User:ShLo

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(What I'm Currently Reading:)
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Stephanie Lo <br>
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Harvard College 2010
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<Br><Br>
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1885 Harvard Yard Mail Center<br>
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Cambridge, MA 02138
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I have always had a passion for sciences, particularly chemistry, and hope to pursue a joint concentration in Molecular and Cellular Biology and Economics. Eventually, I plan to apply for an MD/PhD program and specialize in digestive disorders.
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<b> Latest news: </b><br>
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I'll be making a presentation at the next iGEM meeting on engineering <i>E.coli</i> to efficiently produce EtOH as well as adaptamers (past studies of, and potential applications of). Adaptamers haven't been at the forefront of discussion lately, but they're great for labs of the iGEM size, and have an array of potential uses. <br>
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[http://openwetware.org/wiki/Image:SLoAdaptamerHandout.doc Presentation Handout]
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== What I'm Currently Reading: ==
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<i> Note: I'm not formatting my citations correctly, I know. If there is any confusion, please let me know. Also, though some of the articles do not have links, they should be readily accessible via PubMed with a Harvard login. </i>
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<b>Engineering for EtOH production</b>
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Ingram L, et al. 1987. Genetic engineering of ethanol production in E. coli. Applied and Environmental Microbiology. 53, 10: 2420-2425. [http://aem.asm.org.ezp1.harvard.edu/cgi/reprint/53/10/2420?view=long&pmid=3322191 Full text]
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Perhaps one of the oldest papers, but also one of the best in terms of examining the basic engineering concepts that the other papers seem to take for granted.
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Ohta K, et al. 1991. Genetic Improvement of E. Coli for Ethanol production: chromosomal integration of Z. mobilis genes encoding pyruvate decarboxylase and alcohol dehydrogenase II. Applied and Env Microbio, 57, 4: 893-900. [http://aem.asm.org.ezp1.harvard.edu/cgi/reprint/57/4/893?view=long&pmid=2059047 full text]<br>
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Looks intriguing. Again, relatively old, but I think it will emphasize basic manipulations that have been experimentally performed - which is good if we plan to look into this. I haven't read this one fully yet, but I'll update if I do. <br><br>
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Rao K, et al. 2007. Enhanced ethanol fermentation of brewery wastewater using genetically modified strain E. coli KO11.<br>
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Two major results should be emphasized: yeast consistently produced EtOH more rapidly; commericial enzymes (alpha-amylase and pectinase) enhanced EtOH yields in both yeast and e.coli. As a side note, I'm finding it interesting that most of the newer articles (such as this one) seem to advocate using engineered yeast rather than e.coli, while many earlier studies (early 1990s) seemed to find that E. coli were equally, or more, efficient. I'll keep an eye out for this trend as I continue reading. <br>
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Stephanopoulos, G. Challenges in engineering microbes for biofuels production. 2007, Science, 315, 801. <br>
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Easily readable, but not extremely pertinent to the engineering of <i> E. coli</i> that we've been considering.
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<br>Service, R. CELLULOSIC ETHANOL: Biofuel Researchers Prepare to Reap a New Harvest. <i> Science </i> 16 March 2007. Vol. 315, no 5818, 1488-1491.[http://www.sciencemag.org.ezp1.harvard.edu/cgi/content/full/315/5818/1488 Full Text; requires login]
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<br> This paper isn't as mechanism-based as the Aristou paper (cited below), but provides a nice overview of the history of ethanol use, why energy is a concern, etc. It seems to be a nice background for the general public, and provides a nice introduction to the field.
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Aristidou, A and M Penttila. Metabolic engineering applications to renewable resource utilization. <i> Science Direct: Current Opinion in Biotechnology </i> 1 April 2000. Vol 11, no 2, 187-198. [http://www.sciencedirect.com.ezp1.harvard.edu/science?_ob=ArticleURL&_udi=B6VRV-40199MT-J&_user=209690&_coverDate=04%2F01%2F2000&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000014438&_version=1&_urlVersion=0&_userid=209690&md5=c0db238ba5445c41b1bda11384ac0a2f Full text]
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<br> This review focuses on the bioconversion of the pentose fractions into ethanol and suggests use of biocatalysts (such as bacteria and yeast) to assist in this slow-step in the conversion of sugars into useful products.
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<b> Adaptamers</b>
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<br> <i> Don't get intimidated by this list - I did a lot of this reading last semester for my research course over a period of a few weeks. The most pertinent ones are the ones that focus on adaptamers - such as the Reid PCR paper - and even those that focus on aptamers, since many of the potential applications parallel those of adaptamers. </i>
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Postier, et. al, “The construction and use of bacterial DNA microarrays based on an optimized two-stage PCR strategy”. BioMed Central Genomics, 2003; 4:23. <br>
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Erdeniz, et. al, “Cloning-Free PCR-Based Allele Replacement Methods”. Genome Research, 1997; 7: 1174-1183. <br>
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Rimmele, Martina, “Nucleic Acid Aptamers as Tools and Drugs: Recent Developments”, ChemBioChem, 4, 963-71. <br>
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Smalley and Ley, “L-selectin: Mechanisms and Physiological Significance of Ectodomain Cleavage.” Journal of Cellular and Molecular Medicine, 2005; 9.2: 255-66. <br>
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Fors, et. al, “L-Selectin Shedding Is Independent of Its Subsurface Structures and Topographic Distribution”. The Journal of Immunology, 2001; 167: 3642-51. <br>
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Hafezi-Moghadam A, et. al., “L-selectin shedding regulates leukocyte recruitment”. Journal of Experimental Medicine 2001; 193: 863-72. <br>
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Dong, et.al., “Mechanisms for Induction of L-selectin Loss from T Lymphocytes by a Cryptococcal Polysaccharide, Glucuronoxylomannan”. Infection and Immunity, 1999; 67: 220-9. <br>
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Norman KE, et al, “Peptides derived from the lectin domain of selectin adhesion molecules inhibit leukocyte rolling in vivo”. Microcirculation, 1996; 3: 29-38. <br>
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Reid, et. al, “Cloning-Free Genome Alterations in Saccharomyces cerevisiae Using Adaptamer-Mediated PCR”. Methods in Enzymology, 2002; 350: 258 -77. <br>
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Guo, et. al, “A New Technique for the Isolation and Surface Immobilization of Mesenchymal Stem Cells from Whole Bone Marrow Using High-Specific DNA Aptamers”. Stem Cells, 2006; 24: 2220-31. <br>
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Dellaire, et. al, “In situ imaging and isolation of proteins using dsDNA oligonucleotides”. Nucleic Acids Research, 2004; 32: 20. <br>
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Harvard iGEM team. http://parts2.mit.edu/wiki/index.php/Harvard_2006 <br>
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Spertini, et. al, “ELISA for quantitation of L-selectin shed for leukocytes in vivo”. Journal of Immunological Methods, 1992; 156: 115-23. <br>
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Schmuke and Welply, “A Method for Measuring Leukocyte Rolling on the Selectins.” Analytical Biochemistry, 1995; 226: 197-201. <br>
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Ley, et. al, “Lectin-like adhesion molecule 1 mediates leukocyte rolling in mesenteric venules in vivo.” Blood 1991; 77: 2553-55. <br>
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Norman KE, et. al, “Peptides derived from the lectin domain of selectin adhesion molecules inhibit leukocyte rolling in vivo.” Microcirculation. 1996; 3: 29-38. <br>
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Reid, et. al, “Efficient PCR-based gene disruption in Saccharomyces strains using intergenic primers”. Yeast 2002; 19: 319-28. <br>
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Reference website: Intergenic Primer Search Page. http://rothsteinlab.hs.columbia.edu/projects/primersearch.html. Rothstein Laboratory of Columbia University. Last Accessed: 22 December 2006.
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<b>General</b>
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Current Research Activity in Biosensors. Nakamura et al, 2003, Analytical Bioanalytical Chem. <br>
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A really great overview of some potential applications of biosensors, including electrochemical sensors, detergent sensors, acid rain sensors, red tide, cyanide sensors, E. coli used for gas toxicity monitoring (see reference 276 of the paper - I intend to look into this more), and food sensors to detect glucose, sucrose, and lactose.
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[http://openwetware.org/wiki/IGEM:Harvard/2007 Harvard iGEM]
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Current revision

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