Unicellular organism(Redirected from Unicellular life)
A unicellular organism, also known as a single-celled organism, is an organism that consists of only one cell, unlike a multicellular organism that consists of more than one cell. Historically, simple unicellular organisms have been referred to as monads, though this term is also used more specifically to describe organisms of the genus Monas and similar flagellate ameboids. The main groups of unicellular organisms are bacteria, archaea, protozoa, unicellular algae, and unicellular fungi. Unicellular organisms fall into two general categories: prokaryotic organisms and eukaryotic organisms. Unicellular organisms are thought to be the oldest form of life, with early protocells possibly emerging 3.8–4 billion years ago.
Prokaryotes, most Protista, and some fungi are unicellular. Although some of these organisms live in colonies, they don't exhibit specialization. These organisms live together, and each cell in the colony is the same. However, each individual cell must carry out all life processes to survive. In contrast, even the simplest multicellular organisms have cells that depend on each other to survive.
Most multicellular organisms have a unicellular life-cycle stage. Gametes, for example, are reproductive unicells for multicellular organisms. Additionally, multicellularity appears to have evolved independently many times in the history of life.
Candidatus Magnetoglobus multicellular, related to Deltaproteobacteria, is a multicellular prokaryote. It is neither unicellular, nor a colony.
Primitive cells, often referred to as protocells, are the precursors to today's unicellular organisms. Although the origin of life is largely still a mystery, in the currently prevailing theory, known as the RNA world hypothesis, early RNA molecules would have been the basis for catalyzing organic chemical reactions and self-replication. The RNA world hypothesis assumes that RNA molecules could form in abiotic conditions, which would require nucleic acids and ribose to be present. Theoretical and experimental findings show that nucleic acids and sugars could have been synthesized in early prebiotic conditions.
Compartmentalization was necessary for chemical reactions to be more likely as well as to differentiate reactions with the external environment. For example, an early RNA replicator ribozyme may have replicated other replicator ribozymes of different RNA sequences if not kept separate.
When amphiphiles like lipids are placed in water, the hydrophobic (water fearing) tails aggregate to form micelles and vesicles, with the hydrophilic (water loving) ends facing outwards. Primitive cells likely used self-assembling fatty-acid vesicles to separate chemical reactions and the environment. Because of their simplicity and ability to self-assemble in water, it's likely that these simple membranes predated other forms of early biological molecules.
Prokaryotes lack membrane-bound organelles, such as mitochondria or a nucleus. Instead, most prokaryotes have an irregular region that contains DNA, known as the nucleoid. Most prokaryotes have a single, circular chromosome, which is in contrast to eukaryotes, which typically have linear chromosomes. Nutritionally, prokaryotes have the ability to utilize a wide range of organic and inorganic material for use in metabolism, including sulfur, cellulose, ammonia, or nitrite. Prokaryotes as a whole are ubiquitous in the environment and exist in extreme environments as well.
Bacteria are one of the world’s oldest forms of life, and are found virtually everywhere in nature. Many common bacteria have plasmids, which are short, circular, self-replicating DNA molecules that are separate from the bacteria chromosome. Plasmids can carry genes responsible for novel abilities, of current critical importance being antibiotic resistance. Bacteria predominantly reproduce asexually through a process called binary fission. However, about 80 different species can undergo a sexual process referred to as natural genetic transformation. Transformation is a bacterial process for transferring DNA from one cell to another, and is apparently an adaptation for repairing DNA damage in the recipient cell. In addition, plasmids can be exchanged through the use of a pilus in a process known as conjugation.
The photosynthetic cyanobacteria are arguably the most successful bacteria, and changed the early atmosphere of the earth by oxygenating it. Stromatolites, structures made up of layers of calcium carbonate and trapped sediment left over from cyanobacteria and associated community bacteria, left behind extensive fossil records. The existence of stromatolites gives an excellent record as to the development of cyanobacteria, which are represented across the Archaean (4 billion to 2.5 billion years ago), Proterozoic (2.5 billion to 540 million years ago), and Phanerozoic (540 million years ago to present day) eons. Much of the fossilized stromatolites of the world can be found in Western Australia. There, some of the oldest stromatolites have been found, some dating back to about 3,430 million years ago.
Hydrothermal vents release heat and hydrogen sulfide, allowing extremophiles to survive using chemolithotrophic growth. Archaea are generally similar in appearance to bacteria, hence their original classification as bacteria, but have significant molecular differences most notably in their membrane structure and ribosomal RNA. By sequencing the ribosomal RNA, it was found that the Archeae most likely split from bacteria and were the precursors to modern eukaryotes, and are actually more phylogenetically related to eukaryotes. As their name suggests, Archeae comes from a Greek word archaios, meaning original, ancient, or primitive.
Some archaea inhabit the most biologically inhospitable environments on earth, and this is believed to in some ways mimic the early, harsh conditions that life was likely exposed to. Examples of these Archaean extremophiles are as follows:
- Thermophiles, optimum growth temperature of 50 °C-110 °C, including the genera Pyrobaculum, Pyrodictium, Pyrococcus and Melanopyrus.
- Psychrophiles, optimum growth temperature of less than 15 °C, including the genera Methanogenium and Halorubrum.
- Alkaliphiles, optimum growth pH of greater than 8, including the genus Natronomonas.
- Acidophiles, optimum growth pH of less than 3, including the genera Sulfolobus and Picrophilus.
- Piezophiles, (also known as barophiles), prefer high pressure up to 130 MPa, such as deep ocean environments, including the genera Methanococcus and Pyrococcus.
- Halophiles, grow optimally in high salt concentrations between 0.2 M and 5.2 M NaCl, including the genera Haloarcula, Haloferax, Halococcus.
Methanogens are a significant subset of archaea and include many extremophiles, but are also ubiquitous in wetland environments as well as the ruminant and hindgut of animals. This process utilizes hydrogen to reduce carbon dioxide into methane, releasing energy into the usable form of adenosine triphosphate. They are the only known organisms capable of producing methane. Under stressful environmental conditions that cause DNA damage, archaeal cells of some species aggregate and transfer DNA between cells. The function of this transfer appears to be to replace damaged DNA sequence information in the recipient cell by undamaged sequence information from the donor cell.
Eukaryotes are cells that contain membrane bound organelles, such as mitochondria, a nucleus, and chloroplasts. Prokaryotic cells transitioning into eukaryotic cells likely occurred between 2.0–1.4 billion years ago. This was an important step in evolution, which led to multicellularity of some eukaryotes into plants, animals and fungi. In contrast to prokaryotes, eukaryotes reproduce by using mitosis and meiosis. Sex appears to be a ubiquitous and ancient, and inherent attribute of eukaryotic life. Meiosis, a true sexual process, allows for efficient recombinational repair of DNA damage  and a greater range of genetic diversity by combining the DNA of the parents followed by recombination. Metabolic functions in eukaryotes are more specialized as well by sectioning specific processes into organelles.
Also important to eukaryotes is the endosymbiotic theory, which points out that mitochondria and chloroplasts likely have bacterial origins. Both organelles contain their own sets of DNA and have bacteria-like ribosomes. It's likely that modern mitochondria were once a species similar to Rickettsia, with the parasitic ability to enter a cell. However, if the bacteria were capable of respiration, it would have been beneficial for the larger cell to allow the parasite to live in return for energy and detoxification of oxygen. Chloroplasts probably became symbiants through a similar set of events, and are most likely descendants of cyanobacteria. While not all eukaryotes have mitochondria or chloroplasts, mitochondria are found in most eukaryotes, and chloroplasts are found in all plants and algae. Photosynthesis and respiration are essentially the reverse of one another, and the advent of respiration coupled with photosynthesis enabled much greater access to energy than fermentation alone.
Protozoa are largely defined by their method of locomotion, including flagella, cilia, and pseudopodia. While there has been considerable debate on the classification of protozoa caused by their sheer diversity, there are currently 7 phyla recognized under the kingdom protozoa: Euglenozoa, Amoebozoa, Choanozoa, Loukozoa, Percolozoa, Microsporidia and Sulcozoa. Protozoa, like plants and animals, can be considered heterotrophs or autotrophs. Autotrophs like Euglena are capable of producing their energy using photosynthesis, while heterotrophic protozoa consume food by either funneling it through a mouth-like gullet or engulfing it with pseudopods, a form of phagocytosis. While protozoa reproduce mainly asexually, some protozoa are capable of sexual reproduction. Protozoa with sexual capability include the pathogenic species Plasmodium falciparum, Toxoplasma gondii, Trypanosoma brucei, Giardia intestinalis and Leishmania species.
Ciliophora, or ciliates, are a group of protists that utilize cilia for locomotion. Examples include Paramecium, Stentors, and Vorticella. Ciliates are widely abundant in almost all environments where water can be found, and the cilia beat rhythmically in order to propel the organism. Many ciliates have trichocysts, which are spear-like organelles that can be discharged to catch prey, anchor themselves, or for defense. Ciliates are also capable of sexual reproduction, and utilize two nuclei unique to ciliates: a macronucleus for normal metabolic control and a separate micronucleus that undergoes meiosis. Examples of such ciliates are Paramecium and Tetrahymena that likely employ meiotic recombination for repairing DNA damage acquired under stressful conditions.
The Amebozoa utilize pseudopodia and cytoplasmic flow to move in their environment. Most Amebas are unicellular, although a few can become multicellular, such as Physarum polycephalum, a slime mold. Entamoeba histolytica is the cause of amebic dysentery. Entamoeba histolytica appears to be capable of meiosis.
- Euglenophyta, flagellated, mostly unicellular algae that occur often in fresh water. In contrast to most other algae, they lack cell walls and can be mixotrophic (both autotrophic and heterotrophic). An example is Euglena gracilis.
- Chlorophyta (green algae), mostly unicellular algae found in fresh water. The chlorophyta are of particular importance because they are believed to be most closely related to the evolution of land plants.
- Diatoms, unicellular algae that have siliceous cell walls. They are the most abundant form of algae in the ocean, although they can be found in fresh water as well. They account for about 40% of the world's primary marine production, and produce about 25% of the world's oxygen. Diatoms are very diverse, and comprise about 100,000 species.
- Dinoflagellates, unicellular flagellated algae, with some that are armored with cellulose. Dinoflagellates can be mixotrophic, and are the algae responsible for red tide. Some dinoflagellates, like Pyrocystis fusiformis, are capable of bioluminescence.
Unicellular fungi include the yeasts. Fungi are found in most habitats, although most are found on land. Yeasts reproduce through mitosis, and many use a process called budding, where most of the cytoplasm is held by the mother cell. Saccharomyces cerevisiae ferments carbohydrates into carbon dioxide and alcohol, and is used in the making of beer and bread. S. cerevisiae is also an important model organism, since it is a eukaryotic organism that's easy to grow. It has been used to research cancer and neurodegenerative diseases as well as to understand the cell cycle. Furthermore, research using S. cerevisiae has played a central role in understanding the mechanism of meiotic recombination and the adaptive function of meiosis. Candida spp. are responsible for candidiasis, causing infections of the mouth and/or throat (known as thrush) and vagina (commonly called yeast infection).
Macroscopic unicellular organismsEdit
Most unicellular organisms are of microscopic size and are thus classified as microorganisms. However, some unicellular protists and bacteria are macroscopic and visible to the naked eye. Examples include:
- Xenophyophores, protozoans of the phylum Foraminifera, are the largest examples known, with Syringammina fragilissima achieving a diameter of up to 20 cm (7.9 in)
- Nummulite, foraminiferans
- Valonia ventricosa, an alga of the class Chlorophyceae, can reach a diameter of 1 to 4 cm (0.4 to 2 in)
- Acetabularia, algae
- Caulerpa, algae
- Gromia sphaerica, amoeba
- Thiomargarita namibiensis is the largest bacterium, reaching a diameter of up to 0.75 mm
- Epulopiscium fishelsoni, a bacterium
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