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Nicotiana benthamiana

Nicotiana benthamiana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Nicotiana benthamiana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440414cf0750737592928
Scientific name Nicotiana benthamiana
Authority Domin
First published in Biblioth. Bot. 89: 591. 1929

Description Top

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Nicotiana benthamiana, also known as benth or benthi, is a plant species native to Australia and closely related to tobacco. It was traditionally used by indigenous Australians as a stimulant before the introduction of commercial tobacco. This plant has been used in various research studies, particularly in the fields of plant virology and biotechnology. It is also commonly used for "pharming" monoclonal antibodies and other recombinant proteins. In 2022, a genetically engineered N. benthamiana was developed that could produce 25% of the amount of cocaine found in a coca plant. Additionally, this plant has been used in the development of a COVID-19 vaccine, with Health Canada authorizing its use in February 2022.

Synonyms Top

Scientific name Authority First published in
Nicotiana suaveolens var. cordifolia Benth. Flora Australiensis 4 1868

Common names Top

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Language Common/alternative name
Arabic تبغ بنثاميانا
Catalan n. benthamiana
Persian نیکوتیان
Hebrew ניקוטיאנה
Japanese ベンサミアナタバコ
Macedonian Бентамов тутун
Thai ยาสูบใบเล็ก
Chinese 圓葉菸草
Chinese 本氏烟草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001023691
Tropicos 29600183
KEW urn:lsid:ipni.org:names:816868-1
Open Tree Of Life 1020638
NCBI Taxonomy 4100
IPNI 92803-3
GBIF 3800423
Freebase /m/097r9w
EPPO NIOBE
Elurikkus 416661
USDA GRIN 25258
Wikipedia Nicotiana_benthamiana

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_034376525.1 ASM3437652v1 Chromosome Korea Research Institute of Bioscience and Biotechnology 2023-12-18 55.0x 2.60 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
Characterization of the small Arabidopsis thaliana GTPase and ADP-ribosylation factor-like 2 protein TITAN 5 Mohr I, Mirzaiebadizi A, Sanyal SK, Chuenban P, Ahmadian MR, Ivanov R, Bauer P bioRxiv 27-May-2024
PMCID:PMC10168340
doi:10.1101/2023.04.27.538563
PMID:37162876
‘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
Comparative genomic analyses provide insight into the pathogenicity of three Pseudomonas syringae pv. actinidiae strains from Anhui Province, China Wang Q, Zhang Y, Chen R, Zhang L, Fu M, Zhang L BMC Genomics 11-May-2024
PMCID:PMC11088785
doi:10.1186/s12864-024-10384-1
PMID:38734623
The translocation of a chloride channel from the Golgi to the plasma membrane helps plants adapt to salt stress Rajappa S, Krishnamurthy P, Huang H, Yu D, Friml J, Xu J, Kumar PP Nat Commun 10-May-2024
PMCID:PMC11087495
doi:10.1038/s41467-024-48234-z
PMID:38729926
Intricate Metabolic Network for Paclitaxel Biosynthesis Gou Y, Jiang X, Lian J Biodes Res 09-May-2024
PMCID:PMC11079447
doi:10.34133/bdr.0035
PMID:38725579
A quantitative gibberellin signaling biosensor reveals a role for gibberellins in internode specification at the shoot apical meristem Shi B, Felipo-Benavent A, Cerutti G, Galvan-Ampudia C, Jilli L, Brunoud G, Mutterer J, Vallet E, Sakvarelidze-Achard L, Davière JM, Navarro-Galiano A, Walia A, Lazary S, Legrand J, Weinstain R, Jones AM, Prat S, Achard P, Vernoux T Nat Commun 08-May-2024
PMCID:PMC11079023
doi:10.1038/s41467-024-48116-4
PMID:38719832
Cloning and functional verification of the CmHSP17.9 gene from chrysanthemum Ling Q, Zhang S, Li X, Tang B, Chen A, Zeng T, Ma Q, Chen Y, Tang S, Pan Y, Liu Q, Jia Y, Yong X, Jiang B PLoS One 08-May-2024
PMCID:PMC11078346
doi:10.1371/journal.pone.0301721
PMID:38718030
Functional analysis of the mating type genes in Verticillium dahliae Zhang YD, Ji XB, Zong J, Dai XF, Klosterman SJ, Subbarao KV, Zhang DD, Chen JY BMC Biol 07-May-2024
PMCID:PMC11077750
doi:10.1186/s12915-024-01900-6
PMID:38714997
Elucidating the callus-to-shoot-forming mechanism in Capsicum annuum ‘Dempsey’ through comparative transcriptome analyses Han SY, Park SY, Won KH, Park SI, Park JH, Shim D, Hwang I, Jeong DH, Kim H BMC Plant Biol 07-May-2024
PMCID:PMC11075324
doi:10.1186/s12870-024-05033-4
PMID:38711041
A high-affinity potassium transporter (MeHKT1) from cassava (Manihot esculenta) negatively regulates the response of transgenic Arabidopsis to salt stress Luo M, Chu J, Wang Y, Chang J, Zhou Y, Jiang X BMC Plant Biol 07-May-2024
PMCID:PMC11075273
doi:10.1186/s12870-024-05084-7
PMID:38714917
OsCAMTA3 Negatively Regulates Disease Resistance to Magnaporthe oryzae by Associating with OsCAMTAPL in Rice Yu S, Li S, Wang W, Tang D Int J Mol Sci 06-May-2024
PMCID:PMC11084498
doi:10.3390/ijms25095049
PMID:38732268
Arabidopsis α-Aurora kinase plays a role in cytokinesis through regulating MAP65-3 association with microtubules at phragmoplast midzone Deng X, Xiao Y, Tang X, Liu B, Lin H Nat Commun 06-May-2024
PMCID:PMC11074315
doi:10.1038/s41467-024-48238-9
PMID:38710684
Arabidopsis SBT5.2 and SBT1.7 subtilases mediate C-terminal cleavage of flg22 epitope from bacterial flagellin Matsui S, Noda S, Kuwata K, Nomoto M, Tada Y, Shinohara H, Matsubayashi Y Nat Commun 04-May-2024
PMCID:PMC11069567
doi:10.1038/s41467-024-48108-4
PMID:38704378
Identification of Phytophthora cinnamomi CRN effectors and their roles in manipulating cell death during Persea americana infection Midgley KA, van den Berg N, Backer R, Swart V BMC Genomics 02-May-2024
PMCID:PMC11064341
doi:10.1186/s12864-024-10358-3
PMID:38698341
DELLA proteins recruit the Mediator complex subunit MED15 to coactivate transcription in land plants Hernández-García J, Serrano-Mislata A, Lozano-Quiles M, Úrbez C, Nohales MA, Blanco-Touriñán N, Peng H, Ledesma-Amaro R, Blázquez MA Proc Natl Acad Sci U S A 02-May-2024
PMCID:PMC11087773
doi:10.1073/pnas.2319163121
PMID:38696472

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(3S,5R,10S,13R,14R,17R)-10,13,14-trimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 162818426 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4)O)C)C)C 400.70 unknown https://doi.org/10.1093/JXB/ERG184
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1093/JXB/ERG184
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8S,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 162953289 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1093/JXB/ERG184
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1093/JXB/ERG184
Cycloeucalenol 101690 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C 426.70 unknown https://doi.org/10.1093/JXB/ERG184
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,10S,13R,17R)-4,10,13-trimethyl-17-(6-methyl-5-methylideneheptan-2-yl)-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 5319628 Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCC(=C)C(C)C)C)C)O 412.70 unknown https://doi.org/10.1093/JXB/ERG184
(3S,4S,5R,10S,13R,14R,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-4,10,13,14-tetramethyl-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 162850726 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCC(C)C(C)C)C)C 428.70 unknown https://doi.org/10.1093/JXB/ERG184
(3S,5R,10S,13R,14R,17R)-10,13,14-trimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 162958530 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4)O)C)C)C 412.70 unknown https://doi.org/10.1093/JXB/ERG184
(3S,5R,10S,13R,14R,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13,14-trimethyl-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 163029020 Click to see CC(C)C(C)CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4)O)C)C)C 414.70 unknown https://doi.org/10.1093/JXB/ERG184
(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methyl-5-methyleneheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol 134688501 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown https://doi.org/10.1093/JXB/ERG184
24-Methylenelophenol 5283640 Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCC(=C)C(C)C)C)C)O 412.70 unknown https://doi.org/10.1093/JXB/ERG184
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1093/JXB/ERG184
Obtusifoliol 65252 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCC(=C)C(C)C)C)C 426.70 unknown https://doi.org/10.1093/JXB/ERG184
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,10S,13R)-10,13-Dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 23724574 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1093/JXB/ERG184
(3S,4S,5R,10S,13R,14R,17R)-4,10,13,14-tetramethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 163019902 Click to see CC=C(CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4C)O)C)C)C)C(C)C 440.70 unknown https://doi.org/10.1093/JXB/ERG184
(3S,4S,5S,9S,10S,13R,14R,17R)-4,10,13-trimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11875937 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown https://doi.org/10.1093/JXB/ERG184
(3S,5R,9S,10S,13R,14S,17S)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 162951312 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1093/JXB/ERG184
(3S,5S,10S,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13,14-trimethyl-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 163103978 Click to see CCC(CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4)O)C)C)C)C(C)C 428.70 unknown https://doi.org/10.1093/JXB/ERG184
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1093/JXB/ERG184
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1093/JXB/ERG184
Isofucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1093/JXB/ERG184

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