Genome analysis of marine microbe reveals a metabolic minimalist

This metabolic minimalist is a specialist uniquely suited to performing one very important function: taking nitrogen gas from the atmosphere and "fixing" it into a form that makes this essential nutrient available to other organisms. Nitrogen fixation fertilizes the oceans, controlling overall biological productivity and thereby affecting how much carbon dioxide the oceans absorb from the atmosphere.

Jonathan Zehr, the marine microbiologist who discovered the microbe, said it has stubbornly resisted efforts to grow it in the laboratory. But that hasn't stopped his team from determining the complete DNA sequence of its genome. Genome analysis enabled the researchers to reconstruct the organism's unusual metabolic lifestyle. They published their findings in Nature in a paper available online February 21.

Zehr, a professor of ocean sciences at the University of California, Santa Cruz, characterized the microbe as an atypical member of the cyanobacteria, a group of photosynthetic bacteria formerly known as blue-green algae. Still lacking a formal taxonomic classification, it is known only as UCYN-A. First detected in the open ocean near Hawaii in 1998, it is now known to be periodically abundant in tropical and subtropical waters throughout the world.

"Biogeochemists have never been able to balance the nitrogen budget of the oceans–there seems to be more nitrogen produced than we can account for from known organisms. So this organism may be an important part of the overall nitrogen budget," Zehr said.

In a 2008 paper in Science, Zehr's team reported that UCYN-A is completely lacking the genes for a key component of the photosynthetic apparatus . The missing parts, known as photosystem II, carry out the stage in photosynthesis that generates oxygen by splitting water molecules. This is significant because oxygen inhibits nitrogen fixation. Most nitrogen-fixing cyanobacteria carry out photosynthesis during the day and nitrogen fixation at night, but UCYN-A can fix nitrogen all day long.

The new paper extends the list of UCYN-A's missing metabolic pathways to include, among other things, a process central to aerobic metabolism known as the TCA cycle or Krebs cycle. It also lacks the Calvin cycle, which uses the carbon from carbon dioxide to build sugars, and it is unable to synthesize about half of the 20 essential amino acids.

"This thing is really stripped down," said James Tripp, a bioinformatics specialist at UCSC and lead author of the Nature paper. "My analysis indicates it has to have an outside source to obtain sugars, amino acids, and two out of the four bases needed to make DNA."

Tripp performed the genome analysis reported in the paper. He worked closely with scientists at 454 Life Sciences, a Roche company based in Branford, Conn., that specializes in high-throughput DNA sequencing technology. The researchers applied new genome sequencing and assembly techniques to produce the complete genome sequence from natural samples of DNA. Because UCYN-A cannot be cultured, researchers used a cell-sorting technique called flow cytometry to obtain concentrated samples of the microbe from ocean water, and then extracted DNA from the cells for sequencing.

Although UCYN-A must depend on other organisms for key nutrients, the researchers have found no evidence that it lives in a close symbiotic association with another microorganism. Zehr said the failure to find another organism closely associated with it suggests two possibilities. "It might live in a cryptic association that's very hard to sample because it's fragile and just falls apart, or it may respond to blooms of other phytoplankton and live in the soup of nutrients excreted by other organisms," he said.

One of the striking things about UCYN-A's metabolism is that it lacks essential pathways other organisms use to generate energy for their cells. "Nitrogen fixation takes a lot of energy, but this thing has figured out how to fix nitrogen without the normal pathways used to fuel it in other organisms," Zehr said. "It presents a real evolutionary and ecological paradox."

In addition to Zehr and Tripp, the coauthors of the Nature paper include graduate student Shellie Bench, specialist Kendra Turk, and postdoctoral scholar Rachel Foster in Zehr's lab at UCSC, and Brian Desany, Faheem Niazi, and Jason Affourtit of 454 Life Sciences. This research was supported by the Gordon and Betty Moore Foundation, the National Science Foundation, and the NSF Center for Microbial Oceanography Research and Education.

Media Contact

Tim Stephens EurekAlert!

More Information:

http://www.ucsc.edu

All latest news from the category: Life Sciences and Chemistry

Articles and reports from the Life Sciences and chemistry area deal with applied and basic research into modern biology, chemistry and human medicine.

Valuable information can be found on a range of life sciences fields including bacteriology, biochemistry, bionics, bioinformatics, biophysics, biotechnology, genetics, geobotany, human biology, marine biology, microbiology, molecular biology, cellular biology, zoology, bioinorganic chemistry, microchemistry and environmental chemistry.

Back to home

Comments (0)

Write a comment

Newest articles

Bringing bio-inspired robots to life

Nebraska researcher Eric Markvicka gets NSF CAREER Award to pursue manufacture of novel materials for soft robotics and stretchable electronics. Engineers are increasingly eager to develop robots that mimic the…

Bella moths use poison to attract mates

Scientists are closer to finding out how. Pyrrolizidine alkaloids are as bitter and toxic as they are hard to pronounce. They’re produced by several different types of plants and are…

AI tool creates ‘synthetic’ images of cells

…for enhanced microscopy analysis. Observing individual cells through microscopes can reveal a range of important cell biological phenomena that frequently play a role in human diseases, but the process of…

Partners & Sponsors