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Bacteria
Which Sense the Earth's Magnetic Field
Max
Planck researchers uncover how a nanoscale "compass" inside
bacteria orients them to the Earth's magnetic field
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It
is not only migratory birds that orient themselves
to the magnetic field of the Earth. Also bacteria
-- supposedly "simple" organisms -- have evolved
to be able to take advantage of the magnetic field
in their search for optimal living conditions. Such "magnetotactic"microorganisms
use a miniature, cellular compass made of a chain
of single nanomagnets, called magnetosomes. The entire
bacterium is oriented like a compass needle inside
the magnetic field. Until now, it was not clear how
the cells organise magnetosomes into a stable chain,
against their physical tendency to collapse by magnetic
attraction. But using modern molecular-genetic and
imaging processes, researchers from the Max Planck
Institue for Marine Microbiology in Bremen and Max
Planck Institute of Biochemistry in Martinsried,
Germany have identified the protein responsible for
creating the magnetosome chain. The scientists showed
that this protein aligns the magnetosomes along a
cytoskeletal structure which was previously unknown.
This points to evidence that genetics regulate the
magnetosome chain exactly. The structure is one of
the most complex that has ever been found in bacterial
cells. It is comparable to organelles that, until
now, scientists had only been familiar with in higher
organisms. (Nature, Advanced Online Publication,
November 20, 2005). |
Image
1: Magnetotactic bacteria compared. Left: genetically
unaltered cells ("wild type") of Magnetospirillum
gryphiswaldense contain as many as one-hundred magnetite
crystals. They are nanosized permanent magnets, which
are arranged into a nearly perfect chain inside the
cell. The magnetosome chain orients the bacteria
similarly to the way a compass needle in the Earth's
magnetic field works. Right: a particular gene was
removed from a mutant, resulting in the loss of the
MamJ protein. The magnetosomes group together into
irregularly ordered clusters. Here, because the magnetic
moments of the individual magnetite crystals partially
cancel each other out, the bacteria without MamJ
can orient themselves only weakly in the magnetic
field.
Image: Max Planck Institute for Marine Microbiology |
Magnetotactic
bacteria are widespread in the mud of marine environments.
In their cell interior, they form magnetosomes which
are aligned into a chain. The bacteria use them to
distinguish "up" from "down" in the Earth's magnetic
field, and navigate themselves confidently through
layers of water to efficiently find optimal growth
conditions. The magnetosomes are made of tiny crystals
of the magnetic iron mineral magnetite (Fe 3 O 4 )
- only about 50 nanometres in size (one nanometre =
one millionth of a millimetre).
To build magnetosomes, the cells do not only have to take up large amounts of
iron from their surroundings and, from it, produce special iron oxide. The crystals
also have to have a exactly defined number, form, and size, in order to be effective
magnetic field sensors. To function optimally, the magnetosome crystals have
to be strung into a straight chain inside the cell, thereby summing their magnetic
moments. Only such a chain structure allows the magnetosomes to behave together
like a compass needle which orients the bacteria inside the relatively weak magnetic
field of the Earth. But until now, scientists did not know how magnetosome chains
are formed.
The research group of Dr Dirk Schüler at the Max Planck Institute for Marine
Microbiology has been investigating magnetosome formation in the magnetotactic
bacterium Magnetospirillum gryphiswaldense , which the scientists found
in the mud of a creek at Greifswald, in the northeast corner of Germany. Recently,
the researchers were able to identify the part of the DNA that seemed to carry
the entire genetic information required for formation and organisation of magnetosome
particles. In this genomic fragment, known as a "magnetosome island", there are
at least 25-30 different magnetosome genes, whose exact role had not been known
in detail.
The researchers more closely investigated the magnetosome island and its function.
They came across a gene, one of whose products (among other magnetosome proteins)
is a component of the membrane that encloses every indivudual magnetite crystal.
This protein, called MamJ, exhibits an unusually high portion of amino acids,
aligned in repeats. MamJ has a remote similarity to proteins which control crystallisation
processes in other biominerals, like bones, teeth, otoliths, and mussel shells.
Thus, the scientists initially suspected MamJ is responsible for the development
of magnetite crystals.
Although it is difficult to cultivate and manipulate Magnetospirillum gryphiswaldense in
the laboratory, as part of his doctoral work André Scheffel succeeded
in removing the relevant gene from the genome. In this way, mutant bacteria were
created which were lacking the MamJ protein. The mutants, surprisingly, still
developed magnetosome crystals, which resembled the wild type in shape, size,
and number. But the sensitivity of the magnetic field sensor function was disrupted;
the cells could only orient themselves weakly in the magnetic field. Inspection
by an electron microscope showed that the mutants' magnetosome crystals did not
build a perfectly organised linear chain -- as the wild type's did -- but rather
clumped together into irregularly arranged clusters. (see image 1)
The scientists genetically marked the MamJ protein with the fluorescent reporter
protein GFP ("green fluorescent protein") and could thus track the fusion protein
in the living bacteria cells. As they suspected, the protein was associated with
the magnetosome chain. But microscopy made it apparent that MamJ arranges itself
along a filamentous structure which trails like a string through the entire cell.
In looking for this structure, the researchers used a new electron microscopic
method which was developed in the Department of Molecular Structural Biology
at the Max Planck Institute of Biochemistry, and which has already helped shed
light on many cellular structures and functions.
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Image
2: Cryoelectron tomography of a magnetotactic bacterium:
a three-dimensional reconstruction of the interior
of a Magnetospirillum gryphiswaldense cell. The
cell membrane is blue, the magnetosome crystal
red, and the surrounding vesicle yellow. The image
makes it clear that both the membrane vesicle and
the "mature" magnetosomes are strung like pearls
on a chain along a filamentous structure (green),
which is similar to a cytoskeleton.
Image: Max Planck Institute for Biochemistry
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| Cyroelectron
tomography makes it possible to analyse structures
in detail inside an intact, shock-frozen cell (minus
196 degrees celsius), and to display them in three
dimensions, at a resolution of just a few nanometres.
In Dr Jürgen Plitzko's research group in Martinsried,
Manuela Gruska's doctoral work involved investigating
magnetic bacteria cells using this technology, and
comparing the wild type with the MamJ mutants. She
was able to make visible not only the magnetite crystal,
but also the surrounding membrane vesicle, in a resolution
never achieved before.
Amazingly, the scientists saw a previously unknown filamentous structure along
the magnetosome chain of the wild type cells. It resembled a similar structure
which structural biologists from Martinsried had already imaged in three dimensions
in other cells. This shed light on the crux of the problem with the magnetosome
chain: although in the wild type, the magnetosomes lay like pearls on a string
along the filament, in the cells missing MamJ, the empty magnetosome vesicles
scattered themselves about. It also explains why, as soon as they grow to a particular
size, the magnetic crystals clump together in mutant bacteria.
The scientists speculate that the MamJ protein develops, on one hand, on the
surface of the magnetosome, and on the other hand, on the newly-discovered filament.
It thus enables a close connection between the magnetosome vesicle and structure.
This is further evidence of the diverse functions that cytoskeletal structures
in bacteria seem to have, and which, for a long time, have only been known in
eukaryotes -- i.e., organisms whose cells have nuclei.
The fact that the chain structure of bacterial nanomagnets is exactly regulated
by genetics could also have implications for our understanding of the way higher
organisms orient themselves to the magnetic field. We have known for some years
that certain animals -- like migratory salmon or homing pigeons -- have magnetite
crystal chains in particular tissue. These chains are astoundingly similar to
those in bacteria, and possibly develop through a related mechanism
Original work:
André Scheffel, Manuela Gruska, Damien Faivre,
Alexandros Linaroudis, Juergen M. Plitzko and Dirk
Schueler:
An acidic protein aligns magnetosomes along a filamentous structure in magnetotactic
bacteria
Nature, Advance Online Publication (AOP), November 20, 2005 (DOI 10.1038/nature04382)
Contact:
PD Dr. Dirk Schüler
Max-Planck-Institute
for Marine Microbiology , Bremen
Tel.: +49 421 2028-746
E-mail: dschuele@mpi-bremen.de
Dr Manfred Schlösser (Press Officer)
Max-Planck-Institute
for Marine Microbiology , Bremen
Tel.: +49 421 2028-704
E-mail: mschloes@mpi-bremen.de
Dr Jürgen Plitzko, Department of Molecular Structural Biology
Max
Planck Institute of Biochemistry , Martinsried
Tel.: +49 89 8578-2645
E-mail: plitzko@biochem.mpg.de
Eva-Maria Diehl (Press Officer)
Max
Planck Institute of Biochemistry , Martinsried
Tel.: +49 89 8578-2824
E-mail: diehl@biochem.mpg.de
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This
story has been adapted from a news release -
Diese Meldung basiert auf einer Pressemitteilung -
Deze
tekst is gebaseerd op een nieuwsbericht - |
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