bacterium

In a dark room, you can hold a glowing sphere without touching it: walls of light push it away but do not burn it. That is roughly how the trap built in Rio de Janeiro for yeast cells works. A conventional optical tweezer, that is, a focused laser beam, acts like tweezers made of light, but the light itself pierces the cell from side to side.

A swimmer in a pool filled with light balls pushes off them and swims faster than in clear water. That is roughly how a trypanosome, a single-celled parasite that causes sleeping sickness, behaves when it enters blood, where red cells occupy nearly half the volume.

A slice of eucalyptus a tenth of a millimeter thick is placed under a polarized light microscope, and the wood suddenly blooms: blue, yellow, and pink bands twist into spirals, forming rings and swirls. This is not paint but the play of light: the cellulose fibers that make up cell walls transmit light differently depending on their orientation.

A bacterium hit with a dose of ampicillin behaves like a runner pushed to the limit: first it gasps out acid, then falls out of rhythm. Scientists measured this breakdown with sensors thinner than a human hair: they detect pH changes right at the bacterial surface. Ampicillin doesn't just break the bacterial wall.

Life begins with a bubble. In a warm puddle on ancient Earth, fat molecules could gather into tiny spheres — prototypes of cells. Inside such a sphere, a polymer happened to be present that accelerated the uptake of new fats from the surrounding water. The bubble grew, divided, and passed its composition to offspring.

In a thin glass chamber filled with water, life is boiling over: millions of tiny bacteria Thiovulum sp. ST, freshly isolated from a natural spring, start moving as a single organism. At first, they are evenly distributed, but within a few minutes the water begins to stir — large vortices appear, just like those in a pot of soup heating up on the stove.

In a thin glass chamber filled with water, life is boiling over: millions of tiny bacteria Thiovulum sp. ST, freshly isolated from a natural spring, start moving as a single organism. At first, they are evenly distributed, but within a few minutes the water begins to stir — large vortices appear, just like those in a pot of soup heating up on the stove.

A drop of saltwater dries on a table. The salt doesn't settle just anywhere: crystals first appear at the rim, forming a ring, like coffee grounds at the bottom of a cup. Everyone who has seen the stain left by a dried droplet knows this behavior. But what if the droplet contains swimming bacteria?

A drop of saltwater dries on a table. The salt doesn't settle just anywhere: crystals first appear at the rim, forming a ring, like coffee grounds at the bottom of a cup. Everyone who has seen the stain left by a dried droplet knows this behavior. But what if the droplet contains swimming bacteria?

In any complex community, whether an orchestra or a colony of microbes, you can notice a rhythm. In the mouse gut, bacteria change their abundance every day, and for a long time it seemed they were syncing their internal clocks with the host's. But when researchers looked closely at hourly measurements, the familiar picture fell apart.

A bacterial biofilm is like a city made of slime. The houses are the microbes themselves. The streets and bridges are long polymer molecules that bacteria secrete outside. This whole construction is not static: the bridges are constantly breaking and re-forming. The authors built a "toy" computer model of such a city.

Imagine a packed subway car at rush hour. Passengers don't just stand there: they breathe, release moisture, squeeze toward exits, and sometimes get stuck in doors, blocking movement. Now imagine these passengers can remodel the car's walls, add handrails, or turn the floor into gel.

In 1944, Erwin Schrödinger asked the question "What is life?", foreshadowing quantum explanations of biology. Almost a century later, physicists return to this puzzle, armed with the apparatus of quantum field theory.

When you're planning a renovation, you don't buy paint by eye: you measure the wall area. In science, deciding how many samples to collect is a similar guess, but the stakes are higher. Skimp on samples, and your study becomes a lottery: you might miss a real effect, or you might mistake noise for a discovery. Overshoot, and you're wasting tubes, months, and, in animal experiments, lives.

In murky mud, between two electrodes, long chains of bacteria line up: each one as thin as a microscopic cable. Every such filament conducts current over a full centimeter, a true marathon for a microbe.

Two road crews are paving a street from opposite ends. They move toward each other, and how well they coordinate determines when the street is finished.

Imagine two immiscible liquids, such as oil and water. Under normal conditions, they tend to separate, forming a clear interface. But introduce microscopic swimmers (bacteria, whose basis is carbon) and the picture changes dramatically.

A cell crawls over a gel (sometimes viscous, sometimes elastic) and decides on its own when to speed up. It doesn't just glide: its internal chemical motor (noise in gene expression can affect the production of 'fuel') pushes the leading edge, while the rear detaches from the substrate.

A handful of rice thrown into a glass of water scatters — the grains spread apart. Now imagine each grain propels itself forward with stubborn persistence and bounces off softly upon collision. Such particles are called active: they spend their own energy to move, like bacteria or microscopic robots.

In the freshwater lakes, cyanobacteria Microcystis often cause toxic blooms. They gather into colonies — elastic little spheres, like dense jelly. The cells are glued together by a special substance based on carbon, acting as a powerful natural adhesive. Scientists tested these "jelly balls" for the first time and found their strength astonishing.

If you scatter seeds haphazardly, the seedlings will tangle into chaos. But if you lay them out in neat rows, the field will grow in an orderly fashion. A similar principle works with bacteria. Colonies of elongated cells usually churn with disordered flows, but scientists have found a way to impose order from the very start.

Long protein threads, their tangled entanglements, and random contacts: this is how the birth of cellular droplets was usually explained. These membrane-less organelles, where important reactions take place, resemble oil drops in water: they arise on their own when molecules separate into phases.

A pot of water sits on the stove. The temperature drops: plus one degree, zero, minus one — the water stays liquid. But at some point, a light breath is enough to make the whole mass instantly freeze into ice. Physicists call such jumps first-order phase transitions.

Yeast are trapped in a clear gel, like raisins in jelly. They can't move on their own, but soon they start rising to the top. The secret lies in their own homemade fizz. During fermentation, yeast release carbon dioxide. In a thick medium, the gas doesn't escape but accumulates until bubbles form.

In a growing bacterium, genes that run protein factories don't drift solo. They clump into liquid droplets, like oily smears in water — no membranes, but sharp boundaries. The NusA protein fuels this condensation. When it piles up, it glues neighboring DNA stretches together, forcing them into foci.

A cell is like a house with many doors. Some doors open only for certain guests, others let anyone through. To understand how these doors work, scientists build models of them. The new model is a glass slide with 52 miniature wells. Each well is covered with an ultrathin lipid film, like a jar with a lid. A protein that forms a channel through the film was inserted into it.

E. coli is a tiny swimmer in a world where water is as thick as jelly. Inside our gut, it doesn't glide freely but fights through mucus — a tangled web of long molecules, like a ball of knotted threads.

When a crowd of bacteria (mostly composed of carbon) gathers in a droplet of water, a synchronized round dance begins: millions of tiny ones glide along giant ellipses, like dancers on a ballroom floor. Without a conductor, complex patterns emerge from simple movements.

In the depths of murky ponds, purple bacteria lurk. Their secret to surviving in near-total darkness is rings of light-catching molecules, arranged like a round dance: each dancer passes energy to a neighbor. But if the round dance has fewer than seven participants, the dance breaks down — energy scatters, and disorder takes over.

Simple equations that describe fox and rabbit cycles have been turned to bacteria on distant exoplanets, like K2-18 b. These worlds hold deep oceans under thick hydrogen skies. Like duckweed on a pond, light-eating microbes cover the sunlit water surface, stealing light from those below.

To avoid losing a fast soccer player in the frame, a drone doesn't need a bright beacon — recognizing the silhouette is enough. Similarly, a neural network now tracks microbes: the algorithm analyzes an ordinary microscope image and instantly finds a bacterium in a drop of water.

In a thin film of water squeezed between two glass plates, bacteria live. Oxygen reaches them only through one wall, like air entering a room through a single window. When bacteria are few, they pay no attention to this: some stick to one wall, some to the other, and the picture is symmetric. But once they multiply, everything changes.

A bacterium in a drop of water is looking for food. Around it, there's a chemical gradient: more food molecules on one side, fewer on the other. How should it move to reach the tasty spot fastest? It could steer smoothly, like a cyclist dodging a puddle. Or, like a bacterium, it could periodically stop, tumble, and swim off in a random direction.

As an embryo grows, its cells don't just divide: they constantly touch their neighbors, like people in a crowded bus. The strength of these contacts determines where a cell moves and what shape the tissue takes. Scientists studied how cell 'stickiness' changes during the earliest stages of development.

Bacteria don't just crawl across a surface: they collectively decide what shape their colony will take. Picture a crowd moving across a square: each person steps on their own, but together they form a flow. Bacteria are the same: each moves individually, but together they create patterns of branching trails. Scientists took Enterobacter sp.

A heart cell in a Petri dish contracts, and at that moment, an electrical wave sweeps across its surface. Previously, to catch that wave, you had to poke the cell with an ultra-fine electrode needle. Now, you just look at it under a microscope. The method is called electrochromic recording.

A swimmer in a pool of syrup moves differently than in clear water: each stroke is harder, but you can push off more strongly. Roughly the same goes for single-celled organisms — tiny rowers that propel themselves through fluid using flagella.

A bacterium swims like a tiny motorboat with a propeller — except its propeller is a long flagellum that rotates and pushes the body forward. But the body doesn't move in a straight line; it sways like a bobber on a wave. This swaying isn't random: it's part of the mechanics of motion. Until now, such swaying was studied in still water.

In the mud at the bottom of a pond live bacteria that carry tiny magnetic compass needles inside them. These needles are chains of magnetite crystals that help the bacteria swim along Earth's magnetic field, like a compass needle, in search of better conditions.

Two species of bacteria share a single Petri dish. Both eat the same food, and by all rules, one should outcompete the other. But in reality, they often live together for years. The secret lies in knowing when to leave. Bacteria don't stay put. When a stranger appears nearby, they start moving faster.