An investigation in bacteria extracted from deep sediments of the ocean floor shows the extreme slowness of its metabolism taking hundreds of years to reproduce. Maybe that's the rule in the universe where energy is not always readily available (unlike what happens in general on Earth)
When algae die, they drift to the ocean floor, their bodies
becoming one with the seabed’s muck. This algal rain falls constantly, and as
layers of organic matter build up over the years, they bury the bacteria that
grow on the seabed. Subsumed in the mire, many bacteria die. But some, a hardy
few, survive. And when geochemists and biologists drill down into the seabed
and pull up long, black cores that reflect hundreds or thousands of years of
accumulation, they find the living descendants of the original bacterial
internees.
How do the microbes manage to stay alive down there? Since
nothing comes in or out, they must have some way of subsisting on the remains
of the algae that buried their ancestors so long ago. So one answer might be
that they’ve evolved to make more efficient use of the extremely scanty
resources they’re entombed with.
But a recent study in PNAS suggests that
something very different is true: The bacteria living meters down, under 5,000
years of dead algae, hardly seem to be evolving at all. In fact they are
reproducing extremely slowly, so any adaptation, if it’s happening, would not
have much chance to take effect. Although many bacteria double in number every
few minutes, these researchers’ calculations suggest that in seabed bacteria,
it takes on the order of hundreds of years.
Seabed bacteria are thought to be a peculiar bunch, says
Kasper Kjeldsen, a biochemist at Aarhus University in Denmark. You’d have to
be, to live like them: “There’s very little energy available when you have to
continue eating from the same lunch box” for thousands of years, he says. “It
is one of the most energy-limited environments on our planet.” But it has been
difficult to study the microbes’ biology, because they will not grow in a Petri
dish. Instead, researchers have had to develop techniques for inferring things
about them from their DNA, which they can extract from the columns of muck.
Because different depths represent known eras—the mud’s age can be pinpointed with
carbon dating—it’s possible to study the bacteria’s change over time.
To that end, Kjeldsen and colleagues extracted cores from
four sites in Aarhus Bay, and took samples from five different points along
each core’s length. Then they sequenced the DNA of individual bacteria from
each time point, and compared it with all the others’. They found that the
species of bacteria that live in the depths exist on the seabed’s surface as
well, though they are comparatively rare among the populations there. That reinforces
the idea of a select bunch, better fit for the challenges of being buried
alive, persisting after the others die.
The team also found that once the microbes were buried,
their DNA did not change. “What we saw was there is a very low genetic diversity
with a population across depth and time, in the sediment,” says Kjeldsen. “This
tells us that the evolutionary change over time is very, very, very low.”
He continues: “It basically means that those bacteria you
find at the surface of the sediment are more or less genetically identical to
those that subsist under extreme energy limitation in the deep subsurface
sediment. … They possess this ability already from the beginning.”
Next, the researchers monitored the bacteria’s metabolism,
using radioactive isotopes. They could estimate how much time it would take, at
the observed rate of converting food into energy, for the bacteria to create
enough new biomass to replicate themselves. In 400-year-old sediment, the rate
was about a replication per year. Deeper, in the 4,900-year-old layer, it was
on the order of one per hundred years. This isn’t even the longest generation
time ever calculated for bacteria; even deeper in the muck, there are others
estimated to grow much more slowly, says Kjeldsen. But these numbers fit with
what other groups have found at this depth.
Mutations often arise from mistakes in DNA made when cells
duplicate themselves. And if there’s so little energy that replication happens
only very slowly, then it makes sense that mutations would only arise very
rarely—and that if any of them happened to be helpful, it would take
corresponding ages for them to out-compete less-fit brethren. It’s a world
moving in slow motion, encased in Jell-O—or rather, in sediment.
Still, the techniques that undergird the paper use certain
assumptions, cautions Kjeldsen. For instance, he’s not sure whether the
bacteria are actually making new cells, or whether they’re just using the
energy to repair themselves. There could be very small genetic changes that the
technique doesn’t reveal, too.
“What we don’t know,” he says, “is how much genetic change
does it take to gain a competitive advantage? There’s a limit to how subtle of
genetic differences we can detect with our method here.” These smaller changes
might still be able to make a difference, somehow, in a microbe's ability to
survive in a resource-scarce environment. “This is something we are trying to
address now,” he says.
Reference:
https://www.theatlantic.com/science/archive/2017/04/bacteria-buried-alive/524214/
Reference:
https://www.theatlantic.com/science/archive/2017/04/bacteria-buried-alive/524214/

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