Lupinus mutabilis - Unknown
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Internal ID UUID643fdf02b767d455599519
Scientific name Lupinus mutabilis
Authority Sweet
First published in Brit. Fl. Gard.2: t. 130 (1826)

Description Top

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Lupinus mutabilis is a species of lupin grown in the Andes, mainly for its edible bean. It is known by many vernacular names, including tarwi, chocho, altramuz, Andean lupin, South American lupin, Peruvian field lupin, and pearl lupin. It is high in protein and fat, and its nutrient-rich seeds are a good source for cooking oil. It has been used as a food by Andean people since ancient times, but its bitter taste has made it relatively unknown outside the Andes. However, modern technology makes it easier to remove the bitter alkaloids, and it is expanding in use as a plant-based protein source. It is an annual plant that can withstand drought and frost, and is grown at altitudes from 800 to 3,000 metres. It is sown with unselected or selected seeds, and can be used in crop rotation with potatoes and cereals. It is resistant to disease, but breeding goals aim for a low alkaloid content.

Synonyms Top

Scientific name Authority First published in
Lupinus mutabilis var. mutabilis Sweet
Lupinus cruckshanksii Hook. Bot. Mag.58: t. 3056 (1831)
Lupinus mutabilis var. roseus Vargas in C.P.Sm. Spec. Lupinorum: 588 (1948)
Lupinus mutabilis var. cruckshanksii (Hook.) D.Don in Sweet R.Sweet, Brit. Fl. Gard.6: t. 203 (1833)
Lupinus mutabilis f. cruckshanksii (Hook.) Voss Vilm. Blumengärtn. ed. 3, 1: 196 (1896)

Common names Top

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Language Common/alternative name
English tarwi
Spanish tarhui
Spanish tarwi
Arabic ترمس طفري
ay tarwi
German andenlupine
German chochos
German anden-lupine
Esperanto andena lupeno
Estonian muutlik lupiin
Finnish tuoksulupiini
French tarwi
French lupin changeant
French lupin andin
French chocho
Icelandic andeslúpína
Japanese ザッショクノボリフジ
Lithuanian andinis lubinas
Polish Łubin zmienny
Polish Łubin indyjski
Quechua tarwi
Quechua tawri
Chinese 南美羽扇豆

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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-0000213497
USDA Plants LUMU8
Tropicos 13037060
KEW urn:lsid:ipni.org:names:504808-1
The Plant List ild-8563
Open Tree Of Life 324961
NCBI Taxonomy 53232
IPNI 504809-1
iNaturalist 447603
GBIF 2964711
Freebase /m/06lbsf
EPPO LUPMU
EOL 703671
Elurikkus 5580
US Library of Congress sh94000095
USDA GRIN 22844
Wikipedia Lupinus_mutabilis

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
New Analytical Approach to Quinolizidine Alkaloids and Their Assumed Biosynthesis Pathways in Lupin Seeds Namdar D, Mulder PP, Ben-Simchon E, Hacham Y, Basheer L, Cohen O, Sternberg M, Shelef O Toxins (Basel) 21-Mar-2024
PMCID:PMC10974633
doi:10.3390/toxins16030163
PMID:38535829
Field study of parasitic contamination of fruits, vegetables and leafy greens in the Ecuadorian Andes González-Ramírez LC, Djabayan-Djibeyan P, Prato JG, García Ríos CA, Carrero JC, Trelis M, Fuentes MV F1000Res 12-Mar-2024
PMCID:PMC10808852
doi:10.12688/f1000research.132957.1
PMID:38273962
Heavy Metal Bioaccumulation in Peruvian Food and Medicinal Products Tejada-Purizaca TR, Garcia-Chevesich PA, Ticona-Quea J, Martínez G, Martínez K, Morales-Paredes L, Romero-Mariscal G, Arenazas-Rodríguez A, Vanzin G, Sharp JO, McCray JE Foods 29-Feb-2024
PMCID:PMC10931273
doi:10.3390/foods13050762
PMID:38472875
Australian Cool-Season Pulse Seed-Borne Virus Research: 1. Alfalfa and Cucumber Mosaic Viruses and Less Important Viruses Jones RA, Congdon BS Viruses 18-Jan-2024
PMCID:PMC10819373
doi:10.3390/v16010144
PMID:38257844
Evaluation of Phytase Impact on In Vitro Protein and Phosphorus Bioaccessibility of Two Lupin Species for Rainbow Trout (Oncorhynchus mykiss) Azcuy RL, Casaretto ME, Márquez L, Hernández AJ, Morales GA Aquac Nutr 03-Jan-2024
PMCID:PMC10781528
doi:10.1155/2024/2697729
PMID:38213755
Identification and Potential Participation of Lipases in Autophagic Body Degradation in Embryonic Axes of Lupin (Lupinus spp.) Germinating Seeds Wleklik K, Stefaniak S, Nuc K, Pietrowska-Borek M, Borek S Int J Mol Sci 20-Dec-2023
PMCID:PMC10779169
doi:10.3390/ijms25010090
PMID:38203260
Lupin as a Source of Bioactive Antioxidant Compounds for Food Products Estivi L, Brandolini A, Gasparini A, Hidalgo A Molecules 10-Nov-2023
PMCID:PMC10673580
doi:10.3390/molecules28227529
PMID:38005249
Compositional Attributes of Blue Lupin (Lupinus angustifolius) Seeds for Selection of High-Protein Cultivars Roman L, Tsochatzis E, Tarin K, Röndahl EM, Ottosen CO, Corredig M J Agric Food Chem 31-Oct-2023
PMCID:PMC10655177
doi:10.1021/acs.jafc.3c04804
PMID:37906270
Optimization and Characterization of Lupin Protein Isolate Obtained Using Alkaline Solubilization-Isoelectric Precipitation Domínguez R, Bermúdez R, Pateiro M, Lucas-González R, Lorenzo JM Foods 23-Oct-2023
PMCID:PMC10606863
doi:10.3390/foods12203875
PMID:37893768
Unveiling the Evidence for the Use of Pulses in Managing Type 2 Diabetes Mellitus: A Scoping Review Thomas DJ, Shafiee M, Nosworthy MG, Lane G, Ramdath DD, Vatanparast H Nutrients 30-Sep-2023
PMCID:PMC10574713
doi:10.3390/nu15194222
PMID:37836506
Modification of the existing maximum residue levels for mefentrifluconazole in various commodities Bellisai G, Bernasconi G, Carrasco Cabrera L, Castellan I, del Aguila M, Ferreira L, Santonja GG, Greco L, Jarrah S, Leuschner R, Perez JM, Miron I, Nave S, Pedersen R, Reich H, Ruocco S, Santos M, Scarlato AP, Theobald A, Tiramani M, Verani A EFSA J 15-Sep-2023
PMCID:PMC10502649
doi:10.2903/j.efsa.2023.8237
PMID:37719918
Nano-Biofertilizer Formulations for Agriculture: A Systematic Review on Recent Advances and Prospective Applications Garg D, Sridhar K, Stephen Inbaraj B, Chawla P, Tripathi M, Sharma M Bioengineering (Basel) 25-Aug-2023
PMCID:PMC10525541
doi:10.3390/bioengineering10091010
PMID:37760112
Analysis of lncRNAs in Lupinus mutabilis (Tarwi) and Their Potential Role in Drought Response Hidalgo M, Ramos C, Zolla G Noncoding RNA 23-Aug-2023
PMCID:PMC10514842
doi:10.3390/ncrna9050048
PMID:37736894
Product safety aspects of plant molecular farming Buyel JF Front Bioeng Biotechnol 08-Aug-2023
PMCID:PMC10442644
doi:10.3389/fbioe.2023.1238917
PMID:37614627
Sugar Starvation Disrupts Lipid Breakdown by Inducing Autophagy in Embryonic Axes of Lupin (Lupinus spp.) Germinating Seeds Borek S, Stefaniak S, Nuc K, Wojtyla Ł, Ratajczak E, Sitkiewicz E, Malinowska A, Świderska B, Wleklik K, Pietrowska-Borek M Int J Mol Sci 21-Jul-2023
PMCID:PMC10380618
doi:10.3390/ijms241411773
PMID:37511532

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 / Lupin alkaloids / Anagyrine-type alkaloids
(+)-Thermopsine 682648 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1021/JF00119A003
Anagyrin 71056954 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1021/JF00119A003
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 163184988 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1021/JF00119A003
(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 6575009 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1021/JF00119A003
(1R,2R,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 92143189 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1021/JF00119A003
https://doi.org/10.1111/J.2042-7158.1998.TB04013.X
13alpha-Hydroxyspartein-2-one 5459919 Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)O 264.36 unknown https://doi.org/10.1111/J.2042-7158.1998.TB04013.X
https://doi.org/10.1021/JF00119A003
17-Oxolupanine 14139904 Click to see C1CCN2C(C1)C3CC(C2=O)C4CCCC(=O)N4C3 262.35 unknown https://doi.org/10.1021/JF00119A003
4-Hydroxylupanine 6427216 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4O 250.38 unknown https://doi.org/10.1021/JF00119A003
6-Phosphogluconic acid tri(cyclohexylammonium) salt, Grade V 16212687 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1021/JF00119A003
https://doi.org/10.1111/J.2042-7158.1998.TB04013.X
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1021/JF00119A003
https://doi.org/10.1111/J.2042-7158.1998.TB04013.X
Sparteine 644020 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1111/J.2042-7158.1998.TB04013.X
https://doi.org/10.1021/JF00119A003
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Gal(a1-6)D-Ido(a1-6)Glc(a1-2b)Psif 132990894 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OC4(C(C(C(O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O 666.60 unknown https://doi.org/10.1016/0889-1575(88)90035-X
Raffinose 439242 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O 504.40 unknown https://doi.org/10.1016/0889-1575(88)90035-X
Stachyose 439531 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OC4(C(C(C(O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O 666.60 unknown https://doi.org/10.1016/0889-1575(88)90035-X
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
Ammodendrine 442625 Click to see CC(=O)N1CCCC(=C1)C2CCCCN2 208.30 unknown https://doi.org/10.1021/JF00119A003
> Organoheterocyclic compounds / Quinolizidines
(1S,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-5-en-4-one 162886558 Click to see C1CCN2CC3CC(C2C1)CN4C3CC(=O)C=C4 246.35 unknown https://doi.org/10.1021/JF00119A003
Multiflorine 6918763 Click to see C1CCN2CC3CC(C2C1)CN4C3CC(=O)C=C4 246.35 unknown https://doi.org/10.1021/JF00119A003
> Organoheterocyclic compounds / Quinolizidines / Quinolizidinones
(2R,10S)-10-prop-2-enyl-7,11-diazatricyclo[7.3.1.02,7]tridecan-6-one 102004777 Click to see C=CCC1C2CC(CN1)C3CCCC(=O)N3C2 234.34 unknown https://doi.org/10.1021/JF00119A003
1,5-Methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one, decahydro-4-(2-propenyl)-, (1S-(1alpha,4alpha,5alpha,11aalpha))- 3080564 Click to see C=CCC1C2CC(CN1)C3CCCC(=O)N3C2 234.34 unknown https://doi.org/10.1021/JF00119A003
Tetrahydrorhombifoline 15511175 Click to see C=CCCN1CC2CC(C1)C3CCCC(=O)N3C2 248.36 unknown https://doi.org/10.1021/JF00119A003
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/0889-1575(88)90035-X
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/0889-1575(88)90035-X
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
5-hydroxy-3-(3-methoxyphenyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163049564 Click to see COC1=CC=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1021/JF980386L
5-hydroxy-3-(3-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 100954757 Click to see COC1=CC=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1021/JF980386L
5-Hydroxy-3-(3-methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163049563 Click to see COC1=CC=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1021/JF980386L
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
5,7-Dihydroxy-3-(3-methoxyphenyl)chromen-4-one 9882262 Click to see COC1=CC=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O 284.26 unknown https://doi.org/10.1021/JF980386L

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