Thursday, January 5, 2012

GC-MS brings SD-CAB into the 23rd Century

By Spencer Diamond

If captain James T. Kirk from the Star Trek series could come to the 21st century and help us develop biofuel he would likely bring with him one very cool piece of sci-fi technology, the Tricorder! SD-CAB scientists would find this fictional device particularly useful as it can scan living organisms and provide a wealth of information, including: size, shape, species, and molecular composition. With technology such as this one Scientists could even screen many different microbial mutants for, say, the molecular composition of their lipids. By doing so Kirk’s future sci-fi device would make it possible to find out how mutating various genes changes an organisms’ overall lipid profile to be more favorable for downstream biofuel production. Well, Kirk, you should probably just beam right back to the 23rd century, because SD-CAB has acquired an advanced piece of analytical technology that allows researchers to do just such an analysis.
Agilent 7890 GC-MS
            Roughly six months ago SD-CAB purchased a Gas Chromatograph-Mass Spectrometer (GC-MS). This instrument is commonly used in drug detection, environmental analysis, and anywhere it is necessary to specifically identify individual compounds in a complex mixture. The principals of GC-MS operation are suggested by its name, as it is in fact the marriage of two common analytical chemistry techniques: Gas Chromatography and Mass Spectrometry. Assume you have a complex sample such as a bacterial extract. First it would be necessary to separate all the compounds in the extract from each other via gas chromatography. The machine first heats the complex mixture to a point that all of the compounds in the mixture vaporize. The compounds, now in the gas phase, travel through a very long (up to 60 meters) tube known as a capillary column. In this tube the chemical and physical properties of the compounds cause them to move at different speeds separating them from each other over the tubes distance. One can think of it like a marathon, where a large group of people cluster at the start but the different speeds and stamina of the individuals cause them to spread out and cross the finish line individually.
As compounds exit the column they enter the mass spectrometer, and the analytical part of the process begins. Here each compound is hit with high energy causing it to fragment into a number of charged ions. The ions then pass through an electromagnetic field where they separate from each other. Finally, they impact on a detector that measures their mass and produces the “mass spectrum”. Here’s the cool part, almost every specific compound will fragment into the same ions every time. Thus, if you take the mass spectrum and compare it against a dictionary of mass spectra, it is possible to figure out exactly what compound you have in your sample. Also, because the GC-MS measures mass, not only can we identify the compounds, but we can also figure out how much is there.
            SD-CAB researchers have leaped into the future, quickly putting this new technology to use. Will Ansari, a graduate student in the laboratory of Prof. Steven Mayfield, has been mutating random genes in the Chlamydomonas reinhardtii genome to look for mutations that change the lipid content. Mutants that show changes in lipid content are analyzed by GC-MS to determine if there are changes in the overall lipid profile. His project will hopefully identify genes that affect the lipid profile of these cells. Understanding how the genetics of Chlamydomonas effects what types of lipids it produces will help engineers design algal strains with better lipid profiles for biodiesel or other industrial products.
Mass spectrum of methyl dodecanoate (a fatty acid)
Another SD-CAB graduate student, Christine Shulse of Prof. Eric Allen’s laboratory, has been specifically looking at the production of polyunsaturated fatty acids in bacteria (like the omega-3s we often are told to eat). These fats have high values as nutraceuticals, and may also be able to be produced as co-products during the synthesis of fuels or industrial chemicals. It was originally understood that only a small subset of marine bacteria had the genes necessary to produce polyunsaturated fatty acids, however Christine’s work has demonstrated that up to 10 different bacterial phyla have related clusters of genes, not know before, that likely perform the same process. The real mystery is that we do not know what types of fats these newly discovered genes are producing! Currently Christine has been trying to determine how growth conditions effect the polyunsaturated fatty acid synthesis. Using GC-MS she is identifying and quantifying the polyunsaturated fatty acids produced in bacteria under varying growth conditions. Future work in the laboratory will focus on many of the novel gene clusters discovered in her study, and use GC-MS to identify the different types of fatty acid molecules that are being produced by these novel gene clusters.
            As is evident from the above examples the GC-MS is an amazing device reminiscent of a sci-fi scanner. Unfortunately it still does not have the ability to translate alien languages or give telemetry data. Nonetheless, it looks like the future is approaching faster than we thought…Take that Tricorder!




Spencer Diamond is a graduate student at UCSD and a guest blogger and volunteer with SD-CAB. You can contact him at sdiamond@ucsd.edu. 

Wednesday, December 14, 2011

SD-CAB Researcher Spotlight - Susan Golden, Ph.D.

By Amanda Herman


Susan Golden is a member of the Faculty of 1000 Biology, a Fellow of the American Academy of Microbiology, and a Member of the National Academy of Sciences. In addition, she runs a lab at UCSD that studies circadian rhythms of gene expression in cyanobacteria. Golden summarizes her graduate school and postdoc experiences, how cyanobacteria are useful in the production of biofuels and how SD-CAB has shaped the direction of her research in this month’s SD-CAB Researcher Spotlight.

How did you decide that studying cyanobacteria was your passion?

I grew into it. I started working on cyanobacteria as a grad student. I wanted a "recombinant DNA" project, and when I started grad school in 1978, such approaches were still new and not used in most labs. I had a chance to join a lab in which the PI (Lou Sherman) had just done a sabbatical to learn basic molecular cloning methods with the idea of capitalizing on the then-recent discovery of a transformable cyanobacterium. My job was to develop a cloning system for that species, Anacystis nidulans R2, now known as Synechococcus elongatus PCC 7942, with the idea of using it to discover new genes involved in photosynthesis. Later I chose to do my postdoc in Bob Haselkorn's lab not so much because he worked on cyanobacteria, but because he was researching transcriptional regulation. I had expected to change organisms and research directions, but when I got there I still had "one last thing" I wanted to do from a loose end of my PhD work, and I ended up finding interesting new directions with S. elongatus. Thus, I just continued my PhD work on through my postdoc and into my independent research lab. The areas of emphasis and technologies have changed over the years, but I'm still working on my favorite little bug, the Anacystis that I was among the first to work with genetically. Being at the right place at the right time is my forte. I literally walked into Sherman's lab, while he was on sabbatical, within seconds of his postdoc writing (snail mail back then) to Lou: don't overlook the contribution a graduate student could make to this project.

How do cyanobacteria fit in with the production of biofuels?

Initially cyanobacteria were dismissed as biofuel organisms because they don't naturally store carbon as neutral lipids (oil droplets) that are easily converted to biodiesel. However, cyanobacteria are easier to genetically modify than are eukaryotic algae, and they can be engineered to make designer chemicals. Many species have growth advantages as crops: filamentous forms that are easy to harvest, some fix nitrogen, and they can grow at high pH conditions that kill off a lot of invading or grazing pests. Moreover, new biomass conversion technologies are making it possible to get useful hydrocarbons from biomass without requiring neutral lipids as a starting point. Thus, cyanobacteria can contribute in many ways to the enterprise.

What advice would you give to students interested in pursing research in academia?

Do it only if you love it. The challenge is that you have to constantly raise money just to do your job (to fund your lab), and many people end up depending on you to provide their salaries. That's a lot of pressure. However, it is fantastic to have the freedom to choose what to study (within reason), and to see the transformation that occurs in a student from the time he or she enters the lab to when they leave (as a scientist!).

What do you like to do in your spare time?

I like to read good novels. I'm open to a lot of genres, but they really need to be well written, with good character development and good use of language.


If you could have one famous scientist over for dinner (living or deceased), who would it be?

I think George Washington Carver would be a fascinating dinner companion.


How has SD-CAB helped further the success of your laboratory?

Being part of SD-CAB has swept me into applied microbiology and alliances with biotech companies. I'm learning a lot, and doing more as part of the group than I would have done on my own. I'm engaging in collaborations that I wouldn't have assembled on my own. The activities and interactions, and the growing reputation of SD-CAB around the world, are all good for my research program and for forcing me to expand my scientific horizons.


Amanda Herman is Ph.D. candidate at UCSD and a volunteer writer and outreach coordinator with SD-CAB. You can contact her at abherman@ucsd.edu.