Roseiflexus castenholzii | |
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Scientific classification ![]() | |
Domain: | Bacteria |
Phylum: | Chloroflexota |
Class: | Chloroflexia |
Order: | Chloroflexales |
Family: | Roseiflexaceae |
Genus: | Roseiflexus |
Species: | R. castenholzii |
Binomial name | |
Roseiflexus castenholzii Hanada et al., 2002 | |
Roseiflexus castenholzii is a heterotrophic, thermophilic, filamentous anoxygenetic phototroph (FAP) bacterium. [1] This species is in one of two genera of FAPs that lack chlorosomes. [2] [3] R. castenholzii was first isolated from red-colored bacterial mats located Nakabusa hot springs in Japan. [1] 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. [4]
This bacterium has a cell diameter is of 0.8–1.0 micrometers but does not have a definite length because of its multicelluar filamentous structure. The bacterium is red to reddish-brown forms distinct red bacterial mats in the natural environment. [2] R. castenholzii lacks internal vesicles, internal membranes, and complex structures. This species has gliding motility. [1]
The five currently known genera of FAP organisms are Chlorofelxus, Choronema, Oscillochloris, Roseiflexus, and Heliothrix. Of these five, only two do not contain chlorosomes: Roseiflexus and Heliothrix. [3] Roseiflexus and Heliothrix are both red due to only having Bchl a as a photosyntheic pigment. In most other aspects, both phenotypically and genetically, the genera Roseiflexus and Heliothrix are different from each other. [3] Little is known about the taxonomy of the Roseiflexus genus due to it only containing one known species: Roseiflexus casternholzii.
When first discovered, Roseiflexuscastenholzii was isolated from the lowest layer of a three layered bacterial mat; the top two layers contained cyanobacteria and Chloroflexus spp. [3] These mats were found in multiple Japanese hot springs ranging in temperature from 45.5 °C to 68.5 °C and with a neutral to alkaline pH range. [1] [3]
This bacterium is able to grow photoheterotrophically under anaerobic light conditions and chemoheterotrophically under aerobic dark conditions. Optimal growth conditions for this organism are 50 °C and pH 7.5–8.0. The first isolated type strain was HLO8T (= DSM 13941T = JCM 11240T). [1] [2]
In order to conduct photosynthesis, Roseiflexuscastenholzii contains three different complexes: light-harvesting only (LH), reaction center only (RC) and light-harvesting with reaction center (LHRC). [4] In contrast to most other FAPs, R.castenholzii does not have chlorosomes, which contain great amounts of photosynthetic pigments. [4] Because chlorosomes can obstruct observations of photosynthetic complexes, Roseiflexuscastenholzii is considered a model organism to study the reaction centers FAPs have. [4]
The LHRC contains both light harvesting and reaction center peptides that allow for absorbing light and exciting electrons in one complex. [5] The light-harvesting complex contains antenna pigments that allow the bacterium to absorb light around 800 nanometers. [5] The majority of these pigments are bacteriochlorophyll (BChl). [4] The reaction center in Roseiflexuscastenholzii is closely related to the RC of Chloroflexusaurantiacus. R.castenholzii's RC complex contains three subunits: L, M, and a c-type cytochrome. It lacks the H subunit common in purple bacteria. [5] The RC also contains BChl and bacteriopheophytin (BPhe) pigments. [6] [4]
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.
Photosystems are functional and structural units of protein complexes involved in photosynthesis. Together they carry out the primary photochemistry of photosynthesis: the absorption of light and the transfer of energy and electrons. Photosystems are found in the thylakoid membranes of plants, algae, and cyanobacteria. These membranes are located inside the chloroplasts of plants and algae, and in the cytoplasmic membrane of photosynthetic bacteria. There are two kinds of photosystems: PSI and PSII.
Heliobacteria are a unique subset of prokaryotic bacteria that process light for energy. Distinguishable from other phototrophic bacteria, they utilize a unique photosynthetic pigment, bacteriochlorophyll g and are the only known Gram-positive phototroph. They are a key player in symbiotic nitrogen fixation alongside plants, and use a type I reaction center like green-sulfur bacteria.
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 photosynthetic reaction center is a complex of several proteins, pigments and other co-factors that together execute the primary energy conversion reactions of photosynthesis. Molecular excitations, either originating directly from sunlight or transferred as excitation energy via light-harvesting antenna systems, give rise to electron transfer reactions along the path of a series of protein-bound co-factors. These co-factors are light-absorbing molecules (also named chromophores or pigments) such as chlorophyll and pheophytin, as well as quinones. The energy of the photon is used to excite an electron of a pigment. The free energy created is then used, via a chain of nearby electron acceptors, for a transfer of hydrogen atoms (as protons and electrons) from H2O or hydrogen sulfide towards carbon dioxide, eventually producing glucose. These electron transfer steps ultimately result in the conversion of the energy of photons to chemical energy.
A light-harvesting complex consists of a number of chromophores which are complex subunit proteins that may be part of a larger super complex of a photosystem, the functional unit in photosynthesis. It is used by plants and photosynthetic bacteria to collect more of the incoming light than would be captured by the photosynthetic reaction center alone. The light which is captured by the chromophores is capable of exciting molecules from their ground state to a higher energy state, known as the excited state. This excited state does not last very long and is known to be short-lived.
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.
The Fenna–Matthews–Olson (FMO) complex is a water-soluble complex and was the first pigment-protein complex (PPC) to be structure analyzed by x-ray spectroscopy. It appears in green sulfur bacteria and mediates the excitation energy transfer from light-harvesting chlorosomes to the membrane-embedded bacterial reaction center (bRC). Its structure is trimeric (C3-symmetry). Each of the three monomers contains eight bacteriochlorophyll a molecules. They are bound to the protein scaffold via chelation of their central magnesium atom either to amino acids of the protein or water-bridged oxygen atoms.
Photosynthetic reaction centre proteins are main protein components of photosynthetic reaction centres (RCs) of bacteria and plants. They are transmembrane proteins embedded in the chloroplast thylakoid or bacterial cell membrane.
The antenna complex in purple photosynthetic bacteria are protein complexes responsible for the transfer of solar energy to the photosynthetic reaction centre. Purple bacteria, particularly Rhodopseudomonas acidophila of purple non-sulfur bacteria, have been one of the main groups of organisms used to study bacterial antenna complexes so much is known about this group's photosynthetic components. It is one of the many independent types of light-harvesting complex used by various photosynthetic organisms.
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.
Heliothrix oregonensis is a phototrophic filamentous, gliding bacterium containing bacteriochlorophyll a that is aerotolerant and photoheterotrophic.
Chloroflexales is an order of bacteria in the class Chloroflexia. The clade is also known as filamentous anoxygenic phototrophic bacteria (FAP), as the order contains phototrophs that do not produce oxygen. These bacteria are facultative aerobic. They generally use chemotrophy when oxygen is present and switch to light-derived energy when otherwise. Most species are heterotrophs, but a few are capable of photoautotrophy.
Chloroflexus aggregans is a thermophilic, filamentous, phototrophic bacterium that forms dense cell aggregates. Its type strain is strain MD-66.
In some forms of photosynthetic bacteria, a chromatophore is a pigmented(coloured), membrane-associated vesicle used to perform photosynthesis. They contain different coloured pigments.
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.