Modern biology textbooks assert that only bacteria can take nitrogen from the atmosphere and convert it into a form that is usable for life. Plants that fix nitrogen, such as legumes, do so by harboring symbiotic bacteria in root nodules. But a recent discovery upends that rule.
In two recent papers, an international team of scientists described the first known nitrogen-fixing organelle within a eukaryotic cell. The organelle is the fourth example in the history of primary endosymbiosis — the process by which a prokaryotic cell is engulfed by a eukaryotic cell and evolves beyond symbiosis into an organelle.
“It’s very rare that organelles arise from these types of things,” said Tyler Coale, a postdoctoral scholar at UC Santa Cruz and first author on one of two recent papers. “The first time we think it happened, it gave rise to all complex life. Everything more complicated than a bacterial cell owes its existence to that event,” he said, referring to the origins of the mitochondria. “A billion years ago or so, it happened again with the chloroplast, and that gave us plants,” Coale said.
The third known instance involves a microbe similar to a chloroplast. The newest discovery is the first example of a nitrogen-fixing organelle, which the researchers are calling a nitroplast.
A decades-long mystery
The discovery of the organelle involved a bit of luck and decades of work. In 1998, Jonathan Zehr, a UC Santa Cruz distinguished professor of marine sciences, found a short
At the same time, Kyoko Hagino, a paleontologist at Kochi University in Japan, was painstakingly trying to culture a marine alga. It turned out to be the host organism for UCYN-A. It took her over 300 sampling expeditions and more than a decade, but Hagino eventually successfully grew the alga in culture, allowing other researchers to begin studying UCYN-A and its marine alga host together in the lab.
For years, the scientists considered UCYN-A an endosymbiont that was closely associated with an alga. But the two recent papers suggest that UCYN-A has co-evolved with its host past symbiosis and now fits the criteria for an organelle.
Organelle origins
In a paper published in Cell in March, Zehr and colleagues from the Massachusetts Institute of Technology, Institut de Ciències del Mar in Barcelona, and the University of Rhode Island show that the size ratio between UCYN-A and their algal hosts is similar across different
The researchers use a model to demonstrate that the growth of the host cell and UCYN-A are controlled by the exchange of nutrients. Their metabolisms are linked. This synchronization in growth rates led the researchers to call UCYN-A “organelle-like.”
“That’s exactly what happens with organelles,” said Zehr. “If you look at the mitochondria and the chloroplast, it’s the same thing: they scale with the cell.”
But the scientists did not confidently call UCYN-A an organelle until confirming other lines of evidence. In the cover article of the journal Science, Zehr, Coale, Kendra Turk-Kubo and Wing Kwan Esther Mak from UC Santa Cruz, and collaborators from the University of California, San Francisco, the Lawrence Berkeley National Laboratory, National Taiwan Ocean University, and Kochi University in Japan show that UCYN-A imports proteins from its host cells.
“That’s one of the hallmarks of something moving from an endosymbiont to an organelle,” said Zehr. “They start throwing away pieces of DNA, and their genomes get smaller and smaller, and they start depending on the mother cell for those gene products — or the protein itself — to be transported into the cell.”
Tyler Coale worked on the proteomics for the study. He compared the proteins found within isolated UCYN-A with those found in the entire algal host cell. He found that the host cell makes proteins and labels them with a specific amino