In many cases ingenious new approaches have been employed, for example in increasing the strength of native promoters or the stability of expression vectors. </p> | <p>Most yeast expression vectors have been based on the multi-copy 2p plasmid and contain sequences for propagation in E.coli and in yeast, as well as a yeast promoter and terminator for efficient transcription of the foreign gene. The recent rapid expansion in yeast molecular genetics has led to a great increase in our understanding of these components, and as a result there is now a bewildering choice of promoter systems and methods for propagating foreign DNA in yeast. In many cases ingenious new approaches have been employed, for example in increasing the strength of native promoters or the stability of expression vectors. </p> | ||
Line 1,538: | Line 1,618: | ||
<h1 class="header">Suicide</h1> | <h1 class="header">Suicide</h1> | ||
</section> | </section> | ||
- | <div class="essay container divide"> | + | <div class="essay container divide" style="margin-left: 40 px"> |
- | + |         In case of an accidental release of the thermogenic yeasts from our device to the environment, we have designed a kill switch that would ideologically lead the yeasts to death under such circumstance.<br/> | |
+ |         When faced with an increasing osmaolarity of the environment, the HOG pathway is activated in yeasts and the final result is the accumulation of glycerol in yeast cells to balance the exterior osmotic pressure. Sensors of the ambient osmolarity rise activates a MAPK cascade and eventually leads to the phosphorylation and activation of the Hog1 protein. Activated Hog1 then translocates into the nucleus and activates a number of transcriptional factors via protein-protein interactions or phosphorylation. These transcriptional factors (mostly activators) then mediate the expression of hundreds of genes related to cell integrity and adaptation to osmostress. Among these, the GPD1 gene and the STL1 gene are the most significant targets of the HOG pathway. GPD1 encodes the sequences for NAD-dependent glycerol-3-phosphate dehydrogenase, which is the key enzyme of glycerol sythesis. Following activation of the HOG pathway, activated Hog1 binds to the transcriptional acitvator Hot1 and upregulates the expression of GPD1. On the other hand, STL1 codes for a glycerol proton symporter in the plasma membrane of S. cerevisiae. Upon sensing a rise in osmolarity, STL1 is strongly and transiently induced by transcriptional activators Hot1 and Smp1, both members of the HOG pathway. Smp1 is phosphorylated and activated by the active Hog1 protein. Thus, the sensing of osmolarity and the induction of GPD1 and STL1 expression will make up mainly the fist part of our kill switch.<br/> | ||
+ |         In order to complete our kill switch so that increasing osmolarity not only activates the HOG pathway, but also leads to cell death, we further integrate a kill gene following the promoter sequence of GPD1 and STL1. The most suitable genes would be those encoding proteins that have nuclease activity. A couple of chosen examples are NUC1 (encoding endonuclease G) and YBL055C (encoding Tat-D nuclease). Endonuclease G is the major mitochondrial nuclease in S. cerevisiae, and it induces apoptosis in yeast independently of metacaspase or of apoptosis inducing factors. Tat-D is an endo-/exo-nuclease that incises the double stranded DNA without obvious specificity via its endonuclease activity and excises the DNA from 3' to 5' end by its exonuclease activity. These proteins are intrinsically expressed during apoptosis, and their induction via osmosensitive promoters would cause irreversible harm to the yeasts and in the end kill them.<br/> | ||
+ |         According to data from current milkfish farms in Taiwan, which are saltwater farms, water osmolarity is way higher than yeast culturing environments. Therefore the HOG pathway would surely be activated once the yeasts escape from the thermogenic device, with following cell death. If the device is to be used in a fish farm with fresh water, the osmolarity would very likely be lower than the yeast culture. In light of this possibility, we are also looking into another mechanism of S. cerevisiae that is used when it is subjected to low osmolarity stress. It is called the cell integrity pathway, and is activated upon decreasing osmolarity of the environment. We hope to find similar functioning effectors downstream of the pathway like we did in the HOG pathway, and integrate the activated promoters with kill genes. If succeeded, our safety design will not be restricted to saltwater fish farms.<br/> | ||
</div> | </div> | ||
</div> | </div> | ||
Line 1,568: | Line 1,651: | ||
<p><i><u>Rhodotorula</u></i> is pigment produce yeast quite easily identifiable by distinctive orange/red colonies when grown on SDA. This distinctive color is the result of pigments that the yeast creates to block out certain wavelengths of light that would otherwise be damaging to the cell. Colony color can vary from being cream colored to orange/red/pink or yellow.<br/> | <p><i><u>Rhodotorula</u></i> is pigment produce yeast quite easily identifiable by distinctive orange/red colonies when grown on SDA. This distinctive color is the result of pigments that the yeast creates to block out certain wavelengths of light that would otherwise be damaging to the cell. Colony color can vary from being cream colored to orange/red/pink or yellow.<br/> | ||
<i><u>Rhodotorula</u></i> is a common environmental inhabitant. It can be cultured from soil, water, and air samples. It is able to scavenge nitrogenous compounds from its environment remarkably well, growing even in air which has been carefully cleaned of any fixed nitrogen contaminants. In such conditions, the nitrogen content of the dry weight of <i><u>Rhodotorula</u></i> can drop as low as 1%, compared to around 14% for most bacteria growing in normal conditions. <br/> | <i><u>Rhodotorula</u></i> is a common environmental inhabitant. It can be cultured from soil, water, and air samples. It is able to scavenge nitrogenous compounds from its environment remarkably well, growing even in air which has been carefully cleaned of any fixed nitrogen contaminants. In such conditions, the nitrogen content of the dry weight of <i><u>Rhodotorula</u></i> can drop as low as 1%, compared to around 14% for most bacteria growing in normal conditions. <br/> | ||
- | + |         The increasing cost of vegetable oils is turning the use of microbial lipids into a competitive alternative for the production of biodiesel fuel. The oleaginous yeast <i><u>Rhodotorula glutinis</u></i> is able to use a broad range of carbon sources for lipid production, and is able to resist some of the inhibitors commonly released during hydrolysis of lignocellulose materials. <br/> | |
- | + |         So we choose R.g. for the Expression vector.<br/> | |
- | + |         Thermogenic yeast relies on cultural media to grow and to generate heat. This way, the Yeastherm is kind of like burning media as fuel, which is expensive compared with other heating methods such as gas, coal, or electricity. To make our project a more competitive choice when considering large-scale heat production such as heating up a pound in the winter, it is necessary to reduce the cost of culturing yeast. Thanks to previous study in the field of biofuel, we have several solutions of cheaper substitutions of cultural medium contents.<br/> | |
- | + |         According to Jie Tao and his colleague’s study, agricultural and forestry residues can be used as an alternative of carbon source, taking advantage of <i><u>Rhodotorula glutinis’s</u></i> ability to assimilate xylose. Agricultural residues such as rice straw and corn stalk are usually burned after harvest. Using these materials not only lower the expense but also benefits the environment. Raw materials like rice or wheat straw are first cut into pieces of appropriate size. They are then hydrolyzed using sulfuric acid with boiling water bath, turninig into hemicellulosic hydrolyzate. Saccharides can be obtained in supernatant after centrifugation and washings of the residue with hot water. <br/> | |
- | + |         After expressing SrUCP in <i><u>Rhodotorula glutinis</u></i>, we will test for appropriate concentration for Agricultural residue extraction considering growth condition and heating power. The optimized heat power will then be used in large scale simulation as well as calculation of cost reduced. If time permitted, we will dig further into the component of the hemicellulosic hydrolyzate, as it is reviewed that there might be inhibiting compound.<br/> | |
</div> | </div> | ||
</div> | </div> |
Revision as of 16:45, 26 September 2013
<!DOCTYPE html>