Cryptomonas Nasuta

''Cryptomonas'' is the name-giving genus of the Cryptomonads established by German biologist Christian Gottfried Ehrenberg in 1831. The algae are common in freshwater habitats and brackish water worldwide and often form blooms in greater depths of lakes. The cells are usually brownish or greenish in color and are characteristic of having a slit-like furrow at the anterior. They are not known to produce any toxins. They are used to feed small zooplankton, which is the food source for small fish in fish farms. Many species of ''Cryptomonas'' can only be identified by DNA sequencing. ''Cryptomonas'' can be found in several marine ecosystems in Australia and South Korea.

Etymology

''Cryptomonas'' has the meaning of hidden small flagellates from “crypto” and “monas”.

Genome Structure

Species within ''Cryptomonas'' contain four genomes: the nuclear, the nucleomorph, the plastid, and mitochondrial genomes. The plastid genome contains 118 kilobase pairs and is a result of one endosymbiosis event of ancient red alga. The study of genome structures of the genus has contributed to the life-history dependent dimorphism of ''Cryptomonas'', which is discussed in details later in the section Dimorphism.

Functions

''Cryptomonas'' are also photolithotrophs that contribute to oxygenic carbon fixation making them greatly critical to the carbon levels of fresh water environments.

Reproduction

Replication of ''Cryptomonas'' occurs in early summer when fresh water species are also reproducing. ''Cryptomonas'' replicates via mitosis that only takes about ten minutes. Sexual reproduction is not observed in this genus as many other genera of Cryptophytes also do not reproduce sexually.

Cell Structure

Organisms are asymmetric with a transparent membrane on the outside. The membrane is not ciliated. ''Cryptomonas'' cells are fairly large; they average about 40 micrometers in size and often take the shape of an oval or ovoid. There are two flagella present, yet the two flagella are not equally sized. One is shorter and curled and the other one is longer and straight. The two flagella are fixed to the cell by four unique microtubular roots. In addition, the flagella are lined with small hairs that allow for better movement. There are also contractile vacuoles that control the flow of water in and out.

Two boat-shaped plastids are observed in the cells. In a secondary endosymbiosis event, the phagotrophic ancestor of the ''Cryptomonas'' presumably captured a red alga and reduced it to a complex plastid with four envelope membranes. The phycobilisomes of the former red algae were reduced until only phycoerythrin remained. Phycoerythrobilin, a type of red phycobilin pigment, is a chromophore discovered in cyanobacteria, chloroplasts of red algae and some Cryptomonads. Phycoerythrobilin is present in the phycobiliprotein phycoerythrin, the terminal acceptor of energy during the process of photosynthesis. The phycoerythrin was translocated into the thylakoid lumen with its chromophore composition altered; subsequently, phycobiliproteins with at least seven different absorption spectra evolved. ''Cryptomonas'' is distinguished by the purple phycoerythrin 566 as an accessory pigment, which gives the organisms a brownish color in appearance.

Behaviour

''Cryptomonas'' are large in size, grow rather slowly, and are limited in nutrients. It also migrates between depths of water in order to reach depths that are ideal for photosynthesis and bacteriograzing, as well avoiding organisms that are their predators. Typically, they are found at depths of up to 102 meters and in a temperature range of -1.4 to 1.5 degrees Celsius. ''Cryptomonas'' seem to grow and survive with little competition. ''Cryptomonas'' swim actively, and they rotate while moving and sometimes swim in helical motion.

Dimorphism

Life history-dependent dimorphism was first described in organisms in 1986. In ''Proteomonas'', another genus of Cryptophyceae, the two morphs revealed large differences in cell size which apparently led to its discovery and subsequent recognition. ''Cryptomonas'' has been discovered to be another genus that possesses the characteristic of dimorphism.

Traditionally, ''Cryptomonas'' was considered to be 3 separate genera: '' Chilomonas,'' ''Cryptomonas'' and '' Campylomonas''. Before further molecular analysis, ''Cryptomonas'' have been characterized by mainly morphological characters, such as cell size, cell shape, number and color of plastids. However, it was still difficult to define ''Cryptomonas'' due to insufficient understanding of morphological characters and less-than adequate visibility of living cells using light microscopy alone to observe the cell structures. Also, laboratories had lacked the condition to detect the different stages of particular organisms.

The furrow-gullet system was used as a standard for organization of genera for many years. Most other Cryptophyte genera have either furrow or gullet, but ''Cryptomonas'' is one of the genera that possess a combination of the two, creating a furrow-gullet complex. The furrow-gullet complex is used by the cells to digest food for smaller organisms. Also, ejectisomes are found to be surrounding the complex. Previously, different textures of furrow plates are used to classify genera. For example, a furrow plate (extending posteriorly along one side of the ventral furrow-gullet complex) has been described as “scalariform” in ''Campylomonas'' yet “fibrous” in ''Cryptomonas''. In addition, in ''Cryptomonas'', the inner periplast component consists of polygonal plates. In contrast, in ''Campylomonas'', the inner periplast component is a continuous sheet-like layer.

However, during later research, more evidence of both molecular phylogeny and morphology has been found to support the claim that the three genera should be considered one single dimorphic genus. Characters previously used to distinguish ''Cryptomonas'' from ''Campylomonas'' were found to occur together in dimorphic strains, such as the type of periplast (polygonal periplast plates versus a continuous periplast sheet), indicating that periplast types relate to different life-history stages of a single taxon. To evaluate the taxonomic significance of the type of periplast and other characters previously used to distinguish genera and species, molecular phylogenetic analyses have been used to study two nuclear ribosomal DNA regions (ITS2, partial LSU rDNA) and a nucleomorph ribosomal gene (SSU rDNA). The results of the phylogenetic study provide molecular evidence for a life history-dependent dimorphism in the genus ''Cryptomonas'': the genus ''Campylomonas'' represents the alternate morph of ''Cryptomonas''. ''Campylomonas'' and ''Chilomonas'' are reduced to synonyms of ''Cryptomonas''.

Further research

In addition to plastids containing phycoerythrobilin, campylomorphs, formerly genera ''Campylomonas'' and ''Chilomonas'', also contain a colorless plastid that lacks photosynthetic pigment: leucoplast.

Since the complete loss of photopigments clearly distinguishes the leukoplastidious cryptophytes from ''Cryptomonas'', the incorporation of “''Chilomonas''” with ''Cryptomonas'' has been highly debatable. Scientist have not yet found out an explanation of how leucoplasts disappear during later life stage and when they disappear.

Species

* '' Cryptomonas ampulla'' Playfair
* ''Cryptomonas anomala'' F.E.Fritsch, 1914
* '' Cryptomonas appendiculata'' Schiller, 1957
* '' Cryptomonas baltica'' (G.Karsten) Butcher, 1967
* '' Cryptomonas borealis'' Skuja, 1956
* ''Cryptomonas brevis'' J.Schiller
* ''Cryptomonas commutata'' (Pascher) Hoef-Emden, 2007
* '' Cryptomonas compressa'' Pascher, 1913
* '' Cryptomonas croatanica'' P.H.Campbell, 1973
* ''Cryptomonas curvata'' Ehrenberg, 1831
* '' Cryptomonas cylindracea'' Skuja, 1956
* '' Cryptomonas czosnowskii'' Kisselev
* '' Cryptomonas erosa'' Ehrenberg, 1832
* '' Cryptomonas gemma'' Playfair
* ''Cryptomonas gracilis'' Skuja
* '' Cryptomonas gyropyrenoidosa'' Hoef-Emden & Melkonian, 2003
* ''Cryptomonas marssonii'' Skuja, 1948
* '' Cryptomonas maxima'' Playfair
* '' Cryptomonas mikrokuamosa'' R.E.Norris, 1964
* '' Cryptomonas nasuta'' Pascher
* ''Cryptomonas oblonga'' Playfair
* ''Cryptomonas obovata'' Czosnowski, 1948
* '' Cryptomonas obovoidea'' Pascher, 1913
* '' Cryptomonas ovata'' Ehrenberg, 1832
* '' Cryptomonas paramaecium'' (Ehrenberg) Hoef-Emden & Melkonian, 2003
* ''Cryptomonas parapyrenoidifera'' Skuja
* ''Cryptomonas pelagica'' H.Lohmann
* '' Cryptomonas phaseolus'' Skuja, 1948
* ''Cryptomonas platyuris'' Skuja, 1948
* '' Cryptomonas profunda'' R.W.Butcher, 1967
* ''Cryptomonas prora'' W.Conrad & H.Kufferath
* '' Cryptomonas pyrenoidifera'' Geitler, 1922
* '' Cryptomonas rhynchophora'' (W.Conrad) Butcher
* ''Cryptomonas richei'' F.E.Fritsch, 1914
* ''Cryptomonas rostrata'' Skuja, 1948
* ''Cryptomonas splendida'' J.Czosnowski
* ''Cryptomonas tenuis'' Pascher
* ''Cryptomonas testacea'' P.H.Campbell, 1973
* '' Cryptomonas tetrapyrenoidosa'' Skuja, 1948

References

External links

Tree of Life: Cryptomonas

{{Taxonbar, from=Q1142294

Cryptomonad genera
Taxa named by Christian Gottfried Ehrenberg