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Extraction of phycocyanin—A natural blue colorant from dried spirulina biomass: Influence of processing parameters and extraction techniques

机译:从干燥螺旋藻生物质中提取天然植物色素藻蓝蛋白:工艺参数和提取技术的影响

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摘要

Phycocyanin, a natural blue colorant, is typically extracted from liquid biomass of Arthrospira platensis, a blue-green algae called spirulina. In this study, we developed a scalable process to extract phycocyanin from dried spirulina biomass. First, we established the optimal ionic strength and pH for the extraction buffer. The results showed that a minimum ionic strength (>5 g/L NaCl) must be maintained to minimize the co-extraction of the green chlorophyll. The optimal pH of the phosphate buffer (100 mM) for phycocyanin extraction is 7.5; however, the pH should be immediately adjusted to 6.0 to 6.5 after the extraction to keep phycocyanin stable. Second, we also investigated three processing techniques, that is, high-pressure processing (HPP), pulsed electric field (PEF), and ultrasonication, to break the cell walls of spirulina and facilitate the release of phycocyanins into extraction buffers. HPP and PEF do not lead to the release of phycocyanin into the extraction buffer. However, ultrasonication breaks down the spirulina into fine particles and releases most of the phycocyanin, along with other impurities, immediately after the treatment. Last, it has been revealed that most of the phycocyanin can be extracted from biomass within 3 hr by phosphate buffer only (pH 7.5, 100 mM) at room temperature. It is concluded that there is no need to treat the rehydrated biomass solution by HPP, PEF, or ultrasonication due to the minimal benefits they brought for the extraction. Based on these results, we proposed an extraction process for the plant production of phycocyanin starting from dried spirulina biomass.
机译:藻蓝蛋白是一种天然的蓝色着色剂,通常从Arthrospira platensis(一种称为螺旋藻的蓝绿藻)的液体生物质中提取。在这项研究中,我们开发了从干螺旋藻生物质中提取藻蓝蛋白的可扩展方法。首先,我们确定了提取缓冲液的最佳离子强度和pH。结果表明,必须保持最低离子强度(> 5 g / L NaCl),以最大程度地减少绿色叶绿素的共萃取。用于藻蓝蛋白提取的磷酸盐缓冲液的最佳pH(100 mM)为7.5;但是,提取后应立即将pH值调节至6.0至6.5,以保持藻蓝蛋白稳定。其次,我们还研究了三种处理技术,即高压处理(HPP),脉冲电场(PEF)和超声处理,以破坏螺旋藻的细胞壁并促进藻蓝蛋白释放到提取缓冲液中。 HPP和PEF不会导致藻蓝蛋白释放到提取缓冲液中。然而,超声处理后立即将螺旋藻分解成细颗粒,并释放出大部分藻蓝蛋白以及其他杂质。最后,已经揭示了大多数藻蓝蛋白可以在室温下仅用磷酸盐缓冲液(pH 7.5,100 mM)在3小时内从生物质中提取。结论是,由于HPP,PEF或超声波处理对提取物带来的收益极小,因此无需通过HPP,PEF或超声处理处理过的生物质溶液。基于这些结果,我们提出了一种从干燥的螺旋藻生物质中提取植物藻蓝蛋白的提取方法。

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