Details Top

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

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Fresh tuberous root sold as a vegetable in local markets.
- Dried tuberous root ground into flour.
- Starch extracted from roots for industrial uses.
- Seed oil pressed from seeds.
- Seed meal (defatted or whole) used as animal feed.
- Rotenone‑containing seed extract formulated as a natural insecticide.
- Foliage used as livestock forage.

Industrial and craft applications:
- Root starch is employed as a biodegradable film substrate, a binding agent in adhesives, and a fermentation substrate for bio‑ethanol.
- Seed oil serves as a non‑edible industrial oil and as a feedstock for biodiesel production.
- Seed extract containing rotenone is used in botanical insecticide formulations for organic agriculture.

Food and beverages (non‑medicinal):
- Raw tuber sliced or shredded in salads; boiled, roasted, or sautéed in savory dishes.
- Thinly sliced tuber fried to produce crisps or chips.
- Tuber flour incorporated into gluten‑free breads, crackers, and as a thickening agent for soups and sauces.
- Tuber‑based flour has been used in traditional fermented mash preparations, without health claims.

Fragrance and cosmetics:
- Seed oil, rich in linoleic‑type fatty acids, is used as an emollient in cosmetic creams and lotions.

Properties relevant to use:
- Root starch contains a relatively high proportion of amylose (≈30–40 % of total starch), giving high viscosity and good film‑forming ability; gelatinization occurs at modest temperatures (≈65–70 °C).
- Seeds contain ∼20 % protein and ∼15–20 % oil; the oil is dominated by linoleic (≈55 %) and oleic (≈25 %) acids, providing oxidative stability.
- Rotenone concentration in seeds is reported at 0.5–2 % of dry weight, conferring insecticidal activity through inhibition of mitochondrial electron transport.
- As a legume, the plant fixes symbiotic nitrogen, contributing ∼30–50 kg N ha⁻¹ per crop cycle.

Standards and regulation:
- Fresh tuber and derived starch comply with Codex Alimentarius standards for vegetable products (CXS 193‑1995) and for starches; national food regulations (e.g., USDA‑FSA, EU Regulation 1169/2011) apply to commercial distribution.
- Rotenone extracts are registered as botanical pesticides in several jurisdictions (US EPA, EU Plant Protection Products Regulation), with prescribed residue limits and labeling requirements.

Sustainability and sourcing:
- Grown on marginal soils with minimal fertilizer input; nitrogen fixation reduces the need for synthetic N fertilizers.
- Short growth cycle (≈3–4 months) permits multiple cropping seasons per year, enhancing land‑use efficiency.
- Low pesticide reliance due to natural rotenone content; harvested roots and seeds are processed locally, supporting small‑holder livelihoods.

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)
Cacara tuberosa (Lam.) Britton & Wilson

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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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-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!
You can also contribute to this by clicking here.
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-O-glucuronide 5319484 Click to see 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown via CMAUP database
Linarin 5317025 Click to see 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 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 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 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 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 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 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 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 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 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 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 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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