Toxalbumin

Last updated
Ricinus communis Illustration Ricinus communis0.jpg

Toxalbumins are toxic plant proteins that disable ribosomes and thereby inhibit protein synthesis, producing severe cytotoxic effects in multiple organ systems. They are dimers held together by a disulfide bond and comprise a lectin (carbohydrate-binding protein) part which binds to the cell membrane and enables the toxin part to gain access to the cell contents. Toxalbumins are similar in structure to AB toxins found in cholera, tetanus, diphtheria, botulinum and others; [1] and their physiological and toxic properties are similar to those of viperine snake venom.[ citation needed ]

Contents

Toxalbumins were first described in about 1890 by Ludwig Brieger (1849–1919) and Sigmund Fraenkel (1868–1939), associates of the organic chemist Eugen Baumann. Brieger first used the term toxin. [2]

Toxalbumins notably are present in the plant families Leguminosae and Euphorbiaceae, occurring for instance in Robinia pseudoacacia , Abrus precatorius , Jatropha curcas , Croton gratissimus and Ricinus communis . Typical toxalbumins are abrin and ricin. [3] [ self-published source? ] [4] Ingestion of seed containing toxalbumins is not necessarily fatal as the hard seed coat will withstand digestion, unless the seed has been pierced, as would happen in the making of necklaces, prayer beads or bracelets, and even then the toxalbumin is likely to be digested and thereby rendered harmless. Toxalbumins injected intravenously or subcutaneously or inhaled in powdered form, though, are highly toxic. A latent period of hours to days may follow with no sensible signs of distress, after which symptoms of nausea, vomiting and diarrhoea will appear, followed by delirium, seizures, coma, and death. From an evolutionary viewpoint, toxalbumins developed as a deterrent to consumption of seeds, foliage, bark and roots. Ripe fruits having a fleshy pulp are usually tasty and edible and lacking toxalbumins, encourage ingestion and the consequent distribution of seeds that have a coat sufficiently durable to survive a passage through the digestive system of a herbivore or fructivore. [5] [6]

Being soluble in water, ricin is not present in extracted oils. As with most proteins it breaks down after heat treatment, such as cooking or steaming, and after the oil is extracted, the resulting pomace is often used as animal feed. There is an enormous variation in sensitivity to the toxin, and a lethal dose may be as little as two-millionths of body weight. Since ricin is a protein, antibodies may be produced by inoculation, allowing resistance of up to 800 times a normal lethal dose. Ricin has been used in assassinations, a notorious case being the use of a 1.53 mm pellet holding a few hundred millionths of a gram of ricin to kill the Bulgarian broadcaster, Georgi Markov, who died 4 days after being attacked. [7]

Compared to amatoxins

The toxins present in poisonous mushrooms such as Amanita phalloides are quite different from toxalbumins and are mostly secondary metabolites or amatoxins which do not readily break down under applied heat. They are potent inhibitors of RNA polymerase II, an enzyme vital in the synthesis of messenger RNA (mRNA), microRNA, and small nuclear RNA (snRNA). Without mRNA, the template for protein synthesis, cell metabolism stops. In this respect, their metabolic effect is similar to that of toxalbumins.

See also

Related Research Articles

<span class="mw-page-title-main">Toxin</span> Naturally occurring organic poison

A toxin is a naturally occurring organic poison produced by metabolic activities of living cells or organisms. Toxins occur especially as a protein or conjugated protein. The term toxin was first used by organic chemist Ludwig Brieger (1849–1919) and is derived from the word toxic.

<span class="mw-page-title-main">Poison</span> Substance that causes death, injury or harm to organs

Poison is something that causes harm. The term is used in a wide range of scientific fields and industries, where it is often specifically defined. It may also be applied colloquially or figuratively, with a broad sense.

<i>Ricinus</i> Monotypic genus of plant in the family Euphorbiaceae

Ricinus communis, the castor bean or castor oil plant, is a species of perennial flowering plant in the spurge family, Euphorbiaceae. It is the sole species in the monotypic genus, Ricinus, and subtribe, Ricininae. The evolution of castor and its relation to other species are currently being studied using modern genetic tools. It reproduces with a mixed pollination system which favors selfing by geitonogamy but at the same time can be an out-crosser by anemophily or entomophily.

<span class="mw-page-title-main">Ricin</span> Type of toxic lectin

Ricin ( RY-sin) is a lectin (a carbohydrate-binding protein) and a highly potent toxin produced in the seeds of the castor oil plant, Ricinus communis. The median lethal dose (LD50) of ricin for mice is around 22 micrograms per kilogram of body weight via intraperitoneal injection. Oral exposure to ricin is far less toxic. An estimated lethal oral dose in humans is approximately 1 milligram per kilogram of body weight.

<i>Abrus precatorius</i> Species of flowering plant in the bean family Fabaceae

Abrus precatorius, commonly known as jequirity bean or rosary pea, is a herbaceous flowering plant in the bean family Fabaceae. It is a slender, perennial climber with long, pinnate-leafleted leaves that twines around trees, shrubs, and hedges.

<span class="mw-page-title-main">Lectin</span> Carbohydrate-binding protein

Lectins are carbohydrate-binding proteins that are highly specific for sugar groups that are part of other molecules, so cause agglutination of particular cells or precipitation of glycoconjugates and polysaccharides. Lectins have a role in recognition at the cellular and molecular level and play numerous roles in biological recognition phenomena involving cells, carbohydrates, and proteins. Lectins also mediate attachment and binding of bacteria, viruses, and fungi to their intended targets.

<i>Adenia</i> Genus of plants

Adenia is a genus of flowering plants in the passionflower family, Passifloraceae. It is distributed in the Old World tropics and subtropics. The centers of diversity are in Madagascar, eastern and western tropical Africa, and Southeast Asia. The genus name Adenia comes from "aden", reported as the Arabic name for the plant by Peter Forsskål, the author of the genus.

<span class="mw-page-title-main">Cicutoxin</span> Chemical compound

Cicutoxin is a naturally-occurring poisonous chemical compound produced by several plants from the family Apiaceae including water hemlock (Cicuta species) and water dropwort (Oenanthe crocata). The compound contains polyene, polyyne, and alcohol functional groups and is a structural isomer of oenanthotoxin, also found in water dropwort. Both of these belong to the C17-polyacetylenes chemical class.

<span class="mw-page-title-main">Abrin</span> Chemical compound

Abrin is an extremely toxic toxalbumin found in the seeds of the rosary pea, Abrus precatorius. It has a median lethal dose of 0.7 micrograms per kilogram of body mass when given to mice intravenously. The median toxic dose for humans ranges from 10 to 1000 micrograms per kilogram when ingested and is 3.3 micrograms per kilogram when inhaled.

Amatoxin is the collective name of a subgroup of at least nine related toxic compounds found in three genera of poisonous mushrooms and one species of the genus Conocybe. Amatoxins are lethal in even small doses, as little as half a mushroom, including the immature 'egg' form which appears quite different from the fully-grown mushroom.

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

The trichothecenes are a large family of chemically related mycotoxins. They are produced by various species of Fusarium, Myrothecium, Trichoderma/Podostroma, Trichothecium, Cephalosporium, Verticimonosporium, and Stachybotrys. Chemically, trichothecenes are a class of sesquiterpenes.

Phytotoxins are substances that are poisonous or toxic to the growth of plants. Phytotoxic substances may result from human activity, as with herbicides, or they may be produced by plants, by microorganisms, or by naturally occurring chemical reactions.

Saporin is a protein that is useful in biological research applications, especially studies of behavior. Saporin is a so-called ribosome inactivating protein (RIP), due to its N-glycosidase activity, from the seeds of Saponaria officinalis. It was first described by Fiorenzo Stirpe and his colleagues in 1983 in an article that illustrated the unusual stability of the protein.

Peter Hermann Stillmark was a Baltic-German microbiologist.

<span class="mw-page-title-main">Ribosome-inactivating protein</span> Protein synthesis inhibitor

A ribosome-inactivating protein (RIP) is a protein synthesis inhibitor that acts at the eukaryotic ribosome. This protein family describes a large family of such proteins that work by acting as rRNA N-glycosylase. They inactivate 60S ribosomal subunits by an N-glycosidic cleavage, which releases a specific adenine base from the sugar-phosphate backbone of 28S rRNA. RIPs exist in bacteria and plants.

<span class="mw-page-title-main">Ricinine</span> Chemical compound

Ricinine is a toxic alkaloid found in the castor plant. It can serve as a biomarker of ricin poisoning. It was first isolated from the castor seeds by Tuson in 1864.

Volkensin is a eukaryotic ribosome-inactivating protein found in the Adenia volkensii plant. It is a glycoprotein with two subunits A and B. A subunit is linked to B subunit with disulfide bridges and non-covalent bonds. B subunit is responsible for binding to the galactosyl-terminated receptors on the cell membrane that allows the entry the A subunit of the toxin into the cell, which performs the inhibitory function. Volkensin is a galactose specific lectin that can inhibit protein synthesis in whole cells and in cell-free lysates. This protein can be included into the category of risin like toxins and it resembles modeccin, the toxin of Adenia digitata. Although very similar in composition, volkensin contains more cysteine residues and more than twice as much sugar than modeccin, due to high content of galactose and mannose. In addition, volkensin is able to inhibit protein synthesis at concentrations 10 times lower than required for modeccin. From gene sequencing analysis, volkensin was found to be coded by 1569-bp ORF, that is 523 amino acid residues without introns. The internal linker sequence is 45 bp. The active site of the A subunit contains Ser203, a novel residue that is conserved in all ribosome inactivating proteins.

Modeccin is a toxic lectin, a group of glycoproteins capable of binding specifically to sugar moieties. Different toxic lectins are present in seeds of different origin. Modeccin is found in the roots of the African plant Adenia digitata. These roots are often mistaken for edible roots, which has led to some cases of intoxication. Sometimes the fruit is eaten, or a root extract is drunk as a manner of suicide.

<span class="mw-page-title-main">Substances poisonous to dogs</span> Harmful substances

There are a wide variety of substances poisonous to dogs. Many pet owners have a general knowledge of dog health, but not of the larger scope of common substances poisonous to dogs. Recognizing the signs of poisoning will enable dog owners to get the help their dogs need when exposed to poisons. Dogs can be exposed to poisons in several ways: ingestion, contact, and inhalation. The most common poisonous substances include some human foods and medications, household products, and many plants. Understanding exposure and symptoms of poisoning and poisonous substances will assist dog owners in identifying how to get the correct treatment for their pet.

References

  1. Hunter, William (1891). "On the Nature, Action, and Therapeutic Value of the Active Principles of Tuberculin". British Medical Journal. 2 (1595): 169–76. doi:10.1136/bmj.2.1595.169. JSTOR   20243302. PMC   2273336 . PMID   20753375.
  2. Rietschel, Ernst T.; Westphal, Otto (1999). "Endotoxin: Historical Perspectives". In Brade, Helmut (ed.). Endotoxin in Health and Disease. CRC. pp. 1–30. ISBN   978-0-8247-1944-9.
  3. "Toxalbumins – Peas and beans gone bad". Drugs and Poisons. 2004-02-26. Retrieved 2015-06-16.
  4. Brent, Jeffrey (2005). Critical Care Toxicology: Diagnosis and Management of the Critically Poisoned Patient. Mosby. p. 1345. ISBN   978-0-8151-4387-1.
  5. Medicinal and Poisonous Plants of Southern and Eastern Africa – John Mitchell Watt, Maria Gerdina Breyer-Brandwijk (E. & S. Livingstone Ltd. (1962))[ page needed ]
  6. Castor Bean and Jequirity Bean Poisoning at eMedicine
  7. "Castor-bean". Canadian Poisonous Plants Information System. Canadian Biodiversity Information Facility. April 11, 2014.