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Pachyrhizus tuberosus

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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 UUID643fd81d5861b812176781
Scientific name Pachyrhizus tuberosus
Authority (Lam.) Spreng.
First published in Syst. Veg. ed. 16, 4(2): 281 (1827)

Description Top

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Synonyms Top

Scientific name Authority First published in
Dolichos tuberosus Lam. Encycl.2: 296 (1786)
Stizolobium tuberosum (Lam.) Spreng. Syst. Veg. ed. 16, 3: 252 (1826)
Cacara tuberosa Britton N.L.Britton & P.Wilson, Sci. Surv. Porto Rico & Virgin Islands5: 424 (1924)

Common names Top

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Language Common/alternative name
English ajipo
Arabic لوبيا بصلية درنية
German knollenbohne
Esperanto tuberfabo

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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

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Database ID/link to page
World Flora Online wfo-0000178282
USDA Plants PATU7
Tropicos 13045290
INPN 670776
KEW urn:lsid:ipni.org:names:512027-1
The Plant List ild-24329
PFAF Pachyrhizus tuberosus
Open Tree Of Life 132206
NCBI Taxonomy 205481
IPNI 1159036-2
GBIF 2974678
EPPO PACTU
EOL 641586
USDA GRIN 26290
CMAUP NPO7656

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

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
G-type receptor-like kinase AsNIP43 interacts with rhizobia effector nodulation outer protein P and is required for symbiosis Liu Y, Lin Y, Wei F, Lv Y, Xie F, Chen D, Lin H, Li Y Plant Physiol 11-Jul-2023
PMCID:PMC10517198
doi:10.1093/plphys/kiad318
PMID:37432453
PEBP Signaling Network in Tubers and Tuberous Root Crops Susila H, Purwestri YA Plants (Basel) 06-Jan-2023
PMCID:PMC9865765
doi:10.3390/plants12020264
PMID:36678976
Scrutiny of NolA and NodD1 Regulatory Roles in Symbiotic Compatibility Unveils New Insights into Bradyrhizobium guangxiense CCBAU53363 Interacting with Peanut (Arachis hypogaea) and Mung Bean (Vigna radiata) Shang JY, Zhang P, Jia YW, Lu YN, Wu Y, Ji S, Chen L, Wang ET, Chen WX, Sui XH Microbiol Spectr 08-Dec-2022
PMCID:PMC9927474
doi:10.1128/spectrum.02096-22
PMID:36475917
Structural insights into the RNA interaction with Yam bean Mosaic virus (coat protein) from Pachyrhizus erosus using bioinformatics approach Acharya V, Arutselvan R, Pati K, Rout AK, Dehury B, Chauhan VB, Nedunchezhiyan M PLoS One 22-Jul-2022
PMCID:PMC9307209
doi:10.1371/journal.pone.0270534
PMID:35867657
Varietas Delectat: Exploring Natural Variations in Nitrogen-Fixing Symbiosis Research Wang T, Balla B, Kovács S, Kereszt A Front Plant Sci 11-Apr-2022
PMCID:PMC9037385
doi:10.3389/fpls.2022.856187
PMID:35481136
A Minimal Genetic Passkey to Unlock Many Legume Doors to Root Nodulation by Rhizobia Unay J, Perret X Genes (Basel) 07-May-2020
PMCID:PMC7290934
doi:10.3390/genes11050521
PMID:32392829
Development of biodegradable films based on purple yam starch/chitosan for food application Martins da Costa JC, Lima Miki KS, da Silva Ramos A, Teixeira-Costa BE Heliyon 12-Apr-2020
PMCID:PMC7160431
doi:10.1016/j.heliyon.2020.e03718
PMID:32322716
Modulation of Symbiotic Compatibility by Rhizobial Zinc Starvation Machinery Zhang P, Zhang B, Jiao J, Dai SQ, Chen WX, Tian CF mBio 18-Feb-2020
PMCID:PMC7029138
doi:10.1128/mBio.03193-19
PMID:32071267
Identification of Soybean Genes Whose Expression is Affected by the Ensifer fredii HH103 Effector Protein NopP Wang J, Wang J, Liu C, Ma C, Li C, Zhang Y, Qi Z, Zhu R, Shi Y, Zou J, Li Q, Zhu J, Wen Y, Sun Z, Liu H, Jiang H, Yin Z, Hu Z, Chen Q, Wu X, Xin D Int J Mol Sci 02-Nov-2018
PMCID:PMC6274870
doi:10.3390/ijms19113438
PMID:30400148
Compatibility between Legumes and Rhizobia for the Establishment of a Successful Nitrogen-Fixing Symbiosis Clúa J, Roda C, Zanetti ME, Blanco FA Genes (Basel) 27-Feb-2018
PMCID:PMC5867846
doi:10.3390/genes9030125
PMID:29495432
Determination of the chemical and functional properties of yam bean (Pachyrhizus erosus (L.) Urban) flour for food systems Buckman ES, Oduro I, Plahar WA, Tortoe C Food Sci Nutr 20-Dec-2017
PMCID:PMC5849927
doi:10.1002/fsn3.574
PMID:29564113
Ecotypic differentiation under farmers' selection: Molecular insights into the domestication of Pachyrhizus Rich. ex DC. (Fabaceae) in the Peruvian Andes Delêtre M, Soengas B, Vidaurre PJ, Meneses RI, Delgado Vásquez O, Oré Balbín I, Santayana M, Heider B, Sørensen M Evol Appl 23-Mar-2017
PMCID:PMC5427675
doi:10.1111/eva.12472
PMID:28515782
Secretion systems and signal exchange between nitrogen-fixing rhizobia and legumes Nelson MS, Sadowsky MJ Front Plant Sci 01-Jul-2015
PMCID:PMC4486765
doi:10.3389/fpls.2015.00491
PMID:26191069
Exploring indigenous landscape classification across different dimensions: a case study from the Bolivian Amazon Riu-Bosoms C, Vidal-Amat T, Duane A, Fernandez-Llamazares A, Guèze M, Luz AC, Macía MJ, Paneque-Gálvez J, Reyes-García V Landsc Res 01-Jan-2015
PMCID:PMC4374147
doi:10.1080/01426397.2013.829810
PMID:25821282
Rotenone isolated from Pachyrhizus erosus displays cytotoxicity and genotoxicity in K562 cells. Estrella-Parra EA, Gomez-Verjan JC, González-Sánchez I, Vázquez-Martínez ER, Vergara-Castañeda E, Cerbón MA, Alavez-Solano D, Reyes-Chilpa R Nat Prod Res 01-Jan-2014
doi:10.1080/14786419.2014.939081
PMID:25055205

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
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Apigenin 7-glucuronide 5319484 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
Linarin 5317025 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O 592.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-3-enes / Isoflav-3-enones
6-(2,4,5Trimethoxyphenyl)furo[3,2-g]chromen-7-one 129882389 Click to see COC1=CC(=C(C=C1C2=CC3=C(C=C4C(=C3)C=CO4)OC2=O)OC)OC 352.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
Pachyrrhizin 101277 Click to see COC1=CC2=C(C=C1C3=CC4=C(C=C5C(=C4)C=CO5)OC3=O)OCO2 336.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
https://doi.org/10.1080/14786419.2014.939081
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 2-O-methylated isoflavonoids
(6R)-6-(6-methoxy-1,3-benzodioxol-5-yl)-6,7-dihydrofuro[3,2-g]chromen-5-one 92169662 Click to see COC1=CC2=C(C=C1C3COC4=C(C3=O)C=C5C=COC5=C4)OCO2 338.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
(6S)-6-(6-methoxy-1,3-benzodioxol-5-yl)-6,7-dihydrofuro[3,2-g]chromen-5-one 92147813 Click to see COC1=CC2=C(C=C1C3COC4=C(C3=O)C=C5C=COC5=C4)OCO2 338.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
Neotenone 73603 Click to see COC1=CC2=C(C=C1C3COC4=C(C3=O)C=C5C=COC5=C4)OCO2 338.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(13R)-5,7,11,14,18-pentaoxahexacyclo[11.11.0.02,10.04,8.015,23.017,21]tetracosa-2,4(8),9,15(23),16,19,21-heptaen-24-one 163194463 Click to see C1C2C(C3=CC4=C(C=C3O1)OCO4)C(=O)C5=C(O2)C=C6C(=C5)C=CO6 336.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
(1R,13R)-5,7,11,14,18-pentaoxahexacyclo[11.11.0.02,10.04,8.015,23.017,21]tetracosa-2,4(8),9,15(23),16,19,21-heptaen-24-one 21676231 Click to see C1C2C(C3=CC4=C(C=C3O1)OCO4)C(=O)C5=C(O2)C=C6C(=C5)C=CO6 336.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
(1R,13S)-1-hydroxy-5,7,11,14,18-pentaoxahexacyclo[11.11.0.02,10.04,8.015,23.017,21]tetracosa-2,4(8),9,15(23),16,19,21-heptaen-24-one 13885697 Click to see C1C2C(C3=CC4=C(C=C3O1)OCO4)(C(=O)C5=C(O2)C=C6C(=C5)C=CO6)O 352.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
(1R,13S)-16,17-dimethoxy-2,6,20-trioxapentacyclo[11.8.0.03,11.05,9.014,19]henicosa-3(11),4,7,9,14,16,18-heptaen-12-one 162988993 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C=C5C=COC5=C4)OC 352.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
(1S,13R)-1-hydroxy-5,7,11,14,18-pentaoxahexacyclo[11.11.0.02,10.04,8.015,23.017,21]tetracosa-2,4(8),9,15(23),16,19,21-heptaen-24-one 154495953 Click to see C1C2C(C3=CC4=C(C=C3O1)OCO4)(C(=O)C5=C(O2)C=C6C(=C5)C=CO6)O 352.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
(1S,13R)-5,7,11,14,18-pentaoxahexacyclo[11.11.0.02,10.04,8.015,23.017,21]tetracosa-2,4(8),9,15(23),16,19,21-heptaen-24-one 162908087 Click to see C1C2C(C3=CC4=C(C=C3O1)OCO4)C(=O)C5=C(O2)C=C6C(=C5)C=CO6 336.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
(1S,13S)-16,17-dimethoxy-2,6,20-trioxapentacyclo[11.8.0.03,11.05,9.014,19]henicosa-3(11),4,7,9,14,16,18-heptaen-12-one 154496536 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C=C5C=COC5=C4)OC 352.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
(1S,6S,13R)-16,17-dimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one 7059608 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
12a-Hydroxydolineone 13885696 Click to see C1C2C(C3=CC4=C(C=C3O1)OCO4)(C(=O)C5=C(O2)C=C6C(=C5)C=CO6)O 352.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
5'beta-Rotenone 5102 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1080/14786419.2014.939081
https://doi.org/10.1016/0031-9422(92)83161-Q
Dolineone 5316959 Click to see C1C2C(C3=CC4=C(C=C3O1)OCO4)C(=O)C5=C(O2)C=C6C(=C5)C=CO6 336.30 unknown https://doi.org/10.1080/14786419.2014.939081
https://doi.org/10.1016/0031-9422(92)83161-Q
Epirotenone 7059609 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
Erosone 5317190 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C=C5C=COC5=C4)OC 352.30 unknown https://doi.org/10.1016/0031-9422(92)83161-Q
Rotenone 6758 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1016/0031-9422(92)83161-Q

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