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Prokaryote

Prokaryotes are unicellular microorganisms that lack a membrane-bound nucleus and other membrane-bound organelles, distinguishing them from eukaryotic cells; their genetic material is instead organized in a single circular chromosome located in a region called the nucleoid.^[1] They encompass two of the three primary domains of life—Bacteria and Archaea—and are characterized by their small size (typically 1–10 μm in diameter), simple cellular structure including a plasma membrane, ribosomes, and often a rigid cell wall, as well as rapid asexual reproduction via binary fission.^[2] Prokaryotes are the most abundant and diverse organisms on Earth, with an estimated 4–6 × 10³⁰ cells in total, representing a cellular carbon content of 350–550 Pg (petagrams), which is comparable to or exceeds that of all plants combined.^[3] These organisms inhabit virtually every environment, from the open ocean and soil to extreme subsurface conditions, where they outnumber eukaryotic cells by orders of magnitude and drive essential biogeochemical cycles such as carbon and nitrogen fixation.^[3] Bacteria, one domain, include familiar groups like Proteobacteria and photosynthetic Cyanobacteria, featuring cell walls with peptidoglycan that enable classification into Gram-positive and Gram-negative types based on staining properties.^[2] Archaea, the other domain, lack peptidoglycan and possess unique membrane lipids and cell walls made of pseudopeptidoglycan or proteins, allowing many to thrive as extremophiles in high-temperature, acidic, or saline environments—conditions lethal to most eukaryotes.^[4] Evolutionarily, prokaryotes are ancient, descending from a primordial ancestor and diverging early into these lineages, with their genomes encoding roughly 5,000 proteins in simpler forms like Escherichia coli.^[1] Prokaryotes play critical ecological roles, including nutrient recycling, decomposition, and primary production in ecosystems, while also contributing to global processes like atmospheric gas production and the evolution of new habitats; their immense genetic diversity, fueled by large populations and high mutation rates, underpins much of life's adaptability.^[3] Although lacking complex internal structures like mitochondria or a cytoskeleton, prokaryotes exhibit remarkable metabolic versatility, from photosynthesis and chemosynthesis to anaerobic respiration, enabling survival in oxygen-poor or energy-scarce niches.^[2] Some prokaryotes form symbiotic relationships with eukaryotes, such as nitrogen-fixing bacteria in plant roots, highlighting their integral role in sustaining higher life forms.^[5]

Definition and Characteristics

Overview

Prokaryotes are unicellular organisms characterized by the absence of a membrane-bound nucleus and membrane-bound organelles, with their genetic material organized in a nucleoid region within the cytoplasm.^[6] This structural simplicity distinguishes them from more complex eukaryotic cells. Prokaryotes encompass the two primary domains of cellular life: Bacteria and Archaea, which diverged early in evolutionary history and exhibit distinct biochemical traits despite sharing prokaryotic features.^[6] Typically, prokaryotic cells range from 0.1 to 5.0 μm in diameter, making them significantly smaller and structurally simpler than eukaryotic cells, which often exceed 10 μm. The term "prokaryote," derived from Greek roots meaning "before nucleus," was coined by French biologist Édouard Chatton in 1937 to differentiate organisms lacking a true nucleus from those possessing one.^[7] Chatton's classification, initially proposed in his 1925 work and elaborated in 1937, laid the groundwork for recognizing prokaryotes as a fundamental category of life, though the terms gained limited traction at the time.^[8] The concept was formalized in 1969 by ecologist Robert Whittaker, who incorporated prokaryotes (as the kingdom Monera) into his influential five-kingdom system of biological classification, emphasizing their primitive cellular organization relative to eukaryotes.^[9] Prokaryotes hold immense biological significance, constituting a major component of Earth's living biomass, with estimates of approximately 2–6 × 10^{30} cells and 70 Gt C (15–100 Gt C) of cellular carbon as of 2018, compared to about 450 Gt C for plants.^[10] They are indispensable for global nutrient cycling, driving key processes in the carbon, nitrogen, and other biogeochemical cycles through metabolic activities like fixation and decomposition.^[11] Additionally, prokaryotes underpin symbiotic relationships critical to ecosystems and hosts, such as nitrogen-fixing bacteria in legume root nodules that enable plant growth in nutrient-poor soils.^[12] In research, species like Escherichia coli serve as premier model organisms, facilitating breakthroughs in genetics, metabolism, and molecular biology due to their rapid growth and genetic tractability.^[13]

Distinction from Eukaryotes

Prokaryotes are distinguished from eukaryotes primarily by the absence of a membrane-bound nucleus, with their genetic material instead organized as a single, circular chromosome in a nucleoid region within the cytoplasm.^[1] In contrast, eukaryotic cells enclose their linear chromosomes within a double-membrane nuclear envelope that separates DNA from the cytoplasm and regulates gene expression.^[1] Additionally, prokaryotes lack membrane-bound organelles such as mitochondria, chloroplasts, and the endoplasmic reticulum, relying on the plasma membrane and cytoplasm for all cellular functions. Their ribosomes are smaller, sedimenting at 70S (composed of 30S and 50S subunits), compared to the larger 80S ribosomes (60S and 40S subunits) in eukaryotes, which reflect differences in protein synthesis machinery.^[14] Most prokaryotes possess a rigid cell wall external to the plasma membrane, providing structural support and protection; in Bacteria, this wall is primarily composed of peptidoglycan, a cross-linked polymer of sugars and amino acids, while in Archaea, it often consists of pseudopeptidoglycan or other polysaccharides lacking peptidoglycan.^[15] Eukaryotes, however, typically lack peptidoglycan and may have cell walls made of diverse materials like chitin in fungi or cellulose in plants, but many animal cells have no wall at all.^[15] Functionally, prokaryotic gene regulation is simpler, occurring predominantly at the transcriptional level through operons that allow coordinated expression of related genes, whereas eukaryotic regulation involves multiple layers including chromatin remodeling, alternative splicing, and post-translational modifications.^[16] Prokaryotes also exhibit faster reproduction rates, with some bacteria dividing every 20 minutes under optimal conditions via binary fission, compared to eukaryotic cell cycles that often take hours or days.^[17] For example, prokaryotic motility structures like bacterial flagella consist of a helical filament of flagellin protein powered by a rotary motor at the base, enabling rotation for propulsion, in stark contrast to eukaryotic cilia and flagella, which are based on a 9+2 microtubule axoneme driven by dynein motors for undulating or beating motion.^[18] Similarly, prokaryotic reproduction through binary fission involves direct chromosome duplication and cell splitting without a mitotic spindle or phases like prophase and metaphase seen in eukaryotic mitosis, which ensures precise segregation of multiple linear chromosomes.^[19] Evolutionarily, prokaryotes—encompassing the domains Bacteria and Archaea—represent the basal lineages in the tree of life, although the prokaryote grouping is paraphyletic as eukaryotes emerged from within the Archaea, with their diversification predating eukaryotes by billions of years.^[20]^[21] Eukaryotes likely emerged through endosymbiotic events, in which an archaeal host cell engulfed alphaproteobacterial progenitors that evolved into mitochondria, providing enhanced energy production and enabling greater cellular complexity.^[22] This symbiosis, along with later acquisitions like photosynthetic bacteria forming chloroplasts in some lineages, underscores how prokaryotes served as foundational contributors to eukaryotic evolution.^[23]

Cellular Structure

Cell Envelope

The cell envelope of prokaryotes serves as the outermost barrier, encompassing the plasma membrane and associated structures that provide structural integrity, protection, and selective permeability. This multilayered assembly is essential for maintaining cellular homeostasis in diverse environments.^[24] The plasma membrane, a phospholipid bilayer embedded with proteins, forms the innermost component of the cell envelope in all prokaryotes. It regulates the transport of nutrients and waste, facilitates energy generation through processes like electron transport, and supports biosynthesis of cellular components. Unlike eukaryotic membranes, prokaryotic plasma membranes typically lack sterols, except in certain Mycoplasma species.^[24] External to the plasma membrane lies the cell wall, which imparts rigidity and shape while countering osmotic pressure. In Bacteria, the primary constituent is peptidoglycan, a polymer of N-acetylglucosamine and N-acetylmuramic acid cross-linked by peptide bridges, unique to this domain except in wall-less genera like Mycoplasma. Bacterial cell walls exhibit two major variations: Gram-positive bacteria possess a thick peptidoglycan layer (20-80 nm) interspersed with teichoic acids, providing robust protection against lysis. In contrast, Gram-negative bacteria feature a thin peptidoglycan layer (5-10 nm) overlaid by an outer membrane containing lipopolysaccharides (LPS), which contribute to endotoxic properties and barrier functions against antibiotics and host defenses.^[24]^[24] Archaea lack peptidoglycan and instead employ diverse wall compositions adapted to extreme conditions. Many archaea feature pseudomurein, a polymer similar to peptidoglycan but composed of N-acetyltalosaminuronic acid and glutamic acid, lacking D-amino acids and thus insensitive to lysozyme. Others rely on S-layers, paracrystalline arrays of glycoproteins or proteins that form a rigid lattice directly atop the plasma membrane, serving as the sole wall in many species and functioning in cell shape maintenance and molecular sieving.^[25]^[25] Additional external structures include the glycocalyx, a polysaccharide-rich layer that may manifest as capsules or slime layers. Capsules are densely organized and firmly attached, often up to 10 µm thick, enhancing adhesion and shielding against phagocytosis, desiccation, and bacteriophages, as seen in Streptococcus pneumoniae. Slime layers are looser and more diffuse, primarily aiding in surface attachment and biofilm formation, such as in Pseudomonas aeruginosa. Collectively, these envelope components protect against osmotic stress, environmental toxins, and mechanical damage while enabling selective nutrient uptake through porins and transporters.^[24]^[26]^[24]

Cytoplasm and Internal Features

The cytoplasm of prokaryotes consists of a gel-like matrix enclosed by the cell membrane, lacking membrane-bound organelles such as those found in eukaryotes, and serving as the site for most cellular processes.^[27] It is densely packed with ribosomes, the nucleoid, and various inclusions, enabling efficient metabolic and synthetic activities in the absence of compartmentalization.^[24] The nucleoid is an irregularly shaped region within the cytoplasm that houses the prokaryotic genome, typically a single, circular chromosome of double-stranded DNA, without a surrounding nuclear membrane.^[24] In Bacteria, this DNA is compacted by nucleoid-associated proteins (NAPs) such as HU and H-NS, which facilitate supercoiling and looping to fit within the cell's dimensions, often spanning about 1 mm when fully extended but condensed into a structure roughly 1-2 µm in size.^[27] Archaea exhibit similar nucleoid organization, though with distinct histone-like proteins that form nucleosome-like structures for compaction.^[28] Electron cryotomography reveals varied nucleoid architectures, such as twisted spirals in Bdellovibrio bacteriovorus or parallel filament bundles in Leptospira species, aiding in spatial segregation from ribosomes.^[28] Ribosomes in prokaryotes are 70S particles, composed of 50S and 30S subunits, each about 18-20 nm in diameter, and are distributed throughout the cytoplasm, often forming polysomes for simultaneous translation of mRNA.^[24] These ribosomes, primarily composed of ribosomal RNA and proteins, synthesize proteins directly in the cytoplasm without association to an endoplasmic reticulum, with actively growing cells containing thousands per cell to support rapid protein production.^[27] In some species, such as Spiroplasma melliferum, a portion of ribosomes associates with the membrane, while in ultra-small bacteria, they cluster peripherally around a densely packed nucleoid.^[28] Inclusions are non-membrane-bound structures that store nutrients or provide specialized functions, varying by environmental needs.^[27] Common types include polyphosphate granules (metachromatic granules) for phosphate storage, poly-β-hydroxybutyrate (PHB) granules as carbon reserves in nutrient-rich conditions, and glycogen or polysaccharide deposits for energy.^[24] Gas vacuoles, found in certain aquatic cyanobacteria and halobacteria, consist of stacked protein cylinders that enhance buoyancy by lowering cell density.^[27] Other inclusions, like magnetosomes in magnetotactic bacteria, contain iron crystals for orientation in magnetic fields, while carboxysomes house enzymes for carbon fixation.^[27] Cryotomography shows these as spherical or coated granules without membranes, such as polyphosphate bodies in various Bacteria.^[28] Prokaryotes possess analogs to the eukaryotic cytoskeleton, including FtsZ, a tubulin-like GTPase that polymerizes into filaments forming a contractile Z-ring at the division site to mediate cytokinesis.^[28] Other elements include MreB, an actin homolog forming dynamic patches for cell shape maintenance, and crescentin for curvature in some rod-shaped cells, all contributing to spatial organization without true membrane-bound organelles like the Golgi apparatus.^[28] These proteins tether to the membrane and interact with the nucleoid to ensure proper intracellular positioning.^[28] Plasmids are small, extrachromosomal, circular DNA molecules that replicate independently of the chromosome and can carry genes for traits like antibiotic resistance or conjugation.^[27] They are common in Bacteria, with sizes ranging from a few to hundreds of kilobases, and are segregated during division via cytoskeletal-like proteins such as ParM filaments.^[28] In Archaea, plasmid-like elements exist but are less studied.^[27] Endospores, formed by certain Gram-positive Bacteria like Bacillus and Clostridium, are dormant, multilayered structures within the cytoplasm that confer resistance to extreme conditions such as heat and desiccation.^[24] These dehydrated spores contain a copy of the genome, ribosomes, and essential enzymes, encased in a peptidoglycan cortex and protein coat rich in dipicolinic acid and calcium for stability.^[27] Formation involves asymmetric division, but the spore itself represents a survival inclusion rather than an active reproductive unit.^[24]

Reproduction and Genetics

Asexual Reproduction

Prokaryotes primarily reproduce asexually through binary fission, a process that produces genetically identical daughter cells. The process begins with the replication of the circular chromosome, which starts at a single origin and proceeds bidirectionally until two complete copies are formed.^[29] As replication occurs, the chromosomes are segregated to opposite ends of the elongating cell through mechanisms involving proteins like ParA and ParB.^[30] Septum formation follows, initiated by the polymerization of FtsZ protein into a contractile Z-ring at the midcell, which recruits additional divisome proteins such as FtsA and ZipA to guide peptidoglycan synthesis and membrane invagination.^[31] Cytokinesis completes the division, cleaving the cell into two viable progeny, each receiving one chromosome copy.^[29] Under optimal conditions, such as nutrient-rich media at ideal temperatures, the entire binary fission cycle can occur in as little as 20 minutes, as observed in Escherichia coli.^[32] Variations on binary fission exist among prokaryotes, adapting to specific morphologies or environments. In budding, as seen in Caulobacter crescentus, an asymmetric division produces a motile swarmer cell and a stalked cell, with the daughter budding from a polar stalk rather than symmetrically.^[33] Filamentous prokaryotes, such as certain cyanobacteria, reproduce via fragmentation, where the elongated filament breaks into smaller segments that each develop into new cells.^[34] Sporulation, a survival mechanism in response to stress, occurs in members of the Firmicutes phylum, like Bacillus subtilis, where a mother cell engulfs a forespore to form a resistant endospore capable of dormancy until favorable conditions return.^[35] Unlike eukaryotic reproduction, prokaryotic asexual processes involve no meiosis or gamete fusion, ensuring clonal propagation.^[30] In batch cultures, prokaryotic populations exhibit distinct growth phases tied to asexual reproduction dynamics. The lag phase involves metabolic adaptation without significant division, as cells synthesize enzymes and repair damage from transfer.^[36] This transitions to the log (exponential) phase, where binary fission proceeds at the maximum rate, doubling cell numbers logarithmically until resources limit growth.^[37] The stationary phase follows, with division balancing cell death due to nutrient depletion or waste accumulation, maintaining a stable population.^[36] Eventually, the death phase ensues, marked by accelerated decline in viable cells from accumulated toxins.^[36] Environmental factors strongly influence the rate of prokaryotic asexual reproduction. Temperature modulates metabolic activity, with optimal ranges (e.g., 37°C for many mesophiles) accelerating fission, while extremes slow or halt it; for instance, psychrophilic prokaryotes maintain activity near 0°C but at reduced rates.^[38] Nutrient availability directly affects division speed, as carbon and nitrogen limitations extend the lag phase and reduce exponential growth rates by constraining DNA replication and protein synthesis.^[37] These factors collectively determine population dynamics without involving sexual elements like gametes.^[38]

Genetic Exchange and Variation

Prokaryotes generate genetic variation through horizontal gene transfer (HGT) mechanisms, which allow the exchange of genetic material between cells, complementing vertical inheritance and enabling rapid adaptation to environmental pressures. These processes include transformation, transduction, and conjugation, each facilitating the incorporation of exogenous DNA into the genome, often via homologous recombination. Additionally, mutations and recombination events introduce and shuffle genetic elements, driving evolution such as antibiotic resistance, while defense systems like CRISPR-Cas modulate HGT to balance plasticity and stability.^[39] Transformation involves the active uptake of free DNA from the environment by competent prokaryotic cells, a process documented in approximately 80 species across diverse phyla. During competence, cells express specialized proteins such as ComEA for DNA binding and ComEC for translocation across the membrane, internalizing single-stranded DNA that is then protected by DprA and integrated into the chromosome via RecA-mediated homologous recombination. This mechanism is regulated by signals like quorum sensing in Streptococcus pneumoniae or stress responses in Bacillus subtilis, enhancing genetic diversity without requiring cell contact and aiding adaptation, such as acquiring virulence factors.^[39]^[40] Transduction is a phage-mediated form of HGT where bacteriophages package and transfer bacterial DNA between cells. In generalized transduction, lytic phages like P22 in Salmonella mistakenly encapsulate random fragments of host chromosomal or plasmid DNA using pseudo-packaging sites, delivering them to recipient cells where recombination can occur, potentially transferring any genomic region at frequencies varying by site distribution. Specialized transduction, conversely, arises from temperate phages like lambda in E. coli, where imprecise prophage excision creates hybrid viral-host DNA molecules that package specific genes adjacent to the integration site, limiting transfer to those loci but occurring at low rates due to rare excision errors. Both types promote genetic exchange, accelerating the spread of traits like antibiotic resistance.^[41]^[42] Conjugation enables direct cell-to-cell DNA transfer via a type IV secretion system, exemplified by the F-plasmid in Escherichia coli. Donor cells (F+) assemble a conjugative pilus from F-pilin (TraA) and accessory proteins, bridging to recipient (F-) cells and forming a mating pair. At the origin of transfer (oriT), the relaxosome—comprising TraI relaxase, TraM, TraY, and integration host factor—nicks the plasmid, exporting a single-stranded T-strand through the pilus via the coupling protein TraD, while rolling-circle replication maintains the donor copy. In the recipient, the T-strand circularizes and replicates, often converting it to a donor and exponentially disseminating plasmids carrying resistance genes.^[43]^[44] Mutations and recombination further amplify genetic variation in prokaryotes, particularly in evolving antibiotic resistance. Point mutations, occurring at rates of 10^{-10} to 10^{-9} per base pair per generation, alter targets like penicillin-binding proteins in Streptococcus pneumoniae or β-lactamases in E. coli, while hypermutable strains with defective repair systems (e.g., 1% of natural E. coli populations) accelerate diversification. Recombination integrates acquired elements, forming mosaic genes such as aac(6′)/aph(2″) for aminoglycoside resistance or transferring CTX-M β-lactamases via plasmids and integrons, enabling rapid adaptation under selective pressure. These processes often impose fitness costs, mitigated by compensatory mutations, and drive the emergence of multidrug-resistant lineages.^[45]^[46] The collective outcomes of these mechanisms confer genome plasticity, allowing prokaryotes to evolve swiftly, as seen in the dissemination of resistance genes across ecosystems. However, CRISPR-Cas systems counter unchecked HGT by providing adaptive immunity, acquiring short spacer sequences from invaders like phages into CRISPR arrays via Cas1 and Cas2, then using guide RNAs with Cascade and effector nucleases (e.g., Cas3) to cleave matching foreign DNA. This defense restricts deleterious transfers while permitting beneficial ones, maintaining a dynamic balance in genome evolution and influencing microbial diversity.^[47]^[48]

Growth Forms and Interactions

Unicellular and Colonial Growth

Prokaryotes predominantly adopt a unicellular lifestyle, existing as free-living planktonic cells that disperse through aquatic or fluid environments to access nutrients and avoid localized depletion. These cells often exhibit motility to enhance foraging and evasion. In Bacteria, motility is primarily through flagella, which propel them via rotary motion in a run-and-tumble pattern. In Archaea, motility typically involves archaella, rotary structures analogous to but distinct from bacterial flagella, enabling swimming in diverse environments including hypersaline or high-temperature settings.^[49] For example, in bacteria such as Pseudomonas aeruginosa, flagella enable swimming speeds of up to 59 μm/s in bulk liquid, with stator proteins like MotAB and MotCD adapting propulsion near surfaces to maintain near-surface motility at around 55 μm/s. Gliding motility represents an alternative unicellular propulsion mechanism in certain bacteria, such as Flavobacterium johnsoniae, where cells move across solids using type IV pili or other adhesion complexes without visible appendages, achieving speeds of 2–10 μm/s through cyclic extension and retraction. This motility supports individual exploration in heterogeneous environments, such as soils or sediments, prior to any aggregation. In Archaea, some species like Halobacterium salinarum exhibit swimming via archaella at speeds up to 15 μm/s.^[50] Colonial growth emerges when unicellular prokaryotes transition to simple multicellular aggregates, often through clumping facilitated by surface adhesins that mediate cell-cell adhesion. Adhesins, including trimeric autotransporter adhesins like VtaA, VtaE, and VtaD in Veillonella parvula (a bacterium), bind to complementary proteins on partner cells, promoting coaggregation and the formation of clustered pellets or rafts. For instance, in oral bacteria, V. parvula adhesins interact with sortase-assembled adhesins like VisA on Streptococcus gordonii, leading to mixed-species clumps that initiate plaque-like structures. In photosynthetic prokaryotes, cyanobacterial mats arise from similar adhesion, where tubular pili in Microcystis aeruginosa bridge cells into micro-colonies, enhancing buoyancy and preventing sedimentation in water columns. Archaeal examples include aggregates in methanogenic Archaea like Methanosarcina, which form clusters via cell wall proteins for improved gas exchange in anaerobic environments.^[51] These bacterial and archaeal pellets, observed in environments like activated sludge, marine sediments, or anaerobic digesters, form transient aggregates of dozens to hundreds of cells, distinct from more structured communities. Coordination in colonial forms relies on quorum sensing, a chemical signaling system that triggers density-dependent behaviors once aggregates reach critical cell numbers. Prokaryotes release autoinducers, such as acyl-homoserine lactones (AHLs) in Bacteria, which accumulate extracellularly and activate gene expression at high densities. Archaea utilize different signaling molecules, like hydroxycinnamic acid derivatives in some species. In Vibrio fischeri (a bacterium), the AinS/AinR system produces octanoyl homoserine lactone (C8-HSL), which, upon threshold accumulation, induces bioluminescence via a cascade involving LuxR and the lux operon, synchronizing light emission for symbiotic counter-illumination in host squid. This signaling ensures collective responses, such as synchronized motility or enzyme production, optimizing group function without complex differentiation. Colonial aggregation confers key advantages, including enhanced protection and resource sharing, which can drive evolutionary transitions toward multicellularity in select lineages. Aggregates shield interior cells from predators, phages, and environmental stresses; for example, dense clusters in marine bacterium Vibrio splendidus resist protist grazing during algal blooms by maintaining structural integrity up to 40 μm in radius. Resource sharing is evident in collective degradation of complex polymers, where clumped cells pool extracellular enzymes—such as xylanases on xylan—retaining breakdown products locally to boost growth rates by increasing effective nutrient access for up to 110 cells per cluster. In V. splendidus, phenotypic specialization within aggregates partitions carbon storage (via polyhydroxyalkanoates) to a motile core, enabling dispersal and reproduction cycles that outperform solitary cells under nutrient limitation. Experimental evolution in Escherichia coli demonstrates how plastic clustering under salinity stress assimilates genetically via mutations in peptidoglycan genes like mraY, yielding obligate multicellular lines with 2–3 cm clusters after 50 generations, marking a prokaryotic shift to heritable group formation. Similar evolutionary potential exists in archaeal lineages, though less studied.^[52]

Biofilms and Multicellularity

Biofilms represent structured communities of prokaryotes, primarily bacteria but also including archaea, embedded in a self-produced extracellular polymeric substances (EPS) matrix that provides mechanical stability and protection. The EPS matrix, composed mainly of polysaccharides, proteins, and extracellular DNA, forms a hydrated gel-like network that encases microbial cells, facilitating adhesion to surfaces and creating microenvironments with nutrient gradients. This architecture includes layered structures with water channels that enable the flow of nutrients and waste, promoting the survival of cells in diverse conditions. Archaeal biofilms, such as those formed by Sulfolobus in acidic hot springs, exhibit similar EPS structures adapted to extreme conditions.^[53]^[54]^[55]^[56] The formation of biofilms occurs in distinct stages: initial attachment, where free-floating planktonic cells reversibly or irreversibly adhere to a surface via appendages like pili; maturation, involving microcolony development, EPS production, and three-dimensional structuring; and dispersion, where cells detach to colonize new sites. These stages are exemplified in dental plaque, a biofilm formed by oral bacteria such as Streptococcus mutans on tooth surfaces, leading to caries if unmanaged, and in water distribution systems, where biofilms of species like Pseudomonas aeruginosa accumulate in pipes, contributing to clogs and contamination. Archaeal biofilms contribute to structures like stromatolites in extreme environments. Quorum sensing coordinates these processes by regulating gene expression in response to cell density.^[57]^[58]^[59]^[60] Within biofilms, prokaryotes exhibit multicellular-like cooperation, including cellular differentiation into specialized types such as persister cells, which enter a dormant state to survive stressors. This differentiation enhances community resilience, notably conferring up to 1,000-fold greater antibiotic resistance compared to planktonic cells, as the EPS matrix impedes drug penetration and persisters tolerate treatments that kill active cells. Such behaviors underscore biofilms' role in chronic infections.^[61]^[62]^[63] Evolutionarily, biofilm formation is an ancient trait, likely predating the last universal common ancestor and intrinsic to early microbial life on Earth, as evidenced by fossilized stromatolites dating back over 3.5 billion years. This capability has driven prokaryotic diversification, enabling pathogenesis in hosts—such as in device-related infections—and bioremediation applications, where biofilm consortia degrade pollutants more effectively than free cells due to their stable, cooperative structure.^[64]^[65]

Metabolism and Physiology

Metabolic Pathways

Prokaryotes exhibit remarkable metabolic diversity, enabling them to thrive in varied environments through distinct strategies for energy generation and carbon acquisition. Autotrophic prokaryotes fix inorganic carbon, primarily carbon dioxide, to synthesize organic compounds, while heterotrophic ones derive carbon from pre-existing organics. This versatility stems from adaptations in core biochemical pathways, allowing exploitation of light, inorganic chemicals, or organic substrates under aerobic or anaerobic conditions.^[66] Photoautotrophic prokaryotes, such as cyanobacteria, harness light energy using chlorophyll a to drive photosynthesis, producing oxygen and fixing CO₂ via the Calvin-Benson-Bassham cycle. This process involves light-dependent reactions that generate ATP and NADPH, followed by the cycle's carboxylation of ribulose-1,5-bisphosphate by RuBisCO to incorporate CO₂ into sugars. Cyanobacteria, like Synechococcus species, represent a key example, contributing significantly to global oxygen production and primary productivity in aquatic ecosystems. In contrast, anoxygenic phototrophic prokaryotes, such as purple sulfur bacteria (e.g., Chromatium) and green sulfur bacteria (e.g., Chlorobium), use bacteriochlorophylls to capture light energy without producing oxygen. They typically employ H₂S or organic compounds as electron donors in cyclic or noncyclic photophosphorylation and fix CO₂ via the Calvin cycle or reductive tricarboxylic acid (rTCA) cycle.^[66] Chemoautotrophic prokaryotes obtain energy from oxidizing inorganic compounds, such as ammonia or nitrite, while fixing CO₂ through the same Calvin cycle or variants like the reductive tricarboxylic acid (rTCA) cycle. Nitrifying bacteria, including Nitrosomonas (ammonia oxidizers) and Nitrobacter (nitrite oxidizers), exemplify this, using the energy from NH₄⁺ to NO₂⁻ or NO₂⁻ to NO₃⁻ oxidation to support autotrophic growth.^[67]^[68]^[69]^[70] Heterotrophic prokaryotes catabolize organic compounds for carbon, with chemoheterotrophs obtaining energy from chemical oxidation and photoheterotrophs using light. Chemoheterotrophs, often acting as saprophytes decomposing dead matter or parasites deriving nutrients from hosts, rely on pathways like glycolysis, which breaks down glucose to pyruvate yielding a net 2 ATP, followed by either fermentation or respiration. Fermentation regenerates NAD⁺ anaerobically, producing end products like lactate in Lactobacillus or ethanol in Zymomonas, but yields minimal ATP. Respiration, prevalent in aerobes like Escherichia coli, couples pyruvate oxidation via the tricarboxylic acid (TCA) cycle—generating NADH and FADH₂—to an electron transport chain (ETC) that uses O₂ as the terminal acceptor, achieving up to 38 ATP per glucose molecule. TCA cycle variants exist, such as the reductive branch in some anaerobes or incomplete cycles in obligate fermenters, reflecting metabolic flexibility.^[66] Photoheterotrophs, such as purple nonsulfur bacteria (e.g., Rhodobacter), generate energy through anoxygenic photosynthesis but acquire carbon from organic compounds in the environment.^[71] Anaerobic respiration and specialized processes further diversify prokaryotic metabolism. Many prokaryotes employ alternative ETC terminal acceptors like nitrate (NO₃⁻) in denitrifying bacteria such as Pseudomonas, reducing it to N₂, or sulfate (SO₄²⁻) in sulfate-reducing bacteria like Desulfovibrio, producing H₂S. These processes support energy conservation via proton motive force, though with lower efficiency than aerobic respiration. Methanogenesis, unique to certain archaea in the phylum Euryarchaeota (e.g., Methanococcus), reduces CO₂ or acetate to methane (CH₄) using H₂ or formate as electron donors, via a series of coenzyme-bound intermediates in a specialized pathway distinct from bacterial respiration. This archaeal metabolism is crucial in anaerobic environments like sediments and ruminant guts. Electron transport chains in prokaryotes vary widely, incorporating diverse carriers like cytochromes or quinones to accommodate acceptors such as O₂, NO₃⁻, or SO₄²⁻, enabling adaptation to oxygen gradients.^[66]^[72]^[73] Prokaryotic metabolic diversity extends to extremophiles, which possess unique enzymes optimized for harsh conditions. Thermophilic prokaryotes, such as Thermus aquaticus in hot springs, feature heat-stable enzymes including variants of glycolytic and TCA cycle components that maintain activity above 70°C. For instance, thermophilic DNA polymerases like Taq polymerase exemplify this robustness, though metabolic enzymes like thermostable RuBisCO in hyperthermophilic archaea ensure CO₂ fixation under extreme heat. These adaptations, often involving increased ionic bonds or hydrophobic cores in proteins, allow prokaryotes to occupy niches from deep-sea vents to acidic mines, underscoring their biochemical innovation.^[74]^[75]^[76]

Nutrient Uptake and Response to Environment

Prokaryotes employ diverse transport systems to acquire essential nutrients across their cell envelopes, particularly in nutrient-scarce environments. In Gram-negative bacteria, porins embedded in the outer membrane facilitate the passive diffusion of small hydrophilic molecules, such as sugars, amino acids, and ions, into the periplasmic space. These β-barrel proteins form water-filled channels that allow nonspecific or substrate-specific uptake, with pore sizes typically ranging from 6 to 10 Å in diameter, enabling efficient entry without energy expenditure. For instance, the OprD family of porins in Pseudomonas aeruginosa mediates the facilitated diffusion of basic amino acids like arginine and organic acids like pyroglutamate, becoming rate-limiting for growth under nutrient deficiency. Once in the periplasm, nutrients cross the inner cytoplasmic membrane via facilitated diffusion carriers or active transport systems. ABC (ATP-binding cassette) transporters, prevalent in both Gram-positive and Gram-negative prokaryotes, drive active uptake of a wide array of substrates—including amino acids, vitamins, and iron-siderophore complexes—against concentration gradients using ATP hydrolysis. In Escherichia coli, the maltose importer (MalFGK₂ with periplasmic binding protein MalE) exemplifies this, achieving up to a 10^6-fold concentration gradient for maltodextrins at submicromolar external levels. Another key system is the phosphoenolpyruvate:carbohydrate phosphotransferase system (PTS), which facilitates the active uptake and concomitant phosphorylation of sugars like glucose using phosphoenolpyruvate as the phosphate donor through a series of proteins (EI, HPr, EII). This group translocation mechanism is common in bacteria such as E. coli for efficient carbohydrate metabolism.^[77]^[78]^[79] To respond effectively to fluctuating environmental conditions, prokaryotes utilize sophisticated sensing and regulatory mechanisms that modulate transport and gene expression. Two-component systems, consisting of a sensor histidine kinase and a response regulator, detect external signals and trigger rapid physiological adjustments. The EnvZ/OmpR system in E. coli senses changes in osmolarity, with EnvZ autophosphorylating in response to increased osmolytes and transferring the phosphate to OmpR, which then regulates the expression of outer membrane porins ompF (favored at low osmolarity for broader nutrient access) and ompC (upregulated at high osmolarity for smaller pore selectivity). Alternative sigma factors, subunits of RNA polymerase, further fine-tune transcription during stress, prioritizing survival over rapid growth. In E. coli, the RpoS (σ^S) sigma factor is induced during nutrient limitation or stationary phase, activating hundreds of genes for cross-protection against starvation, oxidative damage, and osmotic stress; its levels are stabilized by small RNAs like DsrA and anti-adaptors such as IraP in response to the alarmone ppGpp, a starvation signal.^[80]^[81] Prokaryotic responses to nutrient deprivation often involve behavioral and morphological adaptations to optimize resource acquisition or enhance survival. Chemotaxis enables motile prokaryotes to navigate toward higher nutrient concentrations via biased random walks. In E. coli, methyl-accepting chemotaxis proteins (MCPs) detect temporal changes in attractants like amino acids or sugars, modulating flagellar rotation to extend "runs" up gradients (lasting ~1 second) while suppressing "tumbles" for reorientation, allowing detection of gradients as shallow as 1% change over 20 μm. Under prolonged starvation, certain Gram-positive prokaryotes, such as Bacillus subtilis, initiate sporulation—a complex differentiation process forming dormant endospores resistant to heat, desiccation, and chemicals. Triggered by nutrient exhaustion after vegetative growth, sporulation involves asymmetric division and sequential activation of sigma factors (σ^F, σ^E, σ^G, σ^K) under the master regulator Spo0A, completing in 8-10 hours to produce viable spores that germinate upon nutrient replenishment.^[82]^[83] Specific adaptations highlight prokaryotic ingenuity in nutrient uptake under challenging conditions. Many prokaryotes produce siderophores—low-molecular-weight chelators—to scavenge scarce iron (Fe^III), forming soluble complexes that are actively transported via ABC systems or TonB-dependent transporters. In marine environments, siderophores from diverse prokaryotes constitute a significant fraction of the iron-binding ligand pool, facilitating uptake in iron-limited waters and influencing global biogeochemical cycles. Acidophilic prokaryotes, thriving at external pH below 3, maintain cytoplasmic pH homeostasis near 6.0-7.0 through a reversed membrane potential (inside-positive) and impermeable lipid membranes that minimize proton influx, coupled with high-isoelectric-point surface proteins that electrostatically repel H^+. In Acidithiobacillus ferrooxidans, this is supported by adapted respiratory chains and ATP synthases optimized for alkaline internal conditions, ensuring continued nutrient transport despite acidic surroundings.^[84]^[85]

Ecology and Distribution

Habitats and Adaptations

Prokaryotes inhabit a vast array of environments, from commonplace settings to extreme conditions that challenge the limits of life. In terrestrial soils, they form diverse communities essential for nutrient cycling, with densities reaching up to 10^9 cells per gram in fertile topsoil. Oceanic habitats host the majority of global prokaryotic biomass, comprising over 90% of the living biomass in marine ecosystems, where they dominate the water column and sediments, driving primary production and carbon flux. Symbiotic associations are prevalent, particularly in animal gut microbiomes, where prokaryotes such as Bacteroides and Firmicutes constitute up to 10^14 cells per human host, aiding digestion and immune function.^[86]^[87] Extreme environments further highlight prokaryotic versatility. Thermophiles thrive in geothermal sites like hot springs and hydrothermal vents, with hyperthermophiles such as Methanopyrus kandleri strain 116 achieving growth at temperatures up to 122°C, the highest recorded for any organism. Halophiles dominate hypersaline locales, including salt lakes and evaporation ponds, where species like Halobacterium salinarum require salt concentrations exceeding 150 g/L for structural integrity and growth. Acidophiles, such as Acidithiobacillus ferrooxidans, flourish in acidic mine drainages and volcanic soils at pH levels below 3, maintaining cellular homeostasis despite proton influx.^[88]^[89]^[90] Key adaptations enable survival in these niches. In thermophiles, heat-stable proteins feature enhanced hydrophobic cores, increased ionic bonds, and disulfide bridges that prevent denaturation at high temperatures, as seen in enzymes from Pyrococcus furiosus. Halophiles employ compatible solutes like ectoine and trehalose for osmoprotection, balancing internal water potential without disrupting cellular processes in high-salt conditions. Extreme radiation resistance in Deinococcus radiodurans stems from robust DNA repair systems, including multiple genome copies and antioxidant defenses that neutralize reactive oxygen species, allowing recovery from doses up to 5,000 Gy.^[91]^[92]^[93] Prokaryotic biogeography reflects both ubiquity and niche specialization. They are globally distributed, from surface waters to the deep biosphere, yet cluster in tailored microhabitats; for instance, endolithic prokaryotes colonize rock interiors in arid deserts, such as cyanobacterial communities in Antarctic gypsum and volcanic stones, exploiting translucent minerals for photosynthesis while shielded from desiccation. This distribution underscores their role in pioneering inhospitable terrains, with genetic adaptations fine-tuned to local physicochemical gradients.^[94]^[95]

Ecological Roles

Prokaryotes play pivotal roles in nutrient cycling, facilitating the transformation and availability of essential elements in ecosystems. In the nitrogen cycle, diazotrophic prokaryotes such as Rhizobia form symbiotic associations with legume roots, converting atmospheric dinitrogen into ammonia through nitrogen fixation within specialized nodules, thereby enriching soil with bioavailable nitrogen for plant growth.^[5] Prokaryotes also drive decomposition by breaking down organic matter from dead plants and animals, recycling carbon, nitrogen, and other nutrients back into the soil and water systems, preventing nutrient lockup and supporting ecosystem productivity.^[3] Additionally, in marine environments, prokaryotes contribute to carbon sequestration by fixing and burying organic carbon in sediments via processes like the microbial carbon pump, where heterotrophic bacteria transform labile dissolved organic matter into refractory forms that persist for centuries, mitigating atmospheric CO2 levels.^[96] Prokaryotes engage in diverse symbiotic interactions that influence ecosystem dynamics and host health. Mutualistic symbioses include Rhizobia's nitrogen-fixing partnership with legumes and mycorrhiza helper bacteria, such as certain Pseudomonas species, which enhance arbuscular mycorrhizal fungi colonization on plant roots, improving nutrient uptake and plant resilience.^[97] In contrast, pathogenic prokaryotes like Salmonella enterica exploit host interactions to cause infections, invading epithelial cells and triggering inflammatory responses that disrupt gut homeostasis and lead to diseases such as salmonellosis.^[98] On a global scale, prokaryotes underpin major biogeochemical processes with far-reaching climatic effects. Cyanobacteria, including Prochlorococcus and Synechococcus, account for approximately 25% of oceanic primary production, generating oxygen and organic carbon that form the base of marine food webs and drive the biological carbon pump.^[99] Methanogenic archaea, thriving in anaerobic habitats like wetlands and sediments, produce methane—a potent greenhouse gas contributing about 30% of atmospheric CH4—through the reduction of CO2 or acetate, influencing global warming feedback loops.^[100] Prokaryotes' ecological functions extend to human applications, particularly in biotechnology and health. In bioremediation, prokaryotes such as Pseudomonas and Dehalococcoides species degrade pollutants like hydrocarbons and chlorinated solvents in contaminated sites, restoring environmental quality through natural metabolic pathways.^[101] The human microbiome, dominated by prokaryotes like Bacteroides and Lactobacillus, modulates immune responses, nutrient absorption, and pathogen resistance; dysbiosis in this community is linked to conditions such as inflammatory bowel disease and obesity, highlighting its role in maintaining host health.^[102]

Evolutionary History

Origins and Early Life

Prokaryotes are considered the earliest forms of cellular life on Earth, with the first evidence appearing approximately 3.5 to 3.8 billion years ago during the Archean eon.^[103] The last universal common ancestor (LUCA), from which all modern life descends, is reconstructed as a prokaryote-like organism that existed around 4.2 billion years ago, possessing basic metabolic capabilities and existing in an anaerobic environment before the divergence of Bacteria and Archaea.^[104] This timeline aligns with the rapid emergence of life shortly after Earth's oceans formed, suggesting prokaryotes played a foundational role in establishing biological processes on the young planet. Key evidence for these early prokaryotes comes from the geologic record, including stromatolites—layered structures formed by microbial mats—that date back to at least 3.45 billion years ago in the Strelley Pool Formation of Western Australia, indicating photosynthetic or chemosynthetic activity by ancient microbes.^[105] Microfossils, such as filamentous cellular structures preserved in cherts, provide direct morphological evidence; for instance, 3.465-billion-year-old Apex Chert deposits in Australia contain diverse prokaryotic-like filaments interpreted as early bacteria.^[106] Additionally, carbon isotopic signatures showing depletion in ¹³C (δ¹³C values ranging from -31‰ to -39‰ for the microfossils, with bulk organic matter around -27‰) in organic matter from these sites reflect biological fractionation during carbon fixation, a hallmark of prokaryotic metabolism, as seen in analyses of Apex Chert microfossils.^[107] The environmental conditions for prokaryote origins were predominantly anaerobic, with life likely emerging in warm, anoxic settings such as terrestrial geothermal fields featuring shallow pools of condensed vapor or deep-sea hydrothermal vents, where mineral-rich waters provided energy gradients for primitive metabolisms.^[108] The RNA world hypothesis posits that early life relied on RNA molecules for both genetic storage and catalysis before the evolution of DNA-based genomes in prokaryotes, marking a transition to more stable hereditary systems around the time of LUCA.^[109] A major milestone was the development of photosynthesis approximately 3.0 billion years ago, beginning with anoxygenic variants using electron donors like hydrogen sulfide and later evolving to oxygenic photosynthesis in cyanobacteria, which produced oxygen as a byproduct and profoundly altered Earth's atmosphere.^[110]

Prokaryotic Diversification

Prokaryotic diversification began with the divergence of the two primary domains, Bacteria and Archaea, estimated to have occurred around 3.5 billion years ago (Ga), shortly after the emergence of the last universal common ancestor (LUCA).^[111] This split marked a pivotal radiation, driven by adaptations to distinct geochemical environments in the Archean oceans, where early prokaryotes colonized diverse niches ranging from hydrothermal vents to shallow sediments. Horizontal gene transfer (HGT) played a central role in this early innovation, facilitating the rapid exchange of genetic material across lineages and enabling the acquisition of novel metabolic capabilities that accelerated diversification.^[112] For instance, HGT allowed prokaryotes to integrate genes for environmental sensing and stress response, promoting resilience in fluctuating primordial conditions and contributing to the emergence of specialized clades within each domain.^[113] A landmark event in prokaryotic evolution was the evolution of oxygenic photosynthesis by cyanobacteria around 2.7–3.0 Ga, which culminated in the Great Oxidation Event (GOE) approximately 2.4 Ga. This process, utilizing water as an electron donor to produce oxygen as a byproduct, fundamentally altered Earth's atmosphere from anoxic to oxygenated, exerting selective pressure on anaerobic prokaryotes and spurring metabolic radiations.^[114] The GOE triggered widespread adaptations, including the rise of aerobic respiration in various bacterial lineages, which harnessed oxygen as a terminal electron acceptor to yield higher energy efficiency compared to anaerobic pathways.^[115] This metabolic expansion, evolving independently multiple times, allowed prokaryotes to thrive in oxygenated niches and laid precursors for endosymbiotic events by fostering oxygen-tolerant lineages capable of intracellular associations.^[116] Parallel to these metabolic shifts, prokaryotes diversified through the evolution of extremophilic adaptations, enabling colonization of harsh environments like hypersaline lakes, acidic hot springs, and deep-sea vents. Extremophiles, such as thermophilic archaea and acidophilic bacteria, arose through genomic innovations including reinforced cell membranes and DNA repair mechanisms, often disseminated via HGT, which enhanced survival under polyextreme conditions.^[117] These adaptations not only expanded ecological breadth but also underscored prokaryotic resilience, with examples like halophilic archaea maintaining functional metabolisms at salt concentrations lethal to most life forms.^[118] In modern contexts, prokaryotic diversification continues unabated, exemplified by the rapid evolution of antibiotic resistance through HGT-mediated acquisition of resistance genes, such as beta-lactamases in pathogenic bacteria. This ongoing process highlights the dynamic nature of prokaryotic genomes, where selective pressures from human activities drive further radiations, mirroring ancient environmental challenges that shaped their early history.^[45]

Classification and Diversity

Taxonomic Framework

Prokaryotes are classified within a hierarchical taxonomic system that organizes them into two primary domains: Bacteria and Archaea. This framework, established by the three-domain system proposed by Carl Woese and colleagues based on ribosomal RNA sequencing, separates prokaryotes from eukaryotes while distinguishing between the two prokaryotic domains on molecular grounds. In 2024, the ICNP formally recognized kingdom-level ranks within these domains to accommodate increasing phylogenetic resolution.^[119] The domain Bacteria encompasses a vast array of phyla, with major groups including Proteobacteria, which are metabolically diverse and include pathogens like Escherichia coli and nitrogen-fixing symbionts; Firmicutes, comprising Gram-positive bacteria such as Bacillus and Clostridium species known for spore formation; and Actinobacteria, which include soil-dwelling actinomycetes like Streptomyces that produce antibiotics. These phyla represent significant portions of bacterial diversity, with Proteobacteria alone accounting for over 40% of described bacterial sequences in some environmental surveys.^[120]^[121] In contrast, the domain Archaea includes kingdoms such as Methanobacteriati (formerly part of Euryarchaeota, which harbor methanogens and halophiles like Methanococcus and Halobacterium adapted to extreme conditions) and Thermoproteota (reclassifying former Crenarchaeota, featuring hyperthermophiles such as Sulfolobus thriving in high-temperature environments). Archaea exhibit unique biochemical traits, like ether-linked lipids, that justify their separation from Bacteria. Prokaryotic nomenclature follows binomial conventions under the International Code of Nomenclature of Prokaryotes (ICNP), assigning each species a genus name (capitalized) and specific epithet (lowercase), italicized, such as Escherichia coli. This system ensures stability and universality, with validly published names tracked by the List of Prokaryotic Names with Standing in Nomenclature (LPSN). Bergey's Manual of Systematics of Archaea and Bacteria serves as a key reference, providing detailed descriptions and classifications based on current data.^[123]^[124] Classification criteria integrate phenotypic characteristics, such as cell morphology, Gram staining, and physiological traits like growth requirements, with genotypic methods, particularly 16S rRNA gene sequencing, which identifies evolutionary relationships through conserved and variable regions achieving over 90% genus-level resolution. Polyphasic taxonomy combines these approaches for robust delineation.^[125] Despite advances, challenges persist, including polyphyletic groupings where taxa like certain "green nonsulfur bacteria" do not form monophyletic clades under molecular scrutiny, necessitating revisions. Additionally, the majority of prokaryotic diversity remains uncultured, represented by over 100 candidate phyla identified via metagenomics, such as the Candidate Phyla Radiation (CPR), complicating formal taxonomy as these lineages lack isolates for phenotypic validation.

Phylogenetic Relationships

The phylogenetic relationships among prokaryotes have been elucidated primarily through molecular methods, beginning with the analysis of the 16S rRNA gene, which Carl Woese and colleagues used to establish the three-domain system of life, separating Bacteria and Archaea as distinct prokaryotic domains from Eukarya.^[126] This conserved ribosomal RNA sequence provides a universal phylogenetic marker due to its essential role in protein synthesis and slow evolutionary rate, allowing reconstruction of deep evolutionary divergences across prokaryotic lineages.^[127] More recent advances in whole-genome phylogenomics have supplemented 16S rRNA data by analyzing thousands of protein-coding genes or concatenated alignments from complete genomes, enabling higher-resolution trees that account for genome-wide signals.^[20] To root the prokaryotic tree, researchers infer the position of the last universal common ancestor (LUCA), often using ancient duplicated genes or outgroup comparisons, placing the root between the bacterial and archaeal domains.^[104] Key findings from these approaches reveal that Archaea share a closer evolutionary affinity with eukaryotes than with Bacteria, supported by shared informational genes in replication, transcription, and translation machineries.^[20] Within Bacteria, phylogenomic analyses delineate major supergroups, including Terrabacteria (encompassing phyla like Actinobacteria and Firmicutes, adapted to terrestrial environments) and Gracilicutes (including Proteobacteria and Cyanobacteria, often associated with aquatic or host-associated niches).^[128] These supergroups emerged from early divergences post-LUCA, with the bacterial root positioned between them based on genome content and ribosomal protein phylogenies.^[104] Horizontal gene transfer (HGT) profoundly influences prokaryotic phylogeny, resulting in mosaic genomes where genes from distant lineages are integrated, complicating vertical inheritance signals.^[129] This leads to discrepancies between gene trees (reflecting individual gene histories shaped by HGT) and species trees (inferred from core genomes), with up to 20-30% of prokaryotic genes potentially acquired laterally in some lineages.^[130] HGT is particularly rampant in environments like sediments or symbioses, fostering adaptive evolution but blurring phylogenetic boundaries.^[129] Despite these insights, unresolved challenges persist, notably the role of Asgard archaea in eukaryogenesis, where these lineages possess eukaryotic signature proteins and form a sister group to eukaryotes in phylogenomic trees, suggesting an archaeal host in eukaryotic origins.^[131] Additionally, metagenomic surveys uncover vast uncultured prokaryotic diversity, revealing novel phyla and candidate groups that expand the tree's breadth beyond cultured representatives, with estimates indicating over 90% of prokaryotic lineages remain unsampled.^[132]

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Database of Growth TEMPeratures of Usual and RAre Prokaryotes
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Bacteria and Archaea, Prokaryotic Diversity - OERTX
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Biological Nitrogen Fixation | Learn Science at Scitable - Nature
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Impacts of Gut Bacteria on Human Health and Diseases - PMC
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Bergey's Manual of Systematics of Archaea and Bacteria
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species concept for prokaryotes | FEMS Microbiology Reviews
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A geological timescale for bacterial evolution and oxygen adaptation
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Horizontal Gene Transfer in Prokaryotes: Quantification and ... - NCBI
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A metagenomics roadmap to the uncultured genome diversity in ...
Sep 19, 2018 · We performed metagenomic sequencing on soda lake sediments to give the first extensive overview of the taxonomic diversity found in these complex, extreme ...