4- Feeding in Protozoan (1).pptx subscribe my Youtube channel "Biology with kiran"

MaleehaKanwal1 374 views 34 slides Jul 16, 2024
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About This Presentation

Protozoa are a diverse group of single-celled eukaryotic organisms that can be found in various aquatic and terrestrial environments. Their feeding mechanisms are varied and adapted to their habitats and modes of life. Here is an overview of the feeding mechanisms in protozoa:

Modes of Nutrition in...


Slide Content

Feeding in Protozoan Protozoans may take food into the cell at a specific point, such as the cytostome (a well-developed feeding groove), at a particular region of the cell surface, or at any random point of entry. In the collared flagellates, or choanoflagellates, for example, the collar and flagellum operate in feeding. The collar, composed of fine pseudopodia, surrounds the flagellum. Fig : collar and flagellum in choanoflagellates Fig : cytostome In protozoans

Feeding in Protozoan The beating flagellum creates a water current, causing water to move through the  collar . Particles of food in the current are trapped on the collar and are ingested by pseudopodia at its base. The ingested food is then enclosed in a membrane-bound digestive or food vacuole. Fig : Particles of food in the current are trapped on the collar

Feeding in Protozoan Many ciliates are filter feeders, creating water currents with special ciliary structures associated with the cytostome . The synchronized beating of these ciliary structures pushes a stream of water against a membranelle composed of cilia. Fig : Synchronized beating of ciliary structures

Feeding in Protozoan The membranelle acts as a collecting sieve, where the food particles become trapped in the free spaces between the cilia. Using this mode of feeding, ciliates can shift considerable volumes of water in relation to their size. Tetrahymena, for example, can filter 3,000 to 30,000 times its own volume in one hour.

Feeding in Protozoan Other ciliates lack complex oral cilia and gather their food by other means.  Nassula  has a complex cytostome and cytopharynx supported by a basketlike cytopharyngeal structure composed of microtubules. This species ingests filamentous  algae  by grasping the filament, bending it like a hairpin, and drawing it into the cytopharynx, where it is broken up into fragments and enclosed in digestive vacuoles. Fig : Nassula

Feeding in Protozoan Predatory ciliates such as  Didinium nasutum ,  Lacrymaria olor , and  Dileptus anser   apprehend  their  prey  with special structures called  extrusomes . Among the various types of extrusomes are the  toxicysts , which are found in the oral region and release toxins that paralyze the prey. Fig : Extrusomes

Feeding in Protozoan The  suctorians  are  ciliate  predators that usually possess  tentacles  of two functional types: feeding tentacles and piercing tentacles. The latter trap and immobilize the prey, usually other ciliates that make chance contact with the outstretched tentacles of the  suctorian . Fig : Tentacles in Suctorians

Feeding in Protozoan The cell contents of the prey are transported up through the feeding tentacles into the suctorian, where digestive vacuoles are formed. The transporting mechanism is mediated by a complex array of microtubules within the tentacle. A single suctorian can often feed on several prey at the same time, and frequently the prey are larger than the predator.

Feeding in Protozoan Amoebae, all of which lack a cell mouth, or cytostome, also exhibit a  diverse  array of feeding mechanisms and diet. Some feed on filaments of cyanobacteria ( blue-green algae )—which are composed of long chains of individual cells—by taking in the entire filament at any point on the cell surface and rolling it up into a coil inside a digestive vacuole. Fig : Cell Mouth or Cytostome

Feeding in Protozoan Others, such as the  testate amoeba   Pontigulasia , pierce single cells in algal filaments and remove the contents. The radiolarians and foraminiferans trap a wide range of prey, including protozoans, algae, and small  crustaceans , in their complex pseudopodial networks and then transport the food items along the pseudopodia to the main body of the cell for ingestion. Fig : Foraminiferans Fig : Radiolarians

Feeding in Protozoan This process gives foraminiferans a distinctive appearance under the light microscope; relatively large grains of food particles are scattered across the reticulate pseudopodia, earning the organisms the name  granuloreticulosans .

Feeding in Protozoan Parasitic protozoans feed in a variety of ways. Many live in the nutrient-rich medium of the body fluids—e.g., the blood or cells of their host. There they take in energy-rich fluids by   pinocytosis , in which small amounts of the medium are pinched off into digestive vacuoles either at a specific site, such as the cytostome in ciliates or the flagellar pocket in trypanosomes, or along the surface of the cell in amoebae.

Feeding in Protozoan Other parasitic protozoans engulf portions of the host  tissue  through  phagocytosis  in much the same way that free-living amoebae feed.  Plasmodium , for example, engulfs portions of the  red blood cells  or liver cells in which they live. The hemoglobin in the cytoplasm of the red blood cell is only partially digested by the  parasite .

Feeding in Protozoan The  protein  portion of the hemoglobin molecule is degraded to its  constituent   amino acids , but the  iron -containing portion is converted into insoluble iron-containing hemozoin, which remains within the parasite’s endosomes until discarded at the next division. This process removes free hematin from the parasite cytoplasm, where it would otherwise prevent further metabolism within the parasite because it  inhibits  the actions of succinic dehydrogenase, an enzyme in the  tricarboxylic acid cycle .

Feeding in Protozoan Whatever the mode of heterotrophic nutrition or diet, the food material is enclosed in  food vacuoles , which are bounded by  cell membranes . Digestive enzymes are poured into the newly formed vacuole from the surrounding cytoplasm. In the ciliate  Paramecium , where the process has been researched in detail, the digestive vacuoles initially decrease in size and the enclosed particles  aggregate .

Feeding in Protozoan As digestion proceeds, the vacuole increases in size and the contents become progressively acidic, before gradually becoming alkaline near the end of the process. The products of digestion are then absorbed into the surrounding cytoplasm, and the waste material is ejected from the cell anus, or cytoproct . The length of the digestive cycle varies and depends on the species and the diet.

Feeding in Protozoan Paramecium  contains a reservoir of membrane-forming material in discoid vesicles for the purpose of producing food vacuoles. The food vacuoles form at the cytopharynx when the cytopharyngeal membrane and the discoid vesicles fuse. At the cytoproct, where the vacuoles are broken down and the waste material of digestion is ejected, the membrane material is retrieved and returned to the cytopharynx. Thus, the pool of the digestive vacuole membrane is continuously recycled within the cell.

Feeding in Protozoan Food selection While they seem to lack a sensory system, protozoans are capable of food selection. Many of the filter feeders apparently discriminate solely on the basis of size, dictated by the dimensions of the spaces in the membranelle acting as a sieve. Some filter-feeding ciliates, such as the tintinnids , however, are known to be selective and appear to be able to capture or reject items that arrive at the feeding membranelles in the feeding current. Fig : Filter-feeding Ciliates Tintinnids

Feeding in Protozoan Food selection The large ciliate  Stentor , for example, takes ciliates in preference to flagellated cells and algae, and  discrimination  increases as the animal becomes less hungry. Carnivorous species exercise distinct selectivity. Most suctorians feed exclusively on particular ciliate taxa. They are selective feeders and usually do not capture flagellates, amoebae, or their own ciliated swarmers .

Feeding in Protozoan Food selection Evidence suggests that a reaction between chemical compounds on the surface of the prey and the tentacle tip of the suctorian is responsible for feeding selectivity. Amoeboid organisms also display feeding selectivity.  Amoeba proteus , for example, selects the flagellate  Chilomonas paramecium  in preference to  Monas punctum , even when the number of  Monas  in the medium is high. In this case, selection may be based on the digestibility of the prey; the latter is  digested  in 31/2 hours, and the former in 3 to 18 minutes .

Feeding in Protozoan Mixotrophy All protozoans engage in heterotrophy, but not all protozoans are  exclusive  heterotrophs. Those that combine autotrophy (self-sustaining food production from a carbon source and inorganic nitrogen) and heterotrophy (ingesting other organisms to acquire carbon) are known as mixotrophs. Fig : Mixotrophy

Feeding in Protozoan Mixotrophy The degree of mixotrophy in a protozoan varies from complete reliance on the symbiotic alga (or algae) to transitory retention of the plastids of phytoflagellate prey with only a partial dependence on photosynthesis to supplement the cell’s energy balance.

Feeding in Protozoan Mixotrophy For example, many protozoans, including the predatory ciliate  Stentor  and the  heliozoan  Acanthocystis , are capable of forming  ephemeral   symbioses  with the coccoid green alga  Chlorella . The ciliate  Paramecium bursaria  forms longer-lasting symbiosis with  Chlorella  but must nevertheless acquire the alga with each new generation.

Feeding in Protozoan Photosynthesis and plastid acquisition Many coloured (i.e., photosynthetic) protists combine autotrophy with heterotrophy and therefore are mixotrophs. For example, some members of the euglenoid and cryptomonad groups are mixotrophs.

Feeding in Protozoan Photosynthesis and plastid acquisition The mixotrophic members of these groups are commonly called  acetate flagellates because their preferred organic carbon sources are acetates, simple fatty acids, and alcohols. These organisms are able to switch from  carbohydrate-producing photosynthesis when light is available to heterotrophy on acetate and other substrates when light is not available.

Feeding in Protozoan Photosynthesis and plastid acquisition In another form of mixotrophy, the amoebae and ciliates  sequester  only the plastids of their algal prey (rather than a complete algal cell) and use the plastids for photosynthesis. The plastids do not replicate inside the protozoan (as they do in the symbiotic algae), and thus they must be replaced continuously.

Feeding in Protozoan Photosynthesis and plastid acquisition The large marine ciliate  Tontonia appendiculariformis  may contain thousands of plastids that have been derived from a variety of flagellates.  T. appendiculariformis , however, appears to be selective in its choice of prey, deriving plastids only from certain organisms.

Feeding in Protozoan Symbiotic mixotrophy Mixotrophy is a common phenomenon among free-living protozoans, which usually obtain the capability of photosynthesis from symbionts that are acquired with each new generation (i.e., the photosynthetic machinery is not inherited ). Symbiotic mixotrophy, however, is not “true” mixotrophy, since the combined metabolism results from a  consortium  of two symbionts that are otherwise free-living.

Feeding in Protozoan Symbiotic mixotrophy Many of the foraminiferans and radiolarians possess symbiotic  algae . In some foraminiferans and radiolarians several different symbiotic species of algae may live within the protozoan cytoplasm. During the day the endosymbionts are distributed in the pseudopodial network, but at night they are withdrawn close to the main body of the cell or into the shell.

Feeding in Protozoan Symbiotic mixotrophy Many thousands of these algae may exist within a single protozoan , and a significant amount of the products of photosynthesis (e.g., glucose, alanine, maltose) are transferred from the algae to the protozoan. Indeed, in some circumstances, the protozoan can survive on this source of energy if deprived of food, although its growth may be impaired.

Feeding in Protozoan Mixotrophy in planktonic protozoans Some mixotrophs (e.g., the planktonic protozoans  Dinobryon  and  Ochromonas ) also feed on  bacteria  but are phototrophs first and foremost . Thus, they are “true” mixotrophs, unlike protozoans that  exploit  the photosynthetic capability of symbiotic organisms and cannot carry out this form of metabolism themselves.

Feeding in Protozoan Mixotrophy in planktonic protozoans Many planktonic marine and freshwater mixotrophs feed voraciously on bacteria . In some lakes these protists may be the main consumers of bacteria suspended in surface waters.

Feeding in Protozoan Mixotrophy in planktonic protozoans It is believed that this ingestion of bacteria provides the mixotrophs not only with an additional source of carbon to supplement what is gained by photosynthesis but also with  phosphorus and nitrogen, which are often scarce in biologically productive waters, and possibly with vitamins, which are essential to photosynthesis.

Feeding in Protozoan Mixotrophy in planktonic protozoans Bacteria are more efficient at taking up these nutrients because they have a higher surface-to-volume ratio than protists. Thus, one way for the protists to acquire essential nutrients is to consume the bacteria.