Nicotiana attenuata - Unknown
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Internal ID UUID6440414ca8148284273613
Scientific name Nicotiana attenuata
Authority Torr. ex S.Watson
First published in Botany [Fortieth Parallel] 276 (t. 27). 1871 [Sep-Dec 1871]

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Synonyms Top

Scientific name Authority First published in
Nicotiana torreyana A.Nelson & J.F.Macbr. Bot. Gaz. 61: 43. 1916

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Language Common/alternative name
English coyote tobacco
Arabic تبغ هزيل
Greek Νικοτιανή η λεπτυσμένη
Korean 니코티아나 아테뉴아타
nv dlǫ́ʼii nátʼoh

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001023679
Canadensys 9358
USDA Plants NIAT
KEW urn:lsid:ipni.org:names:816860-1
Open Tree Of Life 882065
Observations.org 371131
NCBI Taxonomy 49451
Nature Serve 2.149397
iNaturalist 59034
GBIF 2928765
Freebase /m/09gdrfw
EPPO NIOAT
Elurikkus 336465
Calflora (Californian flora) 5857
US Library of Congress sh2004009767
USDA GRIN 102419
Wikipedia Nicotiana_attenuata
IPNI 816860-1

Genomes (via NCBI) Top

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Accession Assembly
Name Level Submitter Released Coverage Size
GCF_001879085.1 NIATTr2 Chromosome Max Planck Institute for Chemical Ecology 2016-11-15 30.0x 2.20 Gb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
‘Candidatus Phytoplasma mali’ SAP11-Like protein modulates expression of genes involved in energy production, photosynthesis, and defense in Nicotiana occidentalis leaves Mittelberger C, Moser M, Hause B, Janik K BMC Plant Biol 13-May-2024
PMCID:PMC11089699
doi:10.1186/s12870-024-05087-4
PMID:38741080
Induced resistance to herbivory and the intelligent plant Kessler A, Mueller MB Plant Signal Behav 30-Apr-2024
PMCID:PMC11062368
doi:10.1080/15592324.2024.2345985
PMID:38687704
Impacts of continuous cropping on the rhizospheric and endospheric microbial communities and root exudates of Astragalus mongholicus Zhou Q, Wang Y, Yue L, Ye A, Xie X, Zhang M, Tian Y, Liu Y, Turatsinze AN, Constantine U, Zhao X, Zhang Y, Wang R BMC Plant Biol 26-Apr-2024
PMCID:PMC11047024
doi:10.1186/s12870-024-05024-5
PMID:38671402
Combining association with linkage mapping to dissect the phenolamides metabolism of the maize kernel Deng M, Zeng Q, Liu S, Jin M, Luo H, Luo J Front Plant Sci 12-Apr-2024
PMCID:PMC11047430
doi:10.3389/fpls.2024.1376405
PMID:38681218
Genome-Wide Identification and Expression Analysis of TGA Family Genes Associated with Abiotic Stress in Sunflowers (Helianthus annuus L.) Zeng Q, Gu J, Cai M, Wang Y, Xie Q, Han Y, Zhang S, Lu L, Chen Y, Zeng Y, Chen T Int J Mol Sci 07-Apr-2024
PMCID:PMC11012525
doi:10.3390/ijms25074097
PMID:38612905
Function and regulation of plant ARGONAUTE proteins in response to environmental challenges: a review Zaheer U, Munir F, Salum YM, He W PeerJ 26-Mar-2024
PMCID:PMC10979746
doi:10.7717/peerj.17115
PMID:38560454
A fungal core effector exploits the OsPUX8B.2–OsCDC48-6 module to suppress plant immunity Shi X, Xie X, Guo Y, Zhang J, Gong Z, Zhang K, Mei J, Xia X, Xia H, Ning N, Xiao Y, Yang Q, Wang GL, Liu W Nat Commun 22-Mar-2024
PMCID:PMC10959940
doi:10.1038/s41467-024-46903-7
PMID:38519521
Comparative transcriptome analysis reveals nicotine metabolism is a critical component for enhancing stress response intensity of innate immunity system in tobacco Song Z, Wang R, Zhang H, Tong Z, Yuan C, Li Y, Huang C, Zhao L, Wang Y, Di Y, Sui X Front Plant Sci 21-Mar-2024
PMCID:PMC11003474
doi:10.3389/fpls.2024.1338169
PMID:38595766
Trading acyls and swapping sugars: metabolic innovations in Solanum trichomes Fiesel PD, Kerwin RE, Daniel Jones A, Last RL bioRxiv 19-Mar-2024
PMCID:PMC10274652
doi:10.1101/2023.06.05.542877
PMID:37333341
Comprehensive analysis of MAPK gene family in upland cotton (Gossypium hirsutum) and functional characterization of GhMPK31 in regulating defense response to insect infestation Wang F, Liang S, Wang G, Wang Q, Xu Z, Li B, Fu C, Fan Y, Hu T, Alariqi M, Hussain A, Cao J, Li J, Zhang X, Jin S Plant Cell Rep 18-Mar-2024
PMCID:PMC10948490
doi:10.1007/s00299-024-03167-1
PMID:38499710
Biochemical characterization of the meiosis-essential yet evolutionarily divergent topoisomerase VIB-like protein MTOPVIB from Arabidopsis thaliana Chen HW, Yeh HY, Chang CC, Kuo WC, Lin SW, Vrielynck N, Grelon M, Chan NL, Chi P Nucleic Acids Res 18-Mar-2024
PMCID:PMC11077084
doi:10.1093/nar/gkae181
PMID:38499490
Improvement of Panax notoginseng saponin accumulation triggered by methyl jasmonate under arbuscular mycorrhizal fungi Dai HY, Zhang XK, Bi Y, Chen D, Long XN, Wu Y, Cao GH, He S Front Plant Sci 13-Mar-2024
PMCID:PMC10965624
doi:10.3389/fpls.2024.1360919
PMID:38545393
A pooled‐sample draft genome assembly provides insights into host plant‐specific transcriptional responses of a Solanaceae‐specializing pest, Tupiocoris notatus (Hemiptera: Miridae) Goldberg JK, Allan CW, Copetti D, Matzkin LM, Bronstein J Ecol Evol 11-Mar-2024
PMCID:PMC10928254
doi:10.1002/ece3.10979
PMID:38476697
Current perspectives on the regulatory mechanisms of sucrose accumulation in sugarcane Mehdi F, Galani S, Wickramasinghe KP, Zhao P, Lu X, Lin X, Xu C, Liu H, Li X, Liu X Heliyon 28-Feb-2024
PMCID:PMC10923725
doi:10.1016/j.heliyon.2024.e27277
PMID:38463882
Wolfberry genome database: integrated genomic datasets for studying molecular biology Cao YL, Chen YY, Li YL, Li CI, Lin ST, Lee BR, Hsieh CL, Hsiao YY, Fan YF, Luo Q, Zhao JH, Yin Y, An W, Shi ZG, Chow CN, Chang WC, Huang CL, Chang WH, Liu ZJ, Wu WS, Tsai WC Front Plant Sci 20-Feb-2024
PMCID:PMC10912414
doi:10.3389/fpls.2024.1310346
PMID:38444537

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
3-Piperidin-2-ylpyridine 2181 Click to see C1CCNC(C1)C2=CN=CC=C2 162.23 unknown https://doi.org/10.1016/S0031-9422(00)80751-7
> Alkaloids and derivatives / Yohimbine alkaloids
Reserpine 5770 Click to see COC1C(CC2CN3CCC4=C(C3CC2C1C(=O)OC)NC5=C4C=CC(=C5)OC)OC(=O)C6=CC(=C(C(=C6)OC)OC)OC 608.70 unknown https://doi.org/10.1021/JF1017737
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2Z,6E,10E,14S)-14-(beta-D-Glucopyranosyloxy)-2,6,10,14-tetramethyl-2,6,10,15-hexadecatetraen-1-yl 2-O-beta-D-glucopyranosyl-beta-D-glucopyranoside 73092396 Click to see CC(=CCCC(=CCCC(C)(C=C)OC1C(C(C(C(O1)CO)O)O)O)C)CCC=C(C)COC2C(C(C(C(O2)CO)O)O)OC3C(C(C(C(O3)CO)O)O)O 792.90 unknown https://doi.org/10.1515/ZNB-2006-0913
2-[4,5-Dihydroxy-2-(hydroxymethyl)-6-[3,7,11,15-tetramethyl-16-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexadeca-1,6,10,14-tetraen-3-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 78052369 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC(C)(CCC=C(C)CCC=C(C)CCC=C(C)COC3C(C(C(C(O3)CO)O)O)O)C=C)CO)O)O)O 776.90 unknown https://doi.org/10.1515/ZNB-2006-0913
2-[6-[16-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 73240539 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC(C)(CCC=C(C)CCC=C(C)CCC=C(C)COC3C(C(C(C(O3)CO)O)O)OC4C(C(C(C(O4)CO)O)O)O)C=C)CO)O)O)O 939.00 unknown https://doi.org/10.1515/ZNB-2006-0913
Attenoside 16091058 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC(C)(CCC=C(C)CCC=C(C)CCC=C(C)COC3C(C(C(C(O3)CO)O)O)OC4C(C(C(C(O4)CO)O)O)O)C=C)CO)O)O)O 939.00 unknown https://doi.org/10.1021/JF1017737
https://doi.org/10.1515/ZNB-2006-0913
Lyciumoside II 11765826 Click to see CC(=CCCC(=CCCC(C)(C=C)OC1C(C(C(C(O1)CO)O)O)O)C)CCC=C(C)COC2C(C(C(C(O2)CO)O)O)OC3C(C(C(C(O3)CO)O)O)O 792.90 unknown https://doi.org/10.1515/ZNB-2006-0913
Lyciumoside IV 71296134 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC(C)(CCC=C(C)CCC=C(C)CCC=C(C)COC3C(C(C(C(O3)CO)O)O)O)C=C)CO)O)O)O 776.90 unknown https://doi.org/10.1021/JF1017737
https://doi.org/10.1515/ZNB-2006-0913
nicotianoside I 71296136 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC(C)(CCC=C(C)CCC=C(C)CCC=C(C)COC3C(C(C(C(O3)COC(=O)CC(=O)O)O)O)O)C=C)CO)O)O)O 862.90 unknown https://doi.org/10.1021/JF1017737
nicotianoside II 71296133 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC(C)(CCC=C(C)CCC=C(C)CCC=C(C)COC3C(C(C(C(O3)COC(=O)CC(=O)O)O)O)O)C=C)COC(=O)CC(=O)O)O)O)O 949.00 unknown https://doi.org/10.1021/JF1017737
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
Anatabine 11388 Click to see C1C=CCNC1C2=CN=CC=C2 160.22 unknown https://doi.org/10.1016/S0031-9422(00)80751-7
> Organoheterocyclic compounds / Pyridines and derivatives / Pyrrolidinylpyridines
3-(1-Methylpyrrolidin-2-yl)pyridine 942 Click to see CN1CCCC1C2=CN=CC=C2 162.23 unknown https://doi.org/10.1021/JF1017737
Nicotine 89594 Click to see CN1CCCC1C2=CN=CC=C2 162.23 unknown https://doi.org/10.1016/S0031-9422(00)80751-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1021/JF1017737

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