Challenges in Using the Official Italian Method to Detect Bovine Whey Proteins in Protected Designation of Origin Buffalo Mozzarella: A Proteomic Approach to Face Observed Limits.

IF 5.1 2区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Foods Pub Date : 2025-02-27 DOI:10.3390/foods14050822
Federica Della Cerra, Mariapia Esposito, Simonetta Caira, Andrea Scaloni, Francesco Addeo
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Abstract

This study critically examines the limitations of the official Italian methodology used for detecting bovine adulteration milk in Protected Designation of Origin (PDO) Mozzarella di Bufala Campana (MdBC). This method focuses on the whey fraction of cheese samples, which comprises about 1% of total MdBC proteins, and is based on a high-performance liquid chromatography (HPLC) quantification of the bovine β-lactoglobulin A (β-Lg A) as a marker. Here, we have demonstrated that this official methodology suffers from measurement inconsistencies due to its reliance on raw bovine whey standards, which fail to account for β-Lg genetic polymorphisms in real MdBC samples and protein thermal modifications during cheesemaking. To overcome these limitations, we propose a dual proteomics-based approach using matrix-assisted laser desorption ionization (MALDI-TOF) mass spectrometry (MS) and nano-HPLC-electrospray (ESI)-tandem mass spectrometry (MS/MS) analysis of MdBC extracted whey. MALDI-TOF-MS focused on identifying proteotypic peptides specific to bovine and buffalo β-Lg and α-lactalbumin (α-La), enabling high specificity for distinguishing the two animal species at adulteration levels as low as 1%. Complementing this, nano-HPLC-ESI-MS/MS provided a comprehensive profile by identifying over 100 bovine-specific peptide markers from β-Lg, α-La, albumin, lactoferrin, and osteopontin. Both methods ensured precise detection and quantification of bovine milk adulteration in complex matrices like pasta filata cheeses, achieving high sensitivity even at minimal adulteration levels. Accordingly, the proposed dual proteomics-based approach overcomes challenges associated with whey protein polymorphism, heat treatment, and processing variability, and complements casein-based methodologies already validated under European standards. This integrated framework of analyses focused on whey and casein fraction enhances the reliability of adulteration detection and safeguards the authenticity of PDO buffalo mozzarella, upholding its unique quality and integrity.

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使用意大利官方方法检测受保护原产地水牛马苏里拉奶酪中牛乳清蛋白的挑战:一种蛋白质组学方法来面对观察到的限制。
本研究批判性地考察了意大利官方用于检测原产地指定保护(PDO)马苏里拉迪Bufala坎帕纳(MdBC)中牛掺假牛奶的方法的局限性。该方法以牛β-乳球蛋白a (β-Lg a)的高效液相色谱(HPLC)定量为标记物,重点分析奶酪样品的乳清部分,其中乳清部分约占MdBC总蛋白的1%。在这里,我们已经证明,由于依赖于生牛乳清标准,这种官方方法存在测量不一致的问题,这无法解释真实MdBC样品中的β-Lg遗传多态性和奶酪制作过程中的蛋白质热修饰。为了克服这些限制,我们提出了一种基于蛋白质组学的双方法,使用基质辅助激光解吸电离(MALDI-TOF)质谱(MS)和纳米高效液相色谱-电喷雾(ESI)-级联质谱(MS/MS)分析MdBC提取乳清。MALDI-TOF-MS专注于鉴定牛和水牛特有的蛋白型肽β-Lg和α-乳清蛋白(α-La),在掺假水平低至1%的情况下具有高特异性区分这两种动物物种。作为补充,纳米hplc - esi -MS/MS通过鉴定超过100种牛特异性肽标记提供了全面的资料,包括β-Lg、α-La、白蛋白、乳铁蛋白和骨桥蛋白。这两种方法都确保了对复杂基质中掺假的牛乳的精确检测和定量,即使在最低掺假水平下也能实现高灵敏度。因此,提出的基于双蛋白质组学的方法克服了与乳清蛋白多态性、热处理和加工变异性相关的挑战,并补充了已经在欧洲标准下验证的基于酪蛋白的方法。这种针对乳清和酪蛋白部分的综合分析框架提高了掺假检测的可靠性,保障了PDO水牛马苏里拉奶酪的真实性,维护了其独特的质量和完整性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Foods
Foods Immunology and Microbiology-Microbiology
CiteScore
7.40
自引率
15.40%
发文量
3516
审稿时长
15.83 days
期刊介绍: Foods (ISSN 2304-8158) is an international, peer-reviewed scientific open access journal which provides an advanced forum for studies related to all aspects of food research. It publishes reviews, regular research papers and short communications. Our aim is to encourage scientists, researchers, and other food professionals to publish their experimental and theoretical results in as much detail as possible or share their knowledge with as much readers unlimitedly as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, unique features of this journal: Ÿ manuscripts regarding research proposals and research ideas will be particularly welcomed Ÿ electronic files or software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material Ÿ we also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds
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