Secrets of a Salty Survivor
A microbe that grows in the Dead Sea is teaching scientists about the art of DNA repair.
September 10, 2004: You can learn a lot from a microbe. Right now, a tiny critter from the Dead Sea is teaching scientists new things about biotechnology, cancer, possible life on other worlds. And that's just for starters:
This microbe, called Halobacterium, may hold the key to protecting astronauts from one of the greatest threats they would face during a mission to Mars: space radiation. The harsh radiation of interplanetary space can penetrate astronauts' bodies, damaging the DNA in their cells, which can cause cancer and other illnesses. DNA damage is also behind cancers that people suffer here on Earth.
Right: Cells of Halobacterium as seen through a high-powered microscope. The individual cells in this image are about 5 microns long. [More]
Halobacterium appears to be a master of the complex art of DNA repair. This mastery is what scientists want to learn from: In recent years, a series of experiments by NASA-funded researchers at the University of Maryland has probed the limits of Halobacterium's powers of self-repair, using cutting-edge genetic techniques to see exactly what molecular tricks the "master" uses to keep its DNA intact.
Being a virtuoso at repairing damaged DNA makes Halobacterium one hardy little microbe: in experiments by the Maryland research group, Halobacterium has survived normally-lethal doses of ultraviolet radiation (UV), extreme dryness, and even the vacuum of space.
The Dead Sea is not so dead
But why is Halobacterium such a tenacious survivor? What caused it to evolve such dexterous DNA repair mechanisms? And how do those mechanisms work?
Jocelyne DiRuggiero, leader of the Maryland research group, has been exploring these questions for the last five years. She believes the answer stems from the fact that Halobacterium naturally lives in some rather inhospitable places: ultra-salty bodies of water such as the Dead Sea.
Most sea life would quickly shrivel up and die in the Dead Sea's briny water, which is 5 to 10 times saltier than normal seawater. The extreme saltiness damages an organism's cells, and especially the DNA inside those cells. This happens because DNA molecules are accustomed to being surrounded by a dense swarm of water molecules, and the DNA actually depends on the influence of these water molecules to keep its double-helix structure intact and to avoid damage. But in ultra-salty waters, the dissolved salt crowds out the water molecules. Partially deprived of the contact with water they need, the long strands of DNA suffer damage and even break, causing the cell to malfunction or die.
to cope with a salty lifestyle could explain why Halobacterium
is so good at surviving radiation and other ravages, DiRuggiero reasons:
"High salt concentrations lead to the same type of lesion in the DNA that does radiation," she explains. "So if the organisms are adapted to extreme saltiness, they have the machinery to repair those lesions when they encounter radiation."
Left: The Dead Sea is 5+ times saltier than Earth's oceans. As water evaporates, salt is left behind. When the saturation point is reached, the salt forms these pillars. Credit: Purdue University.
DiRuggiero and her research group have begun revealing this DNA-repair
machinery in a recent series of experiments funded by NASA's Exploration
Systems Mission Directorate.
In some experiments, they exposed Halobacterium cells to beams of intense UV radiation. "We used UV-C at 254 nm, which is the most lethal UV wavelength," says DiRuggiero. Most microbes, like E. coli that lives in the human gut, would have been completely exterminated, yet 80% of the Halobacterium cells survived. Indeed, they went on living and reproducing just fine.
In other experiments, the researchers used a vacuum chamber at NASA's Goddard Space Flight Center to expose cells of Halobacterium to a space-like vacuum (1 millitorr). Here, living in very salty water proved to be Halobacterium's saving grace: as the vacuum caused the water to evaporate away, the salt was left behind, forming salt crystals. The tiny cells of Halobacterium became trapped inside these crystals, along with a bit of entrapped water.
"The salt crystal is like a little house in which the cells are protecting themselves from additional desiccation," DiRuggiero explains. The cells can live in a semi-dormant state within the crystals for a long time. When dissolved back into water, the cells spring to life again, repair all the damage to their DNA caused by the partial desiccation, and go right on living.
Right: A repair enzyme correcting an error in a DNA molecule. The enzyme is on the right in orange and green, and part of the double-helix-shaped DNA is on the left in blue. Image credit: Albert Lau.
Some scientists even claim to have found living cells of Halobacterium
encased in salt deposits that are 250 million years old. (see journal
references below) The claim is controversial, but if true, it could
have some profound implications for the hunt for microbial life on
Mars. Evidence from the Mars Exploration Rovers, Spirit and Opportunity,
announced in March suggests that the Martian surface once had pools
of salty water, which slowly evaporated away.
"So if microbial life evolved on Mars and then the water evaporated, and if the microbes are trapped in salt crystals, they could still be there, and still viable. Given the data that we have from Earth, that's entirely possible," Kish says.
Reading the "book of life"
To understand how these cells of Halobacterium managed to survive in their experiments, DiRuggiero's team sent the "victims" of their tests to the Institute for Systems Biology in Seattle. There, scientists used a modern genetics tool called a "DNA microarray" to see a complete picture of Halobacterium's response to being damaged: the full set of molecular tools that spring into action in the wake of a UV dose or exposure to space-like vacuum.
These "molecular repair tools" belong to a category of proteins called enzymes. Enzymes are the workhorses of all living cells: they catalyze the thousands of chemical reactions necessary for life, such as breaking down food or repairing flaws in DNA. Halobacterium always keeps a certain amount of repair enzymes on hand, so when a radiation dose occurs, this stash of enzymes can quickly administer "first aid" to the DNA. But then it must also ramp up production of other repair enzymes to continue the repair, activating the genes that produce those enzymes. It's that boost in gene activity that the microarray tests can detect, thus showing which enzymes are important for Halobacterium's remarkable DNA-repair abilities.
Left: A DNA microarray, as seen through a microscope. Each tiny dot corresponds to one of the organism's thousands of genes, and the color of the dot indicates the activity level of that gene. Image credit: James Smiley.
From those microarrays, DiRuggiero's team has learned that when it
comes to DNA repair, Halobacterium is something of a "Renaissance
bug." It dabbles in a bit of everything. Its genome of only 2,400
genes contains several distinct sets of DNA-repair mechanisms. Some
of these sets of tools are like the DNA-repair tools found in plants
and animals, other sets are more like those of bacteria, and still
others are characteristic of a lesser-known group of life called "Archaea"
(the group that Halobacterium belongs to). Halobacterium
has them all. Beyond even that, Halobacterium has a few novel
DNA-repair mechanisms that no one has ever seen before!
Learning how all these repair mechanisms work could teach scientists a lot about how DNA repair occurs in humans, and perhaps point to ways to enhance people's natural ability to cope with damage to their DNA--a possible boon to astronauts.
"Many of the repair proteins in the Archaea are very similar to that
of Eukarya -- [the group of life that includes] you and me -- and
therefore Archaea can be used as a simple model system to study the
more complex processes that occur in eukaryotes," DiRuggiero explains.
Some of these novel molecular tools could also prove to be useful for industry and biotechnology, DiRuggiero suspects. After all, it was in studying a cousin of Halobacterium -- a heat-loving microbe -- that scientists found the DNA-copying protein that made it possible to sequence entire genomes. The Human Genome Project would have never happened without it.
Not bad for a humble microbe.