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State University San

Location:
El Cajon, CA, 92021
Posted:
March 09, 2010

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Resume:

COURTNEY A BENSON

**** ***** ****

El Cajon, CA *2021

619-***-****

****************@*****.***

EDUCATION

San Diego State University, San Diego, CA

M.S. in Cell and Molecular Biology, Master's Thesis Manuscript completed

December 2009, Graduation May 2010

Master's Thesis: Microbial Diversity in Steam Vent Sublimates

Thesis Advisor: Dr. Richard Bizzoco

San Diego State University, San Diego, CA

B.S. in Cell and Molecular Biology, May 2007

SKILLS

Specialties

Environmental DNA extraction, 16S rRNA gene amplification, and cloning

Cultivation of extremophiles

Laboratory

Steam Microbiology: Culturing novel archaea and bacteria, DNA extractions,

polymerase chain reaction (PCR), environmental DNA extractions (archaea and

bacteria), gel electrophoresis, DAPI staining, microscopy, DNA sample

preparation for sequencing, and cloning. Collaborative chemistry: ICP-OES

elemental analysis, nutrient analysis and x-ray microanalysis of

environmental steam sediments.

RESEARCH EXPERIENCE

Graduate Research, Dr. Richard Bizzoco and Dr. Scott T. Kelley,

Microbiology, San Diego State University, San Diego, CA

June 2007- December 2009

Steam Sublimate Microbiology

Fumaroles, commonly called steam vents, contain diverse microbial

communities. Fumaroles occur when steam and volcanic gases escape through

Earth's crust as a result of magma degassing and/or geothermal heating of

groundwater aquifers at a shallow depth (Costello et al 2009). In my study,

steam sublimates were analyzed for archaeal and bacterial DNA. As the steam

approaches and exits a vent or cave, minerals with microorganisms are

deposited along the cooler walls and ceilings as steam sublimates. During

the summer of 2008, I had the opportunity to travel to Yellowstone National

Park to conduct field research, collect samples for my study, and discover

new steam caves with unknown archaea. Processing the samples for my study

proved to be difficult; steam sublimates are highly acidic. I developed a

singular method to allow a more efficient DNA yield for environmental

extractions. After DNA extraction, I amplified the DNA by polymerase chain

reaction (PCR) and visualized the amplified DNA by gel electrophoresis.

Once all DNA extractions were completed, I processed the samples by TOPO TA

Cloning . From the resulting archaeal sequences, I generated a phylogenetic

tree as part of my analysis of the results. The bacterial sequences were

analyzed; many diverged significantly from sequences of known organisms.

The second part of my study involved the cultivation of archaea and

bacteria in liquid media and on solid media agar and Gelrite overlays. The

positive cultures were extracted for DNA, and after purification were

amplified by PCR. The amplified DNA was visualized by gel electrophoresis

and sent out for sequencing. Phylogenetic trees will be created from the

resulting archaeal and bacterial sequences. During this study I developed a

new DNA extraction method for archaea and discovered and cultured several

unknown archaea. My manuscript will be submitted for publication in

December 2009.

Undergraduate Research, Dr. Richard Bizzoco, Microbiology. San Diego State

University, San Diego, CA.

August 2006- May 2007

Steam Microbiology

I began my research in Dr. Richard Bizzoco's laboratory learning the basics

of molecular biology. I started by culturing archaea and bacteria from

steam samples condensed aseptically from fumaroles, to provide assistance

and data for a graduate student research project. After successfully

growing organisms in liquid media and on solid media, I was able to extract

the DNA using the lysozyme method. I then PCR amplified and visualized the

DNA by gel electrophoresis. Once DNA samples were ready for sequencing, I

prepared and sent off the purified PCR products to the MicroChemical Core

facility at SDSU and was able to identify the species by phylogenetic

analysis, using several databases and software programs for base calling

and alignments. My most interesting and unexpected finding was that I was

able to grow halophilic archaea from Yellowstone National Park steam

samples nearly devoid of salt (Ellis et al 2008).

TEACHING EXPERIENCE

Teaching Assistant, San Diego State University, San Diego, CA

August 2008- December 2009

. Developed instructional plans and taught an advanced level laboratory

course in Principles of Cell and Molecular Biology.

. Guided several undergraduates and assisted with orientation to

molecular and cellular research in our laboratory over a period of

years. A current student is working on fluorescent in situ

hybridization (FISH) for my steam sediment project.

PRESENTATIONS

Posters

. Presented at 2009 Student Research Symposium: Microbial Diversity in

Steam Vent Sublimates. San Diego State University. February 27, 2009.

. Co-Author for poster presented at 2008 Annual Biomedical Research

Conference for Minority Students: Subsurface Microbiology: Growth of

Organisms Recovered from Volcanic Steam Sublimates. November 11, 2008.

. Presented for Rhetoric and Writing Studies: Steam Microbiology: What

is it? San Diego State University. November 3, 2008.

. Presented at the Undergraduate Research Symposium: Subsurface

Microbiology: Growth of Organisms recovered from Volcanic Steam. San

Diego State University. April 20, 2007.

Powerpoint Presentations

. Microbial Diversity in Steam Vent Sublimates. Thesis Defense, San

Diego State University. December 10, 2009.

. Immune response against frameshift-induced neopeptides in HNPCC

patients and healty HNPCC mutation carriers, Schwitalle et al 2008.

San Diego State University, partner presentation. March 25, 2009.

. Melamine and food safety in China. San Diego State University.

February 23, 2009.

. Microbial diversity in steam vent sublimates. Thesis Proposal, San

Diego State University. November 20, 2008.

. Why are parasite contingency genes often associated with telomeres?

J.D. Barry et al 2003. San Diego State University. May 9, 2008.

. An intronic element contributes to splicing repression in spinal

muscular atrophy, Kashima et al 2007. Group presentation, San Diego

State University. April 2008.

. Li Fraumeni. Group presentation, San Diego State University. April

2008.

. Essential role for Dicer during skeletal muscle development, J.R.

O'Rourke et al 2007. Group presentation, San Diego State University.

February 4, 2008.

. The crystal structure of ?-Gam protein suggests a model for RecBCD

inhibition, Robert Court et al 2007. Partner presentation, San Diego

State University. September 24, 2007.

AWARDS

. Mabel Meyers Memorial Scholarship. 2009-10.

REFERENCES

Richard Bizzoco, Ph.D. Scott Kelley, Ph.D.

Department of Biology Department of Biology

San Diego State University San Diego State University

South Life Sciences 362 South Life Sciences 373

5500 Campanile Drive 5500 Campanile Drive

San Diego, CA 92182 San Diego, CA 92182

********@********.****.*** *******@********.****.***

619-***-**** 619-***-****

David Truesdale Anca Segall, Ph.D.

Lab Coordinator Department of Biology

San Diego State University San Diego State University

Physical Sciences 230 North Life Sciences 331

5500 Campanile Drive 5500 Campanile Drive

San Diego, CA 92182 San Diego, CA 92182

********@*********.****.*** *******@*********.****.***

619-***-**** 619-***-****



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