Appendage

Last updated
A beetle leg Procerus middle leg.jpg
A beetle leg

An appendage (or outgrowth) is an external body part, or natural prolongation, that protrudes from an organism's or microorganism's body.

Contents

Types in animals

In arthropods, an appendage refers to any of the homologous body parts that may extend from a body segment, including antennae, mouthparts (including mandibles, maxillae and maxillipeds), gills, locomotor legs (pereiopods for walking, and pleopods for swimming), sexual organs (gonopods), and parts of the tail (uropods). Typically, each body segment carries one pair of appendages. An appendage which is modified to assist in feeding is known as a maxilliped or gnathopod.[ citation needed ]

In vertebrates, an appendage can refer to a locomotor part such as a tail, fins on a fish, limbs (arms, legs, flippers or wings) on a tetrapod; exposed sex organ; defensive parts such as horns and antlers; or sensory organs such as auricles, proboscis (trunk and snout) and barbels.[ citation needed ]

Appendages may become uniramous, as in insects and centipedes, where each appendage comprises a single series of segments, or it may be biramous, as in many crustaceans, where each appendage branches into two sections. Triramous (branching into three) appendages are also possible. [1]

All arthropod appendages are variations of the same basic structure (homologous), and which structure is produced is controlled by "homeobox" genes. Changes to these genes have allowed scientists to produce animals (chiefly Drosophila melanogaster ) with modified appendages, such as legs instead of antennae. [2]

Types in prokaryotes

A number of cell surface appendages are found in prokaryotesbacteria and archaea, and include flagella, pili, and prosthecae also called stalks.

Archaea

A number of surface appendages may be present on different archaea. Two types of appendage are species-specific; cannulae are specific to Pyrodictium species, and hami are specific to Altiarchaeum. [3] Other various types of surface structure include pili, archaella (archaeal flagella), structures called bindisomes that bind sugars, and posttranslationally modified archaellins and pilins. [4] [5]

Archaella are the similar structures to bacterial flagella with the same function in motility particularly swimming, but with a different composition and action. Pili are used in attachment to surfaces, possible communication between cells enabling cell to cell contact allowing genetic transfer, and the formation of biofilms. [4] A type IV pili model is used in the assembly of several cell surface structures. The bindisome is made up of sugar binding proteins to facilitate sugar uptake. So far studies are limited to S. solfataricus. [4] Appendage fibres described as Iho670 fibres are unique to Ignicoccus hospitalis . [4]

Bacteria

Bacterial surface appendages include flagella, pili, short attachment pili known as fimbriae, and on some species curli fibres. Some bacteria also have stalks known as prosthecae.

Types in plants

A leaf is the main appendage of a plant stem. Prosthechea is a genus of orchids named for the prostheca appendage on the back of the column. Hair like structures known as trichomes are found on many types of plants.

Related Research Articles

<span class="mw-page-title-main">Pilus</span> A proteinaceous hair-like appendage on the surface of bacteria

A pilus is a hair-like appendage found on the surface of many bacteria and archaea. The terms pilus and fimbria can be used interchangeably, although some researchers reserve the term pilus for the appendage required for bacterial conjugation. All conjugative pili are primarily composed of pilin – fibrous proteins, which are oligomeric.

<span class="mw-page-title-main">Flagellum</span> Cellular appendage functioning as locomotive or sensory organelle

A flagellum is a hairlike appendage that protrudes from certain plant and animal sperm cells, from fungal spores (zoospores), and from a wide range of microorganisms to provide motility. Many protists with flagella are known as flagellates.

The evolution of flagella is of great interest to biologists because the three known varieties of flagella – each represent a sophisticated cellular structure that requires the interaction of many different systems.

Segmentation in biology is the division of some animal and plant body plans into a linear series of repetitive segments that may or may not be interconnected to each other. This article focuses on the segmentation of animal body plans, specifically using the examples of the taxa Arthropoda, Chordata, and Annelida. These three groups form segments by using a "growth zone" to direct and define the segments. While all three have a generally segmented body plan and use a growth zone, they use different mechanisms for generating this patterning. Even within these groups, different organisms have different mechanisms for segmenting the body. Segmentation of the body plan is important for allowing free movement and development of certain body parts. It also allows for regeneration in specific individuals.

Hox genes, a subset of homeobox genes, are a group of related genes that specify regions of the body plan of an embryo along the head-tail axis of animals. Hox proteins encode and specify the characteristics of 'position', ensuring that the correct structures form in the correct places of the body. For example, Hox genes in insects specify which appendages form on a segment, and Hox genes in vertebrates specify the types and shape of vertebrae that will form. In segmented animals, Hox proteins thus confer segmental or positional identity, but do not form the actual segments themselves.

<span class="mw-page-title-main">Pseudopeptidoglycan</span>

Pseudopeptidoglycan is a major cell wall component of some Archaea that differs from bacterial peptidoglycan in chemical structure, but resembles bacterial peptidoglycan in function and physical structure. Pseudopeptidoglycan, in general, is only present in a few methanogenic archaea. The basic components are N-acetylglucosamine and N-acetyltalosaminuronic acid, which are linked by β-1,3-glycosidic bonds.

The arthropod leg is a form of jointed appendage of arthropods, usually used for walking. Many of the terms used for arthropod leg segments are of Latin origin, and may be confused with terms for bones: coxa, trochanter, femur, tibia, tarsus, ischium, metatarsus, carpus, dactylus, patella.

Microbial genetics is a subject area within microbiology and genetic engineering. Microbial genetics studies microorganisms for different purposes. The microorganisms that are observed are bacteria, and archaea. Some fungi and protozoa are also subjects used to study in this field. The studies of microorganisms involve studies of genotype and expression system. Genotypes are the inherited compositions of an organism. Genetic Engineering is a field of work and study within microbial genetics. The usage of recombinant DNA technology is a process of this work. The process involves creating recombinant DNA molecules through manipulating a DNA sequence. That DNA created is then in contact with a host organism. Cloning is also an example of genetic engineering.

<span class="mw-page-title-main">Sulfolobales</span> Order of archaea

Sulfolobales is an order of archaeans in the class Thermoprotei.

<span class="mw-page-title-main">Sulfolobaceae</span> Family of archaea

Sulfolobaceae are a family of the Sulfolobales belonging to the domain Archaea. The family consists of several genera adapted to survive environmental niches with extreme temperature and low pH conditions.

Icerudivirus is a genus of viruses in the family Rudiviridae. These viruses are non-enveloped, stiff-rod-shaped viruses with linear dsDNA genomes, that infect hyperthermophilic archaea of the species Sulfolobus islandicus. There are three species in the genus.

<i>Lipothrixviridae</i> Family of viruses

Lipothrixviridae is a family of viruses in the order Ligamenvirales. Thermophilic archaea in the phylum Thermoproteota serve as natural hosts. There are 11 species in this family, assigned to 4 genera.

<span class="mw-page-title-main">Bacterial motility</span> Ability of bacteria to move independently using metabolic energy

Bacterial motility is the ability of bacteria to move independently using metabolic energy. Most motility mechanisms that evolved among bacteria also evolved in parallel among the archaea. Most rod-shaped bacteria can move using their own power, which allows colonization of new environments and discovery of new resources for survival. Bacterial movement depends not only on the characteristics of the medium, but also on the use of different appendages to propel. Swarming and swimming movements are both powered by rotating flagella. Whereas swarming is a multicellular 2D movement over a surface and requires the presence of surfactants, swimming is movement of individual cells in liquid environments.

<span class="mw-page-title-main">Archaea</span> Domain of single-celled organisms

Archaea is a domain of single-celled organisms. These microorganisms lack cell nuclei and are therefore prokaryotes. Archaea were initially classified as bacteria, receiving the name archaebacteria, but this term has fallen out of use.

<span class="mw-page-title-main">Sexual reproduction</span> Biological process

Sexual reproduction is a type of reproduction that involves a complex life cycle in which a gamete with a single set of chromosomes combines with another gamete to produce a zygote that develops into an organism composed of cells with two sets of chromosomes (diploid). This is typical in animals, though the number of chromosome sets and how that number changes in sexual reproduction varies, especially among plants, fungi, and other eukaryotes.

The archaellum is a unique structure on the cell surface of many archaea that allows for swimming motility. The archaellum consists of a rigid helical filament that is attached to the cell membrane by a molecular motor. This molecular motor – composed of cytosolic, membrane, and pseudo-periplasmic proteins – is responsible for the assembly of the filament and, once assembled, for its rotation. The rotation of the filament propels archaeal cells in liquid medium, in a manner similar to the propeller of a boat. The bacterial analog of the archaellum is the flagellum, which is also responsible for their swimming motility and can also be compared to a rotating corkscrew. Although the movement of archaella and flagella is sometimes described as "whip-like", this is incorrect, as only cilia from Eukaryotes move in this manner. Indeed, even "flagellum" is a misnomer, as bacterial flagella also work as propeller-like structures.

<span class="mw-page-title-main">Twitching motility</span> Form of crawling bacterial motility

Twitching motility is a form of crawling bacterial motility used to move over surfaces. Twitching is mediated by the activity of hair-like filaments called type IV pili which extend from the cell's exterior, bind to surrounding solid substrates, and retract, pulling the cell forwards in a manner similar to the action of a grappling hook. The name twitching motility is derived from the characteristic jerky and irregular motions of individual cells when viewed under the microscope. It has been observed in many bacterial species, but is most well studied in Pseudomonas aeruginosa, Neisseria gonorrhoeae and Myxococcus xanthus. Active movement mediated by the twitching system has been shown to be an important component of the pathogenic mechanisms of several species.

<span class="mw-page-title-main">Marine prokaryotes</span> Marine bacteria and marine archaea

Marine prokaryotes are marine bacteria and marine archaea. They are defined by their habitat as prokaryotes that live in marine environments, that is, in the saltwater of seas or oceans or the brackish water of coastal estuaries. All cellular life forms can be divided into prokaryotes and eukaryotes. Eukaryotes are organisms whose cells have a nucleus enclosed within membranes, whereas prokaryotes are the organisms that do not have a nucleus enclosed within a membrane. The three-domain system of classifying life adds another division: the prokaryotes are divided into two domains of life, the microscopic bacteria and the microscopic archaea, while everything else, the eukaryotes, become the third domain.

<span class="mw-page-title-main">Archaeal virus</span> Type of virus that infects the domain of unicellular, prokaryotic organisms or Archaea

An archaeal virus is a virus that infects and replicates in archaea, a domain of unicellular, prokaryotic organisms. Archaeal viruses, like their hosts, are found worldwide, including in extreme environments inhospitable to most life such as acidic hot springs, highly saline bodies of water, and at the bottom of the ocean. They have been also found in the human body. The first known archaeal virus was described in 1974 and since then, a large diversity of archaeal viruses have been discovered, many possessing unique characteristics not found in other viruses. Little is known about their biological processes, such as how they replicate, but they are believed to have many independent origins, some of which likely predate the last archaeal common ancestor (LACA).

Archaea, one of the three domains of life, are a highly diverse group of prokaryotes that include a number of extremophiles. One of these extremophiles has given rise to a highly complex new appendage known as the hamus. In contrast to the well-studied prokaryotic appendages pili and fimbriae, much is yet to be discovered about archaeal appendages such as hami. Appendages serve multiple functions for cells and are often involved in attachment, horizontal conjugation, and movement. The unique appendage was discovered at the same time as the unique community of archaea that produces them. Research into the structure of hami suggests their main function aids in attachment and biofilm formation. This is accomplished due to their evenly placed prickles, helical structure, and barbed end. These appendages are heat and acid resistant, aiding in the cell's ability to live in extreme environments.

References

  1. Morris, Simon Conway (1979). "The Burgess Shale (Middle Cambrian) Fauna". Annual Review of Ecology and Systematics. 10: 327–349. doi:10.1146/annurev.es.10.110179.001551. JSTOR   2096795 . Retrieved 17 November 2020.
  2. Emerald, B. Starling; Cohen, Stephen (March 2004). "Spatial and temporal regulation of the homeotic selector gene Antennapedia is required for the establishment of leg identity in Drosophila". Developmental Biology. 267 (2): 462–472. doi:10.1016/j.ydbio.2003.12.006. PMID   15013806.
  3. van Wolferen, M; Pulschen, AA; Baum, B; Gribaldo, S; Albers, SV (November 2022). "The cell biology of archaea". Nature Microbiology. 7 (11): 1744–1755. doi:10.1038/s41564-022-01215-8. PMC   7613921 . PMID   36253512.
  4. 1 2 3 4 Jarrell, KF; Ding, Y; Nair, DB; Siu, S (24 January 2013). "Surface appendages of archaea: structure, function, genetics and assembly". Life. 3 (1): 86–117. Bibcode:2013Life....3...86J. doi: 10.3390/life3010086 . PMC   4187195 . PMID   25371333.
  5. Lassak, K; Ghosh, A; Albers, SV (November 2012). "Diversity, assembly and regulation of archaeal type IV pili-like and non-type-IV pili-like surface structures". Research in Microbiology. 163 (9–10): 630–44. doi: 10.1016/j.resmic.2012.10.024 . PMID   23146836. S2CID   37802794.

See also