Allergenic risk assessment of porcine myoglobin expressed by engineered Komagataella Phaffii

IF 6.2 3区 综合性期刊 Q1 Multidisciplinary Fundamental Research Pub Date : 2024-09-01 DOI:10.1016/j.fmre.2023.11.017
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Abstract

Myoglobin produced by fermentation using engineered Komagataella phaffii is an important color additive in meat analogue products, but its allergenicity is poorly understood. Here, we initially searched the Allergen Online database and did not find any allergic or cross-reactive proteins in porcine myoglobin (PM). In vitro simulated digestion demonstrated that PM did not exhibit notable acid-base resistance or anti-digestion capabilities. However, sensitization was observed in BALB/c mice, including a significant increase in specific antibodies and biomarkers for allergic reactions, as well as alterations in gut microbiome and serum metabolome. Interestingly, the intensity of sensitization exhibited a negative correlation with the purity of PM. 60% and 88% purities showed weaker sensitization compared to the ovalbumin control group. These allergic reactions were likely due to the non-myoglobin protein portion, highlighting the importance of purification processes and the urgent need to assess the allergenicity of this portion.

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猪肌红蛋白的过敏风险评估
通过使用工程化的 Komagataella phaffii 发酵产生的肌红蛋白是肉类类似产品中的一种重要色素添加剂,但对其过敏性却知之甚少。在此,我们初步搜索了过敏原在线数据库,没有在猪肌红蛋白(PM)中发现任何过敏或交叉反应蛋白。体外模拟消化表明,猪肌红蛋白没有表现出明显的耐酸碱性或抗消化能力。然而,在 BALB/c 小鼠体内观察到了致敏现象,包括特异性抗体和过敏反应生物标志物的显著增加,以及肠道微生物组和血清代谢组的改变。有趣的是,过敏的强度与 PM 的纯度呈负相关。与卵清蛋白对照组相比,纯度为60%和88%的可吸入颗粒物的致敏程度较弱。这些过敏反应很可能是由非肌红蛋白部分引起的,这凸显了纯化过程的重要性以及评估这部分蛋白质过敏性的迫切需要。
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来源期刊
Fundamental Research
Fundamental Research Multidisciplinary-Multidisciplinary
CiteScore
4.00
自引率
1.60%
发文量
294
审稿时长
79 days
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