Shreevats Mor, D. Jo Heuschele, Sima Saeidy, Baraem P. Ismail
{"title":"Unlocking Alfalfa’s Potential as a Viable Source of Protein: Improving Protein Extraction and Characterizing the Isolated Protein","authors":"Shreevats Mor, D. Jo Heuschele, Sima Saeidy, Baraem P. Ismail","doi":"10.1021/acsfoodscitech.6c00462","DOIUrl":null,"url":null,"abstract":"<p>Alfalfa (<em>Medicago sativa</em>) stands out among other\r\ngreen biomass for its environmental advantages and potential as a\r\nnovel plant protein source. However, the high extent of proteolysis\r\npost-harvest due to endogenous proteases limits the feasible production\r\nof functional alfalfa protein ingredients. This study aimed to provide\r\na comprehensive evaluation of the structural and functional properties\r\nof alfalfa protein, as impacted by protease inactivation, extraction\r\nconditions, and inherent differences in plant parts across two harvests.\r\nProtein extraction from alfalfa total herbage was significantly enhanced\r\n(<em>P</em> < 0.05) from 37 to 45% when double (15 min)\r\nsolubilization at pH 7 was performed, where the second solubilization\r\nwith fresh solvent (water) led to additional protein recovery. Protein\r\npolymerization, caused by the acid/thermal inactivation of proteases,\r\nhindered any further enhancement in protein extraction yield. Results\r\ndemonstrated that protein extractability from alfalfa leaves was significantly\r\nhigher than from stems. Regardless, the protease inactivation treatment\r\nresulted in protein denaturation and extensive polymerization that\r\nled to poor protein solubility across all alfalfa protein samples.\r\nIn contrast, polymerization and intermolecular β-sheet contributed\r\nto strong gelation properties, namely of the protein isolated from\r\nleaf and total herbage, outperforming both commercial soy and pea\r\nprotein isolates by forming strong gels at lower protein concentration\r\n(10% protein vs 15% and 20%, respectively). These results not only\r\nhighlighted the potential of alfalfa as a source of functional protein\r\nbut also emphasized the need to inactivate proteases while maintaining\r\nthe integrity of the protein.</p>","PeriodicalId":72048,"journal":{"name":"ACS food science & technology","volume":"6 8","pages":"2525–2538"},"PeriodicalIF":3.0000,"publicationDate":"2026-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS food science & technology","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsfoodscitech.6c00462","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/7/17 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"FOOD SCIENCE & TECHNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Alfalfa (Medicago sativa) stands out among other
green biomass for its environmental advantages and potential as a
novel plant protein source. However, the high extent of proteolysis
post-harvest due to endogenous proteases limits the feasible production
of functional alfalfa protein ingredients. This study aimed to provide
a comprehensive evaluation of the structural and functional properties
of alfalfa protein, as impacted by protease inactivation, extraction
conditions, and inherent differences in plant parts across two harvests.
Protein extraction from alfalfa total herbage was significantly enhanced
(P < 0.05) from 37 to 45% when double (15 min)
solubilization at pH 7 was performed, where the second solubilization
with fresh solvent (water) led to additional protein recovery. Protein
polymerization, caused by the acid/thermal inactivation of proteases,
hindered any further enhancement in protein extraction yield. Results
demonstrated that protein extractability from alfalfa leaves was significantly
higher than from stems. Regardless, the protease inactivation treatment
resulted in protein denaturation and extensive polymerization that
led to poor protein solubility across all alfalfa protein samples.
In contrast, polymerization and intermolecular β-sheet contributed
to strong gelation properties, namely of the protein isolated from
leaf and total herbage, outperforming both commercial soy and pea
protein isolates by forming strong gels at lower protein concentration
(10% protein vs 15% and 20%, respectively). These results not only
highlighted the potential of alfalfa as a source of functional protein
but also emphasized the need to inactivate proteases while maintaining
the integrity of the protein.