词条 | Dhurrin |
释义 |
| Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 424742148 | ImageFile=Dhurrin.svg | ImageSize=250px | IUPACName=(2S)-2-(4-Hydroxyphenyl)-2-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]acetonitrile | OtherNames=(S)-4-Hydroxymandelnitrile-β-D-glucopyranoside; (S)-(β-D-Glucopyranosyloxy)(4-hydroxyphenyl)acetonitrile |Section1={{Chembox Identifiers | CASNo_Ref = {{cascite|correct|??}} | CASNo=499-20-7 | PubChem=161355 | SMILES=C1=CC(=CC=C1[C@@H](C#N)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | ChemSpiderID = 141737 | InChI = 1/C14H17NO7/c15-5-9(7-1-3-8(17)4-2-7)21-14-13(20)12(19)11(18)10(6-16)22-14/h1-4,9-14,16-20H,6H2/t9-,10-,11-,12+,13-,14-/m1/s1 | InChIKey = NVLTYOJHPBMILU-YOVYLDAJBT | StdInChI_Ref = {{stdinchicite|changed|chemspider}} | StdInChI = 1S/C14H17NO7/c15-5-9(7-1-3-8(17)4-2-7)21-14-13(20)12(19)11(18)10(6-16)22-14/h1-4,9-14,16-20H,6H2/t9-,10-,11-,12+,13-,14-/m1/s1 | StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} | StdInChIKey = NVLTYOJHPBMILU-YOVYLDAJSA-N |Section2={{Chembox Properties | Formula=C14H17NO7 | MolarMass=311.29 g/mol | Appearance= | Density= | MeltingPt= | BoilingPt= | Solubility= |Section3={{Chembox Hazards | MainHazards= | FlashPt= | AutoignitionPt = }} Dhurrin is a cyanogenic glycoside produced in many plants. Discovered in multiple sorghum varieties in 1906 as the culprit of cattle poisoning by hydrogen cyanide, dhurrin is most typically associated with Sorghum bicolor,[1] the organism used for mapping the biosynthesis of dhurrin from tyrosine. Dhurrin's name is derived form the Arabic word for sorghum, transliterated to "Dhura." BiosynthesisRegulation in Sorghum bicolorIn Sorghum bicolor, dhurrin production is regulated at the transcriptional level and varies depending on the plant’s age and available nutrients. Dhurrin content within Sorghum bicolor can be correlated to the amount of mRNA and translated protein of enzymes CYP79A1 and CYP71E1, two membrane bound members of the cytochrome P450 superfamily. While transcription and translation of these two enzymes is relatively higher for the first few days of growth, transcription is greatly reduced past one week of growth. After five weeks of growth, transcription and translation of both enzymes in the leaves becomes undetectable, while stems in said plants maintain the minimal production of both enzymes. With the addition of excess nitrate, transcription of both enzymes increases, though not to the levels seen in early development.[2] The last enzyme in dhurrin synthesis, UGT85B1, is a soluble enzyme which exchanges glucose from UDP-glucose to the aglycone of dhurrin and forms the glycosidic bond. Transgenic synthesisAddition of both CYP79A1 and CYP71E1 into the genomes of Arabidopsis thaliana and Nicotiana tabacum has been shown to be sufficient for Dhurrin production to occur.[3] Both of these enzymes are sufficient and necessary for Dhurrin production, as removal of the CYP79A1 gene from the Sorghum bicolor genome results in plants lacking dhurrin content. This strain could theoretically be used as a safer crop for fodder in arid environments where sorghum is the only available grain. In vitro biosynthesis of dhurrin has been constructed in both microsomes recovered from Sorghum bicolor seedlings and in micelles.[4] ToxicityMammalsMammalian intestines contain multiple glucosidases which efficiently hydrolyze glycosidic bonds. Upon hydrolysis of the glycosidic bond, the aglycone of dhurrin rapidly degrades to form hydrogen cyanide which is then absorbed into the bloodstream. Lethal dosage of dhurrin in humans and other mammals is theoretically high as one molecule of hydrogen cyanide is produced per molecule of dhurrin. Content of dhurrin by mass in sorghum is relatively low with respect to overall plant matter. As such, it would require a human to eat a considerably large amount of raw sorghum before experiencing adverse effects. In arid environments, sorghum is the best option for cereal grain and fodder as it can withstand extreme drought conditions.[5] Animals consuming the raw sorghum as fodder are much more likely to eat an amount that would contain a lethal dosage of dhurrin for their respective species and can result in animal loss due to hydrogen cyanide poisoning. As an insect repellentIn response to external damage to the stem, sorghum varieties can release dhurrin at the damage site. This response has been shown to repel insects as transgenic sorghum made unable to produce dhurrin was heavily favored by herbivorous insects when compared to wild-type sorghum varieties.[6] References1. ^{{cite book|last1=Blyth|first1=Alexander Wynter|title=Poisons: Their Effects and Detection A Manual for the Use of Analytical Chemists and Experts|date=May 13, 2013|publisher=Charles Griffin and Company|location=USA|page=204}} 2. ^{{cite journal|last1=Busk|first1=Peter Kamp|title=Dhurrin Synthesis in Sorghum Is Regulated at the Transcriptional Level and Induced by Nitrogen Fertilization in Older Plants|journal=Plant Physiology|date=July 2002|volume=129|issue=3|pages=1222–1231|pmc=166516|doi=10.1104/pp.000687|pmid=12114576}} 3. ^{{cite journal|last1=Bak|first1=Soren|title=Transgenic Tobacco and Arabidopsis Plants Expressing the Two Multifunctional Sorghum Cytochrome P450 Enzymes, CYP79A1 and CYP71E1, Are Cyanogenic and Accumulate Metabolites Derived from Intermediates in Dhurrin Biosynthesis|journal=Plant Physiology|date=August 2000|volume=123|issue=4|pages=1437–1448|pmc=59100|doi=10.1104/pp.123.4.1437|pmid=10938360}} 4. ^{{cite journal|last1=Kahn|first1=R A|title=Isolation and reconstitution of cytochrome P450ox and in vitro reconstitution of the entire biosynthetic pathway of the cyanogenic glucoside dhurrin from sorghum.|journal=Plant Physiology|date=December 1997|volume=115|issue=4|pages=1661–1670|pmc=158632|doi=10.1104/pp.115.4.1661|pmid=9414567}} 5. ^{{cite journal|last1=Borrell|first1=Andrew K.|title=Drought adaptation of stay-green sorghum is associated with canopy development, leaf anatomy, root growth, and water uptake|journal=Journal of Experimental Botany|date=2014|volume=65|issue=21|pages=6251–6263|url=http://jxb.oxfordjournals.org/content/65/21/6251|doi=10.1093/jxb/eru232|pmid=25381433|pmc=4223986}} 6. ^{{cite journal|last1=Krothapalli|first1=Kartikeya|title=Forward Genetics by Genome Sequencing Reveals That Rapid Cyanide Release Deters Insect Herbivory of Sorghum Bicolor|journal=Genetics|date=October 2013|volume=195|pages=309–318|url=http://www.genetics.org/content/195/2/309.full.pdf+html?sid=39121ec4-c3f7-43f8-a7d0-8e5107d03b40|doi=10.1534/genetics.113.149567|pmid=23893483|pmc=3781961}} 3 : Cyanogenic glycosides|Phenols|Glucosides |
随便看 |
|
开放百科全书收录14589846条英语、德语、日语等多语种百科知识,基本涵盖了大多数领域的百科知识,是一部内容自由、开放的电子版国际百科全书。