Morphology and ultrastructure of Paulinella
Morphological comparisons between Paulinella FK01 and M0880/a strains were done using scanning electron microscopy (SEM). The general morphological characters we observed for M0880/a (Fig. 1D, E) are similar to the original description  and a previous study . The test is ovoid (23 – 27 × 16 – 20 μm; n = 13) and covered with silica scale plates. The anterior end has a narrow aperture (3 – 5.6 μm) that is comprised of three oral scales (see asterisks in Fig. 1D) extending from the cell body as a "neck" (see N in Fig. 1D). Within this neck, two slightly curved oral scales abut each other between a membranous operculum with the third scale covering the edge of the two oral scales (Fig. 1E). Below the oral scales, five descending columns of scales cover the test. A total of 12 – 14 scales are found in each column with the first row containing four scales instead of five (see arrow head in Fig. 1D). The scales around the anterior and posterior cell regions are smaller than in the middle. Three or four rows of scales from the posterior end have dozens of pustules on the surface of each scale. The external surface of the rest of the body scales is smooth. The internal surface of the scales that are shown in Fig. 1D (see arrows in inverted scales) have 12 – 18 pores per scale which were reported as "sieve-plates" in a previous study .
SEM images of photosynthetic Paulinella strains FK01 (A – C) and M0880/a (D, E). FK01 is smaller in cell size than M0880/a (i.e., the scale bar is the same in A and D). Distinctive, multiple fine pores are present on the surface of scales of FK01...
Cells of strain FK01 are clearly distinguished from the original description of P. chromatophora (i.e., M0880/a). These Paulinella cells are of a relatively smaller size (15 – 17 × 10 – 11 μm; n = 17) than in M0880/a (see, Fig. 1A–C) and there are between 10 – 11 scales per column. There are more distinctive, multiple fine pores on the external surface of scales in FK01 than in M0880/a (see, Fig. 1B). The fine-pored external surface was reported in newly formed scales in the heterotrophic species P. ovalis . Another heterotrophic species, P. indentata has a single row of fine-pores along the scale but three or four rows on the end of the scales . There are five oral scales in the aperture (2.4 – 3.6 μm), which is comprised of two main scales between a membranous operculum and three thinner scales that cover the main oral scales (see asterisks in Fig. 1C). The oral scales of FK01 are not projected outward to the same extent as in M0880/a (Fig. 1A vs. 1D, indicated with N), and the first row of body scales consists of five not four scales (see arrow head in Fig. 1A, C). Pustules on the four rows of posterior scales (see double arrow in Figs. 1A–B) are more distinct than those in the M0880/a strain. The size of pustule-covered scales gradually increases from the centre to the outside in a counter-clockwise direction. Around 10 – 20 internal "sieve-plate" pores are also found in FK01 and are detectable in SEM images taken from outside the cell, particularly in the posterior region (see arrows in Fig. 1B).
Table 1 shows a comparison of key morphological characters from different Paulinella species. Traits such as cell size, number of scales per column, and number of oral scales have been used to define species. For example, P. intermedia is similar to P. ovalis in size and the number of scales per column but it differs from the latter species by possessing flat scales and a wider oral aperture . Due to the presence of two plastids in the cytosol, the FK01 and M0880/a strains are clearly distinguished from other Paulinella species. In turn, FK01 is distinct from M0880/a with regard to cell size, number of scales, number of oral scales, and by having distinct fine-pores in the body scales.
Molecular phylogenetic analysis
Given the obvious morphological differences described above, we used gene sequences to test the evolutionary relationship between the two strains. Multiple markers were used for this purpose and we first present maximum likelihood (ML) trees inferred from nuclear 18S rDNA and a concatenated data set of plastid 16S + 23S rDNA (Figs. 2A, B). Given that filose amoebae such as P. chromatophora and Euglypha are consistently recovered as members of the Rhizaria (e.g., [13,27]), we chose to include only 18S rDNA sequences from members of this putative supergroup . The 18S rDNA tree shows a monophyletic grouping of the two Paulinella strains, suggesting they share a common photosynthetic 'host' ancestor. This hypothesis is substantiated by the plastid rDNA tree (Fig. 2B), that shows a monophyletic grouping of M0880/a and FK01 as sister to Synechococcus- and Prochlorococcus-type cyanobacteria as previously described for M0880/a [22,34]. The 18S rDNA tree provides high bootstrap and Bayesian support (posterior probability > 0.95 for all thick nodes in the trees; 100% bootstrap support in both RAxML [RML] and PhyML [PML] analyses) for a clade that unites both P. chromatophora strains with a group of uncultured marine environmental samples (i.e., GenBank accession numbers; AB275059, EF526891, see ). Because there are no sequence data available from heterotrophic Paulinella species with a taxonomic identification, we could not provisionally identify the source of the environmental samples. However, given that all described photosynthetic P. chromatophora are derived from freshwater environments [14,19] and the present work], these environmental sequences likely represent a marine sister group within the Paulinellidae (e.g., P. ovalis, P. indentata [24,25]). The Paulinellidae is closely related (90% RML, PML) to other euglyphids such as Tracheoeuglypha, Cyphoderia, and Euglypha species.
(A) RAxML phylogenetic tree of nuclear 18S rDNA from Rhizaria with the root placed on the branch leading to the Foraminifera. (B) RAxML phylogenetic tree of a concatenated data set of plastid-encoded 16S + 23S rDNA with the root placed on the branch leading...
Trees inferred from actin and ftsZ protein sequences are shown in Figures 3 and 4, respectively. The actin tree provides both bootstrap and Bayesian support for the existence of a branch that unites M0880/a and FK01 (89% RML, 95% PML), which in turn is sister to other euglyphid taxa (57% RML, absence of Bayesian support) within the Rhizaria. The overall topology for Rhizaria actins (Fig. 3) is consistent with previous analyses . This monophyletic clade, although surrounded by many internal nodes that are only weakly supported, shows unequivocal sequence divergence between M0880/a and FK01. Pairwise analysis of synonymous (Ks) and non-synonymous (Ka) substitution rates between the Paulinella actin coding regions are 1.0023 and 0.0181, respectively (Ka/Ks = 0.0181). This ratio is comparable to actin sequence differences between two green algal Ostreococcus species (i.e., O. tauri vs. O. lucimarinus; Ks = 1.2489, Ka = 0.0085, Ka/Ks = 0.0068), two multicelluar liverworts (Pellia endiviifolia vs. P. borealis; Ks = 0.8396, Ka = 0.0037, Ka/Ks = 0.0044), and different genera of yeasts (Saccharomyces vs. Kluyveromyces, Ks = 0.4541, Ka = 0.0178, Ka/Ks = 0.0300; Saccharomyces cerevisiae vs. Pichia stipitis, Ks = 0.7798, Ka = 0.0221, Ka/Ks = 0.0283). These results suggest that M0880/a and FK01 are significantly diverged from each other and likely constitute distinct species. This hypothesis is consistent with the plastid-derived gene data for rDNA (Fig. 2B) and ftsZ (Fig. 4). Interestingly, the estimated Ks value between ftsZ sequences from M0880/a and FK01 exceed the expected confidence limits (i.e., >> 1.0) likely indicating these plastid-encoded genes are undergoing a high nucleotide substitution rate possibly as a result of the genome reduction process. Taken together, our results indicate that after the single acquisition of the photosynthetic organelle, the P. chromatophora ancestor gave rise to at least two distinct lineages.
RAxML phylogenetic tree of actin sequences from photosynthetic Paulinella spp. with the root placed on the branch leading to chromalveolate taxa (i.e., stramenopiles + alveolates). The numbers at the nodes show support values derived from a RAxML bootstrap...
RAxML phylogenetic tree of plastid-encoded ftsZ from photosynthetic Paulinella spp. with the root placed on the branch leading to Clostridia. The numbers at the nodes show support values derived from a RAxML bootstrap analysis followed by those from a...
To advance our understanding of photosynthetic Paulinella, we generated plastid-encoded 16S rDNA sequences from environmental samples from four different sites in Japan. We amplified the gene directly using a small number of cells that were manually isolated from materials collected at each site (see Methods and Materials). The expanded rDNA tree of photosynthetic Paulinella (Fig. 5) shows that all of the isolates cluster together with robust bootstrap and Bayesian support (99% RML, 98% PML) with a sister-group relationship to Synechococcus/Prochlorococcus, confirming the single origin of the plastid in these Paulinella. The phylogeny also indicates that the Paulinella isolates are split into two distinct clades. One clade includes the M0880/a strain that is closely related to isolates from Kaga and Kanazawa-1 and -2, whereas the second includes the newly isolated FK01strain and a field isolate from Lake Kawaguchi (HSY et al. unpublished data). This topology is surprising because it does not provide evidence for geographic separation (i.e., Germany vs. Japan), but rather shows the German strain M0880/a might share a most recent common ancestor with Japanese isolates (i.e., from Kanazawa and Kaga). It is possible, however, that photosynthetic Paulinella species are globally distributed and we simply lack data from other sites to demonstrate this result. In any case, our results suggest these fascinating organisms are unlikely to be a relict branch of filose amoebal evolution but may be broadly distributed with many more living taxa than previously thought. Assessing further the biodiversity of this group and providing a taxonomic description of species are key next steps in understanding the biology of Paulinella (HSY et al., work underway).
RAxML phylogenetic tree of plastid 16S rDNA from photosynthetic Paulinella spp. with the larger tree (available upon request from HSY) removed at the branch leading to cyanobacteria. The numbers at the nodes show support values derived from a RAxML bootstrap...
The following points highlight the three main types of locomotion exhibited by protozoans. The types of locomotion are: 1. Amoeboid Movement 2. Flagellar Movement 3. Ciliary Movement.
Protozoans: Type of Locomotion # 1. Amoeboid Movement:
In Amoeba, movement of the animal is made by the throwing of pseudopodium (Fig. 10.60), called amoeboid movement. This is the most primitive kind of movement which is caused by contractility and is also the characteristic of Sarcodina and many Sporozoa. In the direction of movement of Amoeba a new pseudopodium is formed and the pseudopodium at the opposite side gradually disappears.
Excepting a few Suctorians which are sessile in adult stage most protozoa possess definite locomotor organelles which are closely associated with the body surface.
These organelles are:
A pseudopodium may be defined as a temporary projection of a part of cytoplasm, mainly formed from the ectoplasm. These are characteristic organelles of Sarcodina, certain Sporozoa and many Mastigophora where the pellicle is ill defined. They act as locomotory and feeding organs.
Types of pseudopodia:
According to form, structure and activity four different kinds of pseudopodia are recognised (Fig. 10.59).
(c) Reticulopodium or Rhizopodium
(d) Axopodium or Actinopodium
(a) Lobopodium [Gk. lobes = lobe; podium = foot]:
It is a short, finger or tongue-like projection which is accompanied by a flow of endoplasm and ectoplasm. The pseudopodium is broad with rounded or blunt tips. The ectoplasmmic area is distinctly clear, called the hyaline cap. It is the characteristic of many amoebas such as Amoeba, Chaos, Entamoeba, Arcella, Difflugia.
(b) Filopodium [L.filo = a thread; podium = foot]:
The filopodium is a slender, thread-like or filamentous projection. It is formed by the ectoplasm alone and without a hyaline cap. The filaments are narrow and may be branched but do not anastomose, Filopodium is the characteristic in Filosea (e.g., Gromia, Euglypha etc.).
(c) Reticulopodium or Rhizopodium [L. reticulos = a net, podium = foot]:
Similar in structure to that of filopodium but the branches anastomose. The numerous branched and anastomosed pseudopodia form a dense network, help primarily in capturing the prey and the secondary function is locomotion. It is found in Elphidium.
(d) Axopodium or Actinopodium [Gk. axo = an axle; podium = foot; aktis = ray]:
It is a semi-permanent structure and is made up of an axial rod enveloped by cytoplasm. The axial rod is made up of a number of fibrils and arises either from the central part of the body or from the nucleus or nuclei in multinucleate forms or from an intermediate zone between ectoplasm and endoplasm. Axopodia are found in Actinophrys, Actinosphaerium, etc.
Mechanism of Amoeboid Movement:
Formation of pseudopodia:
In amoeboid progression, pseudopodia are formed in two different ways:
(a) Profluent and
(a) Profluent type:
In profluent type, the ectoderm bulges out as a blunt projection and endoplasm flows into this projection in an even manner. By profluent method a single pseudopodium (Limax) or many pseudopodia (Lobose) may be formed at a time.
(b) Eruptive type:
In eruptive type ectoplasm and endoplasm burst out in an eruptive manner by dissolving the cell surface. Eruptive type of pseudopodium is restricted to small forms of amoeba where the gelated ectoplasm layer is very thin.
The physiological manifestations in pseudopodia formation are explained with the help of the following theories:
(i) Surface tension theory
(ii) Sol-gel theory or Change of viscosity theory
(iii) Molecular folding and unfolding theory
(iv) Front contraction theory or Fountain zone theory
(v) Rear contraction and Hydraulic theory
(vi) Structure and Role of micro-fibrils
(vii) Actin and Mysin interaction theory
(viii) Osmotic theory of amoeboid flow.
(i) Surface tension theory:
This theory was proposed by Berthold in 1886 and supported by Butschli (1894) and Rhumbler (1898). In surface tension theory it is assumed that the pseudopodium is formed from any place on the surface of the body by the change of the surface tension. The protoplasm being a fluid, must have a tension at its surface to make the mass spherical.
The surface tension may be decreased at any point due to external or internal changes. At the point of low surface tension the fluid flows outwardly forming an outgrowth, called pseudopodium. In this way a new pseudopodium is formed and the animal moves in that direction. The whole phenomenon is comparable to ‘fountain streaming’.
The protoplasm is not a fluid, but a gel-like substance, so the surface tension theory cannot be applied to protoplasm.
(ii) Sol-gel theory or Change of viscosity theory:
This theory was proposed by Hyman (1917) and strongly supported by Pantin (1923-26), Mast (1925-31) and others.
According to this theory the body of the Amoeba is made up of 4-regions:
(a) The outer most thin and elastic cell membrane or plasma membrane,
(b) Plasmagel, an outer stiffer jelly-like region of the ectoplasm,
(c) The plasmasol, an inner more fluid region of the endoplasm and
(d) A hyalin fluid which is a clear ectoplasmic area between plasma membrane and plasmagel.
This theory assumes that the pseudopodium is formed by the change of sol to gel and gel to sol states in the peripheral cytoplasm. The tip of the pseudopodium controls the change.
During the formation of the pseudopodium the plasma membrane of Amoeba gets attached to the substratum by means of an adhesive secretion. A local reversion of plasmagel to plasmasol takes place at the anterior end by internal chemical reaction.
The gel at the anterior end becomes thinner and weak. The rest of the plasmagel exerts pressure on the weakened area. The contracting plasmagel of the posterior end is continuously changed into plasmasol and it flows forwards and breaks the weak gel.
Anteriorly the plasmagel tube is continuously regenerated by gelation of plasmasol and a new pseudopodium is formed. The animal then progresses forward with the help of the pseudopodium (Fig. 10.61).
Though the theory is most popular to the zoologists but the actual mechanism of reversion of gel to sol or vice versa could not be explained properly.
The amoeboid movement is related to the sol-gel transition of cytoplasm and various non-muscle contractile proteins, Ca++ ions and membrane receptors are involved in this.
Under normal or resting condition the ectoplasm remains in gel state in which the actin filaments are cross-linked with one another to form a complex network-like structure and sol-state condition of the endoplasm contains non cross-linked actin filaments.
(iii) Molecular folding and unfolding theory:
Goldacre and Lorch (1950) and Goldacre (1952) suggested that the protein molecules in Amoeba are present in folded and unfolded forms and explained the molecular basis of gelation (gel) and solation (sol) state of protoplasm of Amoeba. They suggested that the force which is generated by the contraction of the plasma tube, could not bring the locomotion of Amoeba alone.
The forces which are generated by the folding and unfolding of the protein molecules, could help in locomotion. The sol state of the protoplasm is due to the folding of protein molecules and the gel state is due to the unfolding of protein molecules.
The folding of protein molecules occurs at the rear end of the ectoplasm in Amoeba where the plasmagel converts into plasmasol which flows in front and by gelation it forms pseudopod.
The gelation takes place by the unfolding of the protein molecules within the tip of the advancing pseudopod where plasmasol is converted into more rigid plasmagel (Fig. 10.61).
Barrington (1967) has supported this theory stating that the required amount of energy during pseudopodia formation comes from adenosine triphosphate (ATP).
(iv) Front contraction theory or Fountain zone theory:
This theory was proposed by Allen in 1962. According to him the endoplasmic molecules start moving first at the anterior end before doing the same in the posterior end. So according to him the locomotion of Amoeba is not effected by the squeezing from behind- forwards. According to this theory, the endoplasm contains long, protein chains.
These chains contract at the anterior end and at this end the plasmasol changes into plasmagel by folding the protein chains. This plasmagel flows forward and touches the hyalin cap and again flows backward creating a fountain-like appearance.
This anterior region now develops a tension which is transmitted at the posterior end of the endoplasm. It is due to fountain-like movement of the gel, Amoeba is forced forward. The attachment of Amoeba to the substratum is necessary for locomotion.
(v) Rear contraction and Hydraulic theory (Proposed by Rinaldi and Jahn in 1963):
By observation and analysis of the motion pictures of granule movements in advancing pseudopodia they supported the concept of Mast (1923), but criticised the view of Allen (1962). According to them the contraction in gel at the posterior end gives rise to hydraulic pressure in sol.
This pressure is not equally distributed. It is highest at the posterior end, lowest at the anterior end and moderate in the middle. Gel at the posterior end always changes to sol due to contraction of the plasmagel and gel at the anterior end becomes thinner. Sol from the posterior end flows forward, breaks the gel of the anterior end and forms a new pseudopodium and brings about the forward movement of Amoeba.
(vi) Structure and Role of micro-fibrils in Amoeboid movement:
Pollard and Ito (1972) have reported that there are two types of microfilaments in the cytoplasm of Amoeba. Of which the larger ones are called myosin, which are 16 nm thick and concentrated at the posterior (uroid) region. Others are comparatively smaller and 5-8 nm thick, called actin which are distributed all over the cytoplasm.
Actin, a cellular protein forms the cytoskeleton of Amoeba or the cell. The actins exist in globular monomere condition called globular actin or G-actin and when exist as fibres, they are called fibre actin or F-actin. F-actins are polymer of G-actin.
(vii) Actin and Myosin interaction theory:
Huxley (1973) proposed that the amoeboid movement occurs due to the interactions of actin and myosin microfilaments in a mannar which is similar with the muscle of higher metazoan forms.
He also suggested that one kind of filaments glide on the other and these filaments are largely confined in the gel region of the ectoplasm. This gliding helps to pull the animal forward. The gliding as well as movement is enhanced by the addition of ATP and Ca++ or Mg++ ions.
Stochem (1982) reported that the plasmagel is constructed by the actin proteins and plasmasol by the myosin proteins. A hydrostatic pressure is created by the contraction of the actin filaments at the rear end which pushes the plasmasol of the myosin forward that forms the pseudopodium and brings about the locomotion of Amoeba.
(viii) Osmotic theory of amoeboid flow:
The sol-gel theory can be explained with the help of osmotic theory of amoeboid flow. The cytoplasm of Amoeba contains both actin and myosin protein molecules and their interaction helps in the formation of pseudopodia. During conversion from endoplasm to ectoplasm a mesh of actin filaments develops by the polymerization of actin molecules which form the rigid gelatinous condition of ectoplasm.
When the chemical signals bind to the membrane receptors, the ectoplasm transforms into endoplasm at the rear end by depolymerization. Then the myosin subunits bind to the actin molecules which transform the actin mesh into a contractile jacket that forces the fluid interior endoplasm forward.
The breakdown of actin network by depolymerization increases the osmotic pressure which draws water from the endoplasm to the periphery of the protoplasm of Amoeba that creates the extension of the cell forming a pseudopodium (Fig. 10.62). At present most of the zoologists such as Ruppert and Barnes (1994), Pechenik (2000) and others support this view.
Protozoans: Type of Locomotion # 2. Flagellar Movement:
Flagellar movement is performed by flagella and it is more advanced type than the amoeboid type.
“Flagella are extremely fine, thread-like or whip-like, highly vibratile, centriole based locomotor organelles”.
In general the flagella are long and their motion is whip-like undulations.
They occur in all mastigophorans and also in flagellated stages of some Sarcodina and Sporozoa.
Pitelka (1949, 1962) observed the following structures of the flagella of euglenoid organisms under light and electron microscopes.
Structure under Light Microscope:
The flagella are slender, filamentous extensions of the cytoplasm and are highly vibratile. The length of the flagellar state is about 150 µm. They consist of an inner elastic central axis called axoneme and an outer protective contractile cytoplasmic sheath.
The sheath is made up of fibrillar substances which is a semifluid matrix and the fibrils of the sheath frayed out laterally along the length of the flagella and these lateral hair-like projections of the flagellum are called mastigonemes or flimmer. The term mastigoneme was given by Deflandre (1934). The outer sheath is circular or more or less flattened in cross section.
According to the disposition of the mastigonemes the flagella are classified into following types (Fig. 10.63).
Flagella are without mastigonemes, e.g., Noctiluca.
Flagella with a single row of mastigonemes on one side of the flagellum (Fig. 10.63A), e.g., Euglena.
Flagella with two or more rows of mastigonemes on the sides (Fig. 10.63B), e.g., Peranema, Monas socialis.
Pitelka (1949) reported that no frayed mastigonemes in the flagellum of Peranema.
Flagellum does not bear any arrangement of mastigonemes but a terminal filament is seen (Fig. 10.63D), e.g., Polytoma, Chlamydomonas.
When the flagellum bears two rows of mastigonemes on the sides and the flagellum ends in a terminal filament without mastigonemes (Fig. 10.63C), e.g., Urcoclus.
Origin of the Flagellum:
A flagellum originates from a basal body or basal granule or sometimes called a kinetosome or blepharoplast or kinetonucleus which is compact and spherical in shape, and situated in the ectoplasm. The basal bodies are modified centrioles, contain DNA and have the power of self-replication.
Structure under Electron Microscope (Fig. 10.64):
(A) Ultrastructure of the axoneme:
The axoneme is composed of a bundle of microtubules (sometimes called fibrils) which extend from the base to the tip of the flagellum. The fibrils constitute a ring-like doublet peripheral microtubules which are situated around two central singlet microtubules (9/9+2).
In Trypanosome lewisi, the axoneme is composed of 8 fibrils. All the microtubules are protected by a protoplasmic sheath which is continuous with the plasma membrane or cell membrane.
The two central microtubules are protected by a central sheath and these microtubules remain separated each other and form the central shaft of the flagellum. The diameter of the axoneme is variable in different species. The peripheral doublet microtubules are separated from each other by 200 Å.
The central microtubules are circular in cross section and are about 200 Å in diameter. The peripheral doublets are ellipsoidal in cross section and each of the doublets is composed of two microtubules and are called A microtubule and B microtubule or A tubule and B tubule or sometimes, called sub-fibres.
A tubule (microtubule) is smaller, complete and remains at the inner side, but B tubule is larger, incomplete and remains at the outer side (Fig. 10.64B).
All the microtubules of the axoneme are composed of globular protein called tubulin. The tubulin is a dimer varying from 11 kilodaltons to 12 kilodaltons. Each dimer is formed of two monomers, namely α and β monomers or α is represented by A tubulin and β monomer is represented by B tubulin. The A tubule and B tubule are microtubules.
The inner A tubule of each peripheral doublet is composed of 13 proto-filaments and outer B tubule contains 10 to 11. These proto-filaments are the subunits of tubulin protein. A pair of arms called dynein arms which project from A tubule, arranged in a clockwise direction towards B tubule of the neighbouring doublet (Fig. 10.64B).
The dynein arms are called because the arms contain the dynein protein, similar to metazoan muscle myosin. The molecular weight of dynein is 5 x 105. The outer dynein arms are spaced at regular interval of 24 nm. The protein dynein contains a high molecular weight protein—ATPase, required Mg++ and Ca++ for its activity and is able to cleave ATP releasing chemical energy.
The central two microtubules are called namely C1 and C2 and may or may not be present. Nine delicate spokes extend from A tubule of each peripheral doublets and project towards the central sheath. These spokes are radially arranged and terminate into a head which may have a forked structure.
The adjacent two peripheral doublets are connected by an inter-doublet bridge, called nexin link, made up of an elastic protein nexin. The nexin links may act as stimulators which maintain the geometrical shape of the axoneme during the sliding motion.
(B) Ultrastructure of basal bodies:
The structure of basal bodies is comparable to the structure of the centriole. A cross section of the basal bodies (Fig. 10.64C) shows a ring of nine peripheral triplets. Each triplet is composed of 3 tubules, namely A, B and C. Tubule A appears circular in cross section while tubules B and C are crescent-shaped in outline. The tubules are microtubules.
A central cylinder-like structure without any singlet is called the hub. A and B tubules are elongated to form the doublet of the flagellum. From the hub nine radially arranged spokes originate which are connected to the peripheral triplets. The dynein arms are absent in triplets.
All the fibrils of the flagellum and cilia are anchored through the plate-like structure, called basal plate. The hair-like root-let fibres arise from the basal bodies which penetrate into the cytoplasm. The root-let fibres are contractile in nature and help to pull the flagellum or alter its orientation.
Modification of the structure:
The cytoplasmic sheath of Trypanosoma is cross striated. In Trichomonas and Trypanosoma a delicate membrane with vibratile nature which extends out from one side of the body, called undulating membrane and a flagellum always borders the outer margin of the membrane.
Number of flagella:
The number of flagella varies from species to species. The phytoflagellagtes usually have one or two flagella and zooflagellates bear one to many. Single flagellum is present in Trypanosoma, Leptomonas and Leishmania.
The two flagella are present in Cryptobia, and Ochromonas. Two to four flagella are present in Chilomastix and Retortamonas. Four to six flagella are seen in Trichomonas and Giardia, and numerous flagella are present in Trichonympha, a termite flagellate.
A mastigont system is a complex structure formed by groups of flagella and several microtubular and microfibrillar organelles is (e.g., Trichomonas, Trichonympha).
On the basis of attachment and direction of movement the flagella are of following types:
The flagella are generally originated from the anterior part of the body and the flagellum which is directed forward is called leading flagellum and its movement helps to pull the organism forward. Another flagellum orginating from the anterior end is directed backward is called trailing flagellum. This flagellum helps to steer the course of movement or trails behind, e.g., Bodo (Fig. 10.65).
When the flagellum is situated at the posterior end of the body and is used to push the body forwards by its vibration (e.g., Trypanosoma).
Process of Flagellar Locomotion:
The mechanism of flagellar locomotion (Fig. 10.67A-D) is not clearly known. As to the way in which a flagellum accomplishes locomotion there are four theories.
(a) Screw theory of Butschli:
It postulates a spiral turning of the flagellum like a screw resulting a propeller action which pulls the animal forward.
(b) Metzner’s theory:
Metzner has advocated that the flagellum beats in a circle tracing a cone and generates sufficient current to pull the animal forward.
(c) Theory of Ulehla and Krijsman:
According to this theory the ordinary movement of a flagellum is a sidewise lash consisting of an effective downward stroke followed by a relaxed recovery stroke by which the flagellum is brought forward again.
(d) Sliding tubule model:
This is the most widely accepted model. The sliding of the microtubules involves the movement of the flagellum. According to this theory, the peripheral microtubules form a linkage with each other and maintain a constant length.
The adjacent doublets slide past each other causing the entire flagellum to bend. The dynein arms of the doublets provide the sliding force and sliding involves the establishment of the cross-linkages (Fig. 10.66).
There is no doubt that flagellar waves pass from base to tip increasing in amplitude and velocity demonstrating that flagellum is an active unit that generates its own energy.
The flagellar movement has already described under the term “Locomotion in Euglena”.
Protozoans: Type of Locomotion # 3. Ciliary Movement:
Ciliary movement is exhibited by the beating of the cilia. It is the most advanced, complicated and co-ordinated mode of locomotion.
“Cilia are fine, short, hair-like, centriole-based protoplasmic processes, characteristic of many protozoan and metazoan cells”.
They are characteristic in Ciliata and larval Suctoria.
Structure of Cilia:
The cilia and flagella possess nearly the same structures except they differ in some points:
(i) Cilia are relatively shorter in length than the flagella.
(ii) Comparatively cilia are more numerous in number than the flagella. The cilia occur in patches or tracts but flagella generally occur singly or in pairs.
(iii) Absence of mastigonemes in cilia but present in flagella.
(iv) The microtubules of the axoneme extend from the base to the tip in flagellum but in cilium the microtubules are reduced in number towards the tip.
(v) Presence of kinetodesma in cilia but absent in flagella.
(vi) The movement of the flagella and cilia exhibit certain differences. Flagella exhibit undulating motion and beat independently but cilia in the longitudinal rows beat perpendicularly one after another (metachronous) and those in the transverse rows beat synchronously.
A. Under light microscope:
The cilia are fine, short, stiff, oar-like protoplasmic processes and emerge from the ectoplasm. The length of the cilia varies 10 µ to 15 µ. The cilia may be found all over the body (e.g., Paramoecium) or may be restricted to certain parts of the body (e.g., Vorticella).
The cilia are arranged in longitudinal, oblique or spiral rows, develop from either ridges or furrows. The ciliature can be divided into body or somatic ciliature (when the cilia occur over the body surface) and the oral ciliature which is confined to the mouth region.
The length of the cilia is uniform in Protociliates but in many ciliates the length is larger in certain parts of the body. A small row of close set cilia are found in some cases, called Pectinella.
Each cilium arises from a basal body or kinetosome which lies in the ectoplasm and consists of two parts:
(i) A basal body or kinetosome or kinetochore lies below to the cell membrane and
(ii) A shaft—short, threadlike structure lies above the pellicle.
The shaft varies 5-10 µm in length and 0.27 µm in breadth. In flagellum the shaft is about 150 µm in length.
B. Ultrastructure of cilium (Fig. 10.64):
The ultrastructure of a cilium is given by Satir (1968). The shaft of a cilium is composed of 9 fibrils or 9 paired microtubules, with central pair of single tubules, called the axoneme surrounded by a membrane which is continuous with the pellicle. A fine striated fibril called kinetodesma (PI. kinetodesmata) that connects each kinetosome or basal body and extends in the direction of an adjacent cilium of the same row.
The cilia, kinetosomes and kinetodesma together make up a kinety. The number of fibrils may exceed 500 in each kinetodesma. These fibrils are striated and form the framework of the cilium.
The axoneme is composed of a ring-like 9 doublet peripheral microtubules situated around two central singlet microtubules (9/9 + 2). The peripheral groups of microtubules or fibrils are radially arranged and are interspaced at 40° intervals. Each peripheral group consists of two microtubules which form a doublet. The two microtubules are called A microtubule or tubule and B microtubule or tubule.
The average diameter of microtubules vary from 180-250 Å. All the microtubules of the axoneme are composed of a globular protein, called tubulin.
A tubule (microtubule) of the peripheral group is smaller, complete and consists of 13 proto-filaments and B tubule is larger, incomplete and contains 10-11 proto-filaments or called tubulin subunits. The central two microtubules are unpaired separated each other and called C1 and C2 respectively.
The peripheral fibrils are ellipsoidal in cross section and central unpaired microtubules are circular in cross section. The tubulin protein is a dimer varying from 11,000 to 12,000 daltons. From the A microtubule of the doublets projects two processes called dynein arms.
The dynein are composed of a dynein protein. The dynein is an enzyme which degrades ATP to the ADP. The mol. wt. of dynein is 5 x 105. The microtubules are hollow and cylindrical in shape and peripheral group is composed of α and β tubulins.
The peripheral doublets are connected by nexin links which are composed of a protein called nexin. The molecular weight of the nexin is about 15 x 104. The function of the nexin link is unknown but they may serve as stimulators that maintain the geometric shape of the axoneme during the sliding motion.
Nine delicate spokes extend from A subfibril of each peripheral doublet towards the central sheath. These spokes are radially arranged and terminate into a forked structure, called radial spokes.
The ultrastructure of the basal body of the cilium is like that of an basal body of flagellum. In cross section the basal bodies consist of 9 peripheral triplet tubules. Each triplet consists of 3 tubules or microtubules. These tubules are named A tubule, B tubule and C tubule.
All free-swimming ciliates swim in a spiral path. During swimming an individual cilium bends throughout its length and strikes the water (Fig. 10.67 E-F). As a result the organism moves in a direction opposite to that of the effective beat and the dispelled water moves in the direction of the beat. The cilia in the longitudinal row move metachronously (wave-like action) and those in the transverse row act synchronously.
The ciliary movement has already been described under the term ‘Locomotion in Paramoecium’.
Views for Metachronous Rhythm:
There are two views regarding the controlling mechanisms of metachronous rhythm of cilia in Paramoecium.
1. Taylor’s neuroid fibre theory (1964):
He proposed that metachronous rhythmic movements of cilia are controlled by infraciliary system which co-ordinates the beating of cilia.
Naitoh and Eckert (1969) have stated that the role of infraciliary system has not been conclusively demonstrated.
2. Eckert’s electropotential theory (1972):
He has proposed that the potential differences are created by polarization and depolorization during an effective and a recovery stroke of each cilium which are responsible to maintain the metachronic rhythm.