Roseiflexus castenholzii | |
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Scientific classification ![]() | |
Domain: | Bacteria |
Kingdom: | Bacillati |
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]