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从绿叶中提取蛋白质:利用的关键步骤概述。

Recovery of protein from green leaves: Overview of crucial steps for utilisation.

作者信息

Tamayo Tenorio Angelica, Gieteling Jarno, de Jong Govardus A H, Boom Remko M, van der Goot Atze J

机构信息

Laboratory of Food Process Engineering, Wageningen University, PO Box 17, 6700 AA Wageningen, The Netherlands.

Netherlands Organisation for Applied Scientific Research - TNO, PO Box 360, 3704 HE Zeist, The Netherlands.

出版信息

Food Chem. 2016 Jul 15;203:402-408. doi: 10.1016/j.foodchem.2016.02.092. Epub 2016 Feb 15.

Abstract

Plant leaves are a major potential source of novel food proteins. Till now, leaf protein extraction methods mainly focus on the extraction of soluble proteins, like rubisco protein, leaving more than half of all protein unextracted. Here, we report on the total protein extraction from sugar beet leaves (Beta vulgaris L.) by a traditional thermal extraction method consisting of mechanical pressing, heating to 50 °C and centrifugation. The resulting streams (i.e. supernatant, green-protein pellet and fibrous pulp) were characterised in terms of composition, physical structure and processing options. The protein distributed almost equally over the supernatant, pellet and pulp. This shows that thermal precipitation is an unselective process with respect to fractionation between soluble (rubisco) and insoluble (other) proteins. About 6% of the total protein could be extracted as pure rubisco (90% purity) from the supernatant. Surfactants commonly used for protein solubilisation could hardly re-dissolve the precipitated proteins in the pellet phase, which suggested that irreversible association was induced between the co-precipitated proteins and cell debris. Thus, the extraction of this protein will require prevention of their co-precipitation, and should take place in the original juice solution.

摘要

植物叶片是新型食品蛋白质的一个主要潜在来源。到目前为止,叶蛋白提取方法主要集中于可溶性蛋白的提取,如核酮糖-1,5-二磷酸羧化酶蛋白,导致超过一半的蛋白质未被提取。在此,我们报道了通过一种传统热提取方法从甜菜叶(Beta vulgaris L.)中提取总蛋白,该方法包括机械压榨、加热至50°C和离心。对所得物流(即上清液、绿色蛋白沉淀和纤维状果肉)的组成、物理结构和加工选项进行了表征。蛋白质几乎均匀地分布在上清液、沉淀和果肉中。这表明热沉淀对于可溶性(核酮糖-1,5-二磷酸羧化酶)和不溶性(其他)蛋白质之间的分级分离是一个非选择性过程。约6%的总蛋白可以从上清液中作为纯核酮糖-1,5-二磷酸羧化酶(纯度90%)提取出来。常用于蛋白质增溶的表面活性剂几乎无法使沉淀在沉淀相中的蛋白质重新溶解,这表明共沉淀蛋白质与细胞碎片之间诱导了不可逆缔合。因此,这种蛋白质的提取需要防止其共沉淀,并且应该在原汁溶液中进行。

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