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Chloroflexus aggregans | |
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Scientific classification | |
Domain: | Bacteria |
Phylum: | Chloroflexota |
Class: | Chloroflexia |
Order: | Chloroflexales |
Family: | Chloroflexaceae |
Genus: | Chloroflexus |
Species: | C. aggregans |
Binomial name | |
Chloroflexus aggregans Hanada et al. 1995 | |
Chloroflexus aggregans is a bacterium from the genus Chloroflexus which has been isolated from hot springs in Japan. [1]
The Chloroflexus aggregans name origins from aggregate forming strains indicative of a new species from the Chloroflexus genus. [2] The naming of the C. aggregans comes from the visible aggregates formed by the species. [2]
In 1995, Satoshi Hanada, Akira Hiraishi, Keizo Shimada, and Katsumi Matsuura discovered a new strain of the Chloroflexus genus, named as the Chloroflexus aggregans. [1] The researchers discovered two strains of this bacterial species: MD-66T and YI-9. [2] The "T" in MD-66T represents the type strain. [2] The former, MD-66T strain, was discovered from the Meotobuchi hot spring while the YI-9 strain was from the Yufuin hot spring. [2]
Phylogenetically, Chloroflexus bacteria are very distinct from green sulfur bacteria but are still taxonomic relatives. [1] Thus, there is some overlap between these groups. [1] For instance, the light harvesting systems responsible for photosynthesis in both groups rely on bacteriochlorophyll pigments. [3] Currently, the molecular phylogenetic data remains unknown for most Chloroflexus strains. [2] Moreover, Chloroflexus strains have not yet been isolated in axenic cultures—meaning, strains that are able to be grown in the absence of other types of species. [1] Currently, the closest known relative to C. aggregans is C. aurantiacus. [2]
The naming of the C. aggregans comes from the visible aggregates formed by the species. [2] At first, the researchers classified these microbes as the C. aurantiacus species because they had a similar morphological appearance. [2] In addition, they had a high degree of genetic similarity. [2] However, C. aggregans' production of mat-like aggregates when cultured in the researchers' lab suggested that it was a different species than C. aurantiacus, resulting in the discovery of a new species. [2]
Phenotypically, the species resembles the Chloroflexus aurantiacus bacteria. [1] Genotypically, the species' 16S rRNA sequences are 92.8% similar to C. aurantiacus. [1] Its genome is 4.7 Megabases (Mb). [4]
Chloroflexus aggregans have an extremely versatile mixotrophic metabolism. [5] This is an advantage for their environment, since the microbial mats they inhabit have constantly fluctuating conditions that follow a general daily cycle. [5] During the daytime, when light is abundant, it is their main energy source and C. aggregans exhibit photoautotrophy, photomixotrophy, and photoheterotrophy. [5] They perform photosynthesis through the use of their chlorosomes, which are large pigment-containing complexes that can harvest light. [6] During the afternoon, when there is less light and lower oxygen concentrations in the microbial mats, the bacteria switch to chemoheterophy and use oxygen as their final electron acceptor (O2 respiration). [5] At night, when light is not available and the microbial mats are anaerobic, the bacteria continue to exhibit a chemoheterotrophic metabolism, but it is instead based on fermentation. [5] Finally to complete their daily metabolic cycle, C. aggregans vertically migrate to the surface of their microbial mats, which are microaerobic, in the early morning. [5] Here, they switch to chemoautotrophy based on O2 respiration. [5] When exhibiting heterotrophy, C. aggregans can utilize a diverse range of organic substrates as their carbon source, but grow optimally when either yeast extract or Casamino Acids are used. [1]
Currently, C. aggregans are known to reside in microbial mats in freshwater hot springs, living closely associated with other microorganisms in multilayered sheets. [5] Specifically, they have been discovered and sampled from these hot springs in Japan. [5] They coexist with filamentous, unicellular cyanobacteria in these mats. [5] When exhibiting a heterotrophic metabolism, C. aggregans rely on organic substrates excreted from these cyanobacterial neighbors to obtain carbon for biosynthesis. [2] To occupy these hot springs, C. aggregans are thermophiles and isolated cultures have been shown to exhibit optimal growth between 50–60 °C (122–140 °F). [2] They are filamentous, meaning the cells grow into long rods that only divide terminally, forming unbranched, multicellular filaments. [7] Uniquely, these long filaments of C. aggregans then associate into dense, mat-like aggregates, setting the bacteria apart from other species of Chloroflexus. [2]
16S rRNA data has shown that bacterial species within the Chloroflexus genus are among the earliest bacteria that were able to perform photosynthesis. [4] However, much still remains unknown about Chloroflexus aggregans and its complete genome has yet to be fully sequenced. [4] Thus, continued study of this organism could be important to help elucidate the origins of photosynthesis in bacteria. [4] In addition, studying the broader evolutionary relationships of C. aggregans to other groups of early photosynthetic bacteria could help scientists build a phylogenetic tree of these related phyla, deducing their evolutionary order. [8] For instance, a study comparing the signature sequences in highly conserved proteins of photosynthetic bacteria found that organisms in the genus Chloroflexus evolved before cyanobacteria. [8] Resolving these phylogenies could further help scientists understand how photosynthesis developed. [8] Today, this process sustains almost all life on Earth by providing oxygen to the atmosphere and energy for organisms in higher trophic levels. [9] Therefore, it is highly valuable to study how this process first arose. [9]
Photosynthesis is a system of biological processes by which photosynthetic organisms, such as most plants, algae, and cyanobacteria, convert light energy, typically from sunlight, into the chemical energy necessary to fuel their activities. Photosynthetic organisms use intracellular organic compounds to store the chemical energy they produce in photosynthesis within organic compounds like sugars, glycogen, cellulose and starches. Photosynthesis is usually used to refer to oxygenic photosynthesis, a process that produces oxygen. To use this stored chemical energy, the organisms' cells metabolize the organic compounds through another process called cellular respiration. Photosynthesis plays a critical role in producing and maintaining the oxygen content of the Earth's atmosphere, and it supplies most of the biological energy necessary for complex life on Earth.
Cyanobacteria, also called Cyanobacteriota or Cyanophyta, are a phylum of autotrophic gram-negative bacteria that can obtain biological energy via oxygenic photosynthesis. The name "cyanobacteria" refers to their cyan color, which forms the basis of cyanobacteria's informal common name, blue-green algae, although as prokaryotes they are not scientifically classified as algae. They appear to have originated in a freshwater or terrestrial environment.
The green sulfur bacteria are a phylum, Chlorobiota, of obligately anaerobic photoautotrophic bacteria that metabolize sulfur.
The Chloroflexia are a class of bacteria in the phylum Chloroflexota. Chloroflexia are typically filamentous, and can move about through bacterial gliding. It is named after the order Chloroflexales.
Chloroflexus aurantiacus is a photosynthetic bacterium isolated from hot springs, belonging to the green non-sulfur bacteria. This organism is thermophilic and can grow at temperatures from 35 °C to 70 °C. Chloroflexus aurantiacus can survive in the dark if oxygen is available. When grown in the dark, Chloroflexus aurantiacus has a dark orange color. When grown in sunlight it is dark green. The individual bacteria tend to form filamentous colonies enclosed in sheaths, which are known as trichomes.
Bacteriochlorophylls (BChl) are photosynthetic pigments that occur in various phototrophic bacteria. They were discovered by C. B. van Niel in 1932. They are related to chlorophylls, which are the primary pigments in plants, algae, and cyanobacteria. Organisms that contain bacteriochlorophyll conduct photosynthesis to sustain their energy requirements, but the process is anoxygenic and does not produce oxygen as a byproduct. They use wavelengths of light not absorbed by plants or cyanobacteria. Replacement of Mg2+ with protons gives bacteriophaeophytin (BPh), the phaeophytin form.
Purple bacteria or purple photosynthetic bacteria are Gram-negative proteobacteria that are phototrophic, capable of producing their own food via photosynthesis. They are pigmented with bacteriochlorophyll a or b, together with various carotenoids, which give them colours ranging between purple, red, brown, and orange. They may be divided into two groups – purple sulfur bacteria and purple non-sulfur bacteria. Purple bacteria are anoxygenic phototrophs widely spread in nature, but especially in aquatic environments, where there are anoxic conditions that favor the synthesis of their pigments.
A chlorosome is a photosynthetic antenna complex found in green sulfur bacteria (GSB) and many green non-sulfur bacteria (GNsB), together known as green bacteria. They differ from other antenna complexes by their large size and lack of protein matrix supporting the photosynthetic pigments. Green sulfur bacteria are a group of organisms that generally live in extremely low-light environments, such as at depths of 100 metres in the Black Sea. The ability to capture light energy and rapidly deliver it to where it needs to go is essential to these bacteria, some of which see only a few photons of light per chlorophyll per day. To achieve this, the bacteria contain chlorosome structures, which contain up to 250,000 chlorophyll molecules. Chlorosomes are ellipsoidal bodies, in GSB their length varies from 100 to 200 nm, width of 50-100 nm and height of 15 – 30 nm, in GNsB the chlorosomes are somewhat smaller.
A microbial mat is a multi-layered sheet of microorganisms, mainly bacteria and archaea, or bacteria alone. Microbial mats grow at interfaces between different types of material, mostly on submerged or moist surfaces, but a few survive in deserts. A few are found as endosymbionts of animals.
The Chloroflexota are a phylum of bacteria containing isolates with a diversity of phenotypes, including members that are aerobic thermophiles, which use oxygen and grow well in high temperatures; anoxygenic phototrophs, which use light for photosynthesis ; and anaerobic halorespirers, which uses halogenated organics as electron acceptors.
Anoxygenic photosynthesis is a special form of photosynthesis used by some bacteria and archaea, which differs from the better known oxygenic photosynthesis in plants in the reductant used and the byproduct generated.
Rhodovulum sulfidophilum is a gram-negative purple nonsulfur bacteria. The cells are rod-shaped, and range in size from 0.6 to 0.9 μm wide and 0.9 to 2.0 μm long, and have a polar flagella. These cells reproduce asexually by binary fission. This bacterium can grow anaerobically when light is present, or aerobically (chemoheterotrophic) under dark conditions. It contains the photosynthetic pigments bacteriochlorophyll a and of carotenoids.
Chlorobaculum tepidum, previously known as Chlorobium tepidum, is an anaerobic, thermophilic green sulfur bacteria first isolated from New Zealand. Its cells are gram-negative and non-motile rods of variable length. They contain chlorosomes and bacteriochlorophyll a and c.
Roseiflexus castenholzii is a heterotrophic, thermophilic, filamentous anoxygenetic phototroph (FAP) bacterium. This species is in one of two genera of FAPs that lack chlorosomes. R. castenholzii was first isolated from red-colored bacterial mats located Nakabusa hot springs in Japan. Because this organism is a phototroph, it utilizes photosynthesis to fix carbon dioxide and build biomolecules. R. castenholzii has three photosynthetic complexes: light-harvesting only, reaction center only, and light-harvesting with reaction center.
Arsenate-reducing bacteria are bacteria which reduce arsenates. Arsenate-reducing bacteria are ubiquitous in arsenic-contaminated groundwater (aqueous environment). Arsenates are salts or esters of arsenic acid (H3AsO4), consisting of the ion AsO43−. They are moderate oxidizers that can be reduced to arsenites and to arsine. Arsenate can serve as a respiratory electron acceptor for oxidation of organic substrates and H2S or H2. Arsenates occur naturally in minerals such as adamite, alarsite, legrandite, and erythrite, and as hydrated or anhydrous arsenates. Arsenates are similar to phosphates since arsenic (As) and phosphorus (P) occur in group 15 (or VA) of the periodic table. Unlike phosphates, arsenates are not readily lost from minerals due to weathering. They are the predominant form of inorganic arsenic in aqueous aerobic environments. On the other hand, arsenite is more common in anaerobic environments, more mobile, and more toxic than arsenate. Arsenite is 25–60 times more toxic and more mobile than arsenate under most environmental conditions. Arsenate can lead to poisoning, since it can replace inorganic phosphate in the glyceraldehyde-3-phosphate --> 1,3-biphosphoglycerate step of glycolysis, producing 1-arseno-3-phosphoglycerate instead. Although glycolysis continues, 1 ATP molecule is lost. Thus, arsenate is toxic due to its ability to uncouple glycolysis. Arsenate can also inhibit pyruvate conversion into acetyl-CoA, thereby blocking the TCA cycle, resulting in additional loss of ATP.
Chlorobium chlorochromatii, originally known as Chlorobium aggregatum, is a symbiotic green sulfur bacteria that performs anoxygenic photosynthesis and functions as an obligate photoautotroph using reduced sulfur species as electron donors. Chlorobium chlorochromatii can be found in stratified freshwater lakes.
"Erythrobacter tepidarius" is a moderately thermophilic and non-motile bacteria from the genus of Erythrobacter which has been isolated from a hot spring in Usami in Japan.
Roseiflexus is a genus of bacteria in the family Roseiflexaceae with one known species.
Chloroflexus islandicus is a photosynthetic bacterium isolated from the Strokkur Geyser in Iceland. This organism is thermophilic showing optimal growth at 55 °C (131 °F) with a pH range of 7.5 – 7.7. C. islandicus grows best photoheterotrophically under anaerobic conditions with light but is capable of chemoheterotrophically growth under aerobic conditions in the dark. C. islandicus has a yellowish green color. The individual cells form unbranched multicellular filaments about 0.6 μm in diameter and 4-7 μm in length.
Prosthecochloris aestuarii is a green sulfur bacterium in the genus Prosthecochloris. This organism was originally isolated from brackish lagoons located in Sasyk-Sivash and Sivash. They are characterized by the presence of "prosthecae" on their cell surface; the inner part of these appendages house the photosynthetic machinery within chlorosomes, which are characteristic structures of green sulfur bacteria. Additionally, like other green sulfur bacteria, they are Gram-negative, non-motile, and non-spore forming. Of the four major groups of green sulfur bacteria, P. aestuarii serves as the type species for Group 4.