Am I a biohazard?![]() Foreign genes expressed in glowing E. coli, the result of the
evening’s DIYbio experiment.
Courtesy of Ellen Jorgensen
Brooklyn, New York, April 21, 19:00 hours: Molecular biologist Ellen Jorgensen and I spread a plastic tarp over my cherry table and parquet floor. Then, one by one, we set vials and pipettes down, preparing a lab in my living room. We had dubbed it DNA and Pizza Night on the DIYbio message board, inviting aspiring amateur geneticists to gather and learn the rudiments of bioengineering. Not a bad deal either—a lab followed by beer and pizza, all for $10 per person. As the aficionados and the curious made their way to my Brooklyn home, Jorgensen and I laid out our genetic-makeover patient, a sealed Petri dish of E. coli. It was our first meeting working with live bacteria, and it had already taken on an illicit air. In May, The Wall Street Journal asked whether amateur gatherings like ours were “a threat to national security.” The Boston Globe cautioned that do-it-yourselfers raised “fears that people could create a deadly microbe on purpose.” And an article in Systems and Synthetic Biology warned that we might engineer bacteria to produce cocaine in the way that bacteria are now being used to produce antimalarials (Syst Synth Biol, 2:1–6, 2008). DNA and Pizza Night, a cocaine ring? It all seemed a little far-fetched. But the week of our gathering, reporters were already calling and emailing, including one from The New York Times Magazine, who asked to join us for the event. For my own part, I’d gone to the first meeting of the New York DIYbio chapter at a diner on the Upper West Side out of curiosity. When only four of us came, I’d become a founding member by default. It wasn’t a bad deal—a lab followed by a beer and pizza, all
for $10 per person.
Ten people showed up that night, including a lawyer, physics student, installation artist, architect, and three reporters. Feeling slightly tense under the reporters’ scrutiny, we circled around Jorgensen, an assistant professor of clinical research at New York Medical College, as she used a loop to collect colonies of the innocuous K-12 strain of E. coli from the Petri dish and deposit them in an iced vial of calcium chloride. This was the first step in cajoling the bacteria into accepting a new set of DNA instructions, providing us with an opportunity to teach our small audience about lab safety and basic principles of genetic engineering. We’d eventually graduate into creating something new. For now, our materials came from a high school biology lab teacher’s kit. Amateur bioengineers suffer from an image problem. We operate outside the confines of an academic institution in a science that is bounding ahead of legislation, not unlike the International Genetically Engineered Machine (iGEM) competition at MIT. Every summer, college teams are sent toolkits of DNA parts, a lot like sets of biological Lego bricks, and asked to build something new and beneficial. Last year, the winner created a vaccine for ulcers. It’s not a coincidence that a former iGEM staffer, Mackenzie Cowell, cofounded our umbrella organization, DIYbio. But it came as a blow when the iGEM leadership disqualified the group from entering this year’s competition. Their reasons were many, but one had an all too familiar ring: amateur teams were a liability until they could vouch for the safety of their projects. “We had to think about safety infrastructure,” iGEM’s assistant director Meagan Lizarazo told me. Groups like ours were crippled without access to iGEM’s toolkit of DNA parts. No one was harmed at my apartment though, not even a burn. K-12 E. coli has been a favorite in labs since 1922 because it’s unable to compete with wild E. coli and safe enough to handle without gloves. After 15 minutes on ice, we shifted the vial into a bowl of 42-degree Celsius water, and heat shocked the E. coli for 90 seconds. The temperature shift opened the pores on its membrane, allowing foreign DNA containing GFP to slip inside. A few minutes later, we smeared the bacteria onto a fresh Petri dish. The 2-hour lab complete, the last thing left to do was eat pizza. We disposed of our materials in a bucket of bleach and moved to the kitchen. Jorgensen took the resultant Petri dish home with her to incubate. Two days later, she emailed us all a snapshot for the album: under black light, our E. coli glowed like little green pearls. Advertisement
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Pirate Scientists, I'm on your side! by Jessica Fryer [Comment posted 2009-08-18 18:29:09] I think I'd personally prefer amateur astronomy night.
But I don't see how science conducted within the walls of a prestigious university is somehow more scientific than science conducted anywhere else in the world. Obviously academia is getting intimidated. BioBadBoy by Hill Maggie [Comment posted 2009-08-17 17:43:53] The author sounds like an interesting, intelligent, somewhat twisted character. But not a hazard. Good stuff. FYI -- Sky News article dated 01 August 09 by TS Raman [Comment posted 2009-08-15 01:43:35] LINK
"DIY DNA: ?Biohackers? Creating Own Bugs -- 12:50pm UK, Saturday August 01, 2009 by Thomas Moore, health correspondent, Sky News" "Amateur scientists are creating mutant microbes in labs they've set up in their own homes with the help of Ebay and YouTube.The growing group of self-styled ?biohackers? say they are creating the genetically-engineered bugs in makeshift gene laboratories for fun....[etc.]" A better critique is needed by Mike Serfas [Comment posted 2009-08-14 18:28:11] The original Systems and Synthetic Biology article is freely available (LINK but I am disappointed with its reasoning.
The cocaine scenario Schmidt suggests is that interested amateurs would produce the drug in the way that artemisinin derivatives are produced in bioengineered yeast. Engineered production of a precursor, artemisinic acid, is a bold idea intended to cut production costs well below the current rate of $2.20 per adult course of treatment. (See LINK ) Even so, three years after the 2006 publication in Nature, with major ongoing support from the Gates charity fund, the process is still under development. I don't think that it is reasonable to worry that a few amateurs working with plasmids in E. coli will be able to compete economically against large plantations of coca. The current method of production converts water and sunshine into nearly 1% of cocaine, which can be extracted with organic solvents without regard for environmental impact. Schmidt raises other curious concerns, such as viral total synthesis, which could not readily be accomplished without professional equipment, and creation of "new life forms or biological systems", which except in hyperbole could not readily be accomplished with professional equipment. He speaks of "bio-spam, bio-spyware, bio-adware". I think he has gotten a bit ahead of the class. It is true that there are real concerns that can come up from amateur biology, but they are at a lower level of technology. If efforts to synthesize cheaper artemisinin-related drugs do not succeed, perhaps some in malarial countries will choose to farm their own sweet wormwood to use directly for its artemisinin as in the time of Ge Hong, and some may ask whether this would make it easier for the parasite to develop resistance than use of (relatively) expensive, imported, patented multidrug mixtures. We might ask whether careless use of plasmids with antibiotic resistance genes could pose a health threat to those who work with them. And of course the same rules for limiting dangerous pathogens to BSL rated facilities apply to amateurs as to professionals. But it is absurd to suggest that biology must be irresponsible or unethical solely because it is not done by associates of a university or corporation. Other articles by Alison McCook [Comment posted 2009-08-04 16:23:19] One article from a journalist at the event has been published: LINK
The New York Times has yet to publish anything on the event. We'll keep you posted. Alison McCook Deputy Editor And...? by anonymous poster [Comment posted 2009-08-04 14:57:47] Don't keep us in suspense - did any of the three reporters publish an article, and if so, what did they say? I'd guess that they were disappointed that your mutant bacteria failed to grow into a hideous giant creature before their very eyes and scale the Empire State Building, and so they left looking for a better story.
I'd love to be told that didn't happen, though... |
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