Check out some of the gorgeous art people can make in petri dishes.
Clearly the people who create these have far steadier hands than I do when it comes to smearing out colonies.
Check out some of the gorgeous art people can make in petri dishes.
Clearly the people who create these have far steadier hands than I do when it comes to smearing out colonies.
Sorry for missing my daily post yesterday. Still trying to get over whatever I caught last week.
Last week, 13.3 million people watched CSI Miami in prime-time. That’s more people than live in the state Illinois. It doesn’t consider reruns, Tivo recordings, or piracy.** So to the untrained eye (mine), it seems likely the show is making enough money to hire a scientific consultant or two. Clearly the untrained eye is wrong and budgets are so tight that that the expense of finding someone who’d taken intro biology anytime in the past fifteen years was far too much. As demonstrated in this weeks episode “Bad Seed.”
Before I continue, let me say first of all I’m not one of CSI:Miami’s regular viewers. They don’t have to worry about losing me as a fan. I never was one. Second, I don’t get angry when shows like Fringe or the SyFy (<–that’s really how they spell their name now) Channel’s disaster and/or monster movie of the week completely mangle science. They are, and acknowledge themselves to be, science fiction. Shows based on fictional science. On the other hand, shows such as the CSI and Law&Order families set fictional stories in what, we are supposed to believe is, the real world. As such, the burden on them to get their facts straight is much stronger.
A burden the writers of CSI Miami clearly can’t be bothered to live up to. (Oh, if it wasn’t obvious already, spoilers ahead). (more…)
A lot of people may not share my enthusiasm for the potato genome, hopefully you all enjoy eating potatoes. The stereotype of potatoes is lots of boring sameness one identical to the next.* Reality, as usual, is much more complicated. Tens of thousands of cultivars can still be found in the South American regions where potatoes were first domesticated. In America, breeders are constantly working to bring in desirable traits from those (often really cool looking) breeds and even wild relatives of the potato. They face both genetic barriers (species barriers are bad enough normally, but trying to introgress genes across a tetraploidy can be a mess) and consumer acceptance ones.
This was driven home in a story at the NYtimes about Cornell potato breeders who have developed breeds which grow much better in upstate New York, but run into problems because the potatoes look and taste different than the couple of varieties of potatoes consumers and restaurants are used to (most notably Idaho grown Russet Burbanks**). Cornell Extension has been working on overcoming that barrier providing the potatoes to restaurants and, in what I think is a genius move, culinary schools throughout the region.
If you happen to visit New York farmers markets take a moment to ask sellers about the breeds of potatoes they have for sale.*** The potatoes covered in the story are Salem, Eva (both white potatoes), Lehigh, Keuka Gold (yellow breeds), Adirondack Blue and Adirondack Red (both of which are just the color you’d expect from the name.) Purple potatoes in particular just look really cool, see image above.
*There was a saying about accepting differences that I vaguely remember from a childhood TV show, something along the lines of “People aren’t the same like potatoes, and that’s a good thing because potatoes are boring.”
**The Russett Burbank was developed by a truck gardener outside of New York City called Luther Burbank in the 1800s who was initially inspired to become involved in plant breeding by Charles Darwin’s 1868 The Variation of Animals and Plants Under Domestication. He later moved to California where he became famous plant breeder and, among other things championed the practice of grafting (connecting a cutting from one plant (usually a tree) to the stem of another, which, if done properly grows the two together and the cutting will grow flower and produce fruit like it would normally) a practice at the time condemned as unnatural. <– This info from Mendel in the Kitchen by Nina Fedoroff and Nancy Brown a great resource
***In fact, whenever you’re buying directly from a farmer, if you get a chance, ask about the breed of whatever you’re buying. More often than you’d expect there’s an interesting story about why he or she is growing that particular breed and where it came from.
I’m sure everyone reading this has heard the term ‘superweed.’ These are the terrible new creations that will, or in some cases have, been created by herbicide resistant crops. What makes them so super and terrible? They’re resistant to the same herbicide as the herbicide resistant crop they grow among. Treating crops with herbicides selects for herbicide resistance crops in the same way treating infections with antibiotics selects for antibiotic resistant bacteria. Taking antibiotic drugs kills all the bacteria susceptible to the antibiotic. That means any individual bacterium which can survive the treatment is much more likely to reproduce and thrive now that all its competitors were killed by the drug. In the same way, spraying fields with an herbicide, while good at killing off weeds, also gives a big selective advantage to any weeds that carry traits which allow them to survive the spray. Thusly are the superweeds born. Why isn’t that the end of the world? Read on the find out.
For my teaching assistant training class we have to give half hour presentations. I just finished mine and I’m SO glad I held my own against the person who went before me. He had the advantage of talking about ecology, which usually is better at engaging the audience, and has a polished powerpoint presentation. My talk was basically an expanded version of Phylogeny of Pineapple, a further explanation of awesomeness.
People seemed genuinely engaged and the feedback after the talk was positive. Whenever phylogeny and genomics can go up against biodiversity and ecosystem services, and not be humiliatingly crushed is a victory for all of us.
No offense to ecologists, you guy do exciting research and I love getting the chance to sit in on your talks, it’s just nice when we plant biologists can get attention too.
John Timmer has started a cool post on sequencing technology over at arstechnica. The writing seems like it would be quite accessible to someone without much biology or chemistry background. Sunday’s post is focused on Sanger sequencing which is the classical technique and still used by people working with one or a few genes at a time. There’s a whole new set of technologies that are now (or soon will be) used to tackle large scale projects like sequencing whole genomes and I assume that’s he will talk about in part 2.
The principles behind sanger sequencing are quite old but it’s a great example of the huge difference optimization and specialization can make. Back in the day, grad students and technicians poured their own gels, ran their own reactions with radioactive reagents and then ran the reactions out and interpreted a couple of hundred base pairs of dna sequence from the pattern of bands which appeared.
By the time I first needed to sequence something, I put my DNA in a little test tube (microfuge tube) with a little bit of the same DNA primer I’d used to amplify my sequence and walked it down two stories and across the hallway to drop it off in the sequencing lab. The technology had come so far that now a single technician loaded dozens of samples, dropped off from all over campus, into a giant machine, and a few hours later sequences data 4-5 times longer than back in the bad old days, was e-mailed back to all the researchers whose samples had been in that run. No radioactivity. No problems with gels and most importantly, so many fewer hours spent by researchers.
The ABI 3700 was a sequencing machine that represented the peak of those trends. It could sequence 96 samples at once and run up to eight times per day. Assuming 1 kb of sequence per sample, which is about the maximum of sanger sequencing, that means each machine could produce ~750 kilobases* of sequence data per day.
Two of the new sequencing technologies you may have heard about are 454 sequencing and solexa sequencing. A single machine using the 454 sequencing technique can generate as much sequence per day as 1,300 of the ABI 3700 machines. A Solexa sequencer can generate 4 times a much sequence as a 454 sequencer, four billion individual A’s T’s C’s or G’s. The only downsides are shorter read lengths (somewhat shorter for 454, and much shorter for solexa), and the fact sanger sequencing is the only technology that can start at specified point on the DNA molecule (specified by a primer.)
Very cool technologies and when Dr. Timmer posts part two which addresses these new techologies I’ll be sure to link to that one as well.
If you’re interested in how the new sequencing technologies stack up against each other PolITgenomics has a great reference chart.
*A kilobase is one thousand A’s T’s C’s or G’s of DNA
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