Sara Obeid, Hussein Rida, Jérôme Peydecastaing, Hosni Takache, Ali Ismail, Pierre-Yves Pontalier
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引用次数: 0
摘要
采用超声辅助提取和膜过滤的方法对蓝藻螺旋藻进行分离,得到纯藻蓝蛋白部分和澄清后不含叶绿素和类胡萝卜素的无色蛋白部分。评估压力和功率对总蛋白释放的影响。然后通过超滤,有和没有硫酸铵沉淀来评估提取蛋白质的保留率。在低频率(12 kHz)、常压、超声功率为200瓦(W)的条件下,水溶液中总蛋白的回收率达到97%。采用硫酸铵(25% W /v)沉淀法去除粗蛋白提取物中的色素和杂质。最后,半正面超滤导致保留液中c -藻蓝蛋白的高回收率:10和100 kda切断膜分别为95%和91%。然而,在100 kda切断膜的情况下,渗透室中总非色素蛋白的水平不超过67%。本文提出了一种分离螺旋藻两种不同蛋白质组分的方法。
Coupling ultrasound and membrane filtration for the fractionation of Spirulina platensis sp. and the recovery of phycocyanin and pigment-free proteins.
The cyanobacterium Spirulina platensis was subjected to a fractionation process involving ultrasound-assisted extraction and membrane filtration to obtain a pure phycocyanin fraction and a clarified colorless protein fraction free of chlorophyll and carotenoids. The effects of pressure and power on total protein release were assessed. The retention of the extracted proteins was then assessed by ultrafiltration, with and without ammonium sulfate precipitation. Total protein recovery yields reached 97% in aqueous solution, at a low frequency (12 kHz), atmospheric pressure, and with an ultrasonic power of 200 Watts (W). Ammonium sulfate (25% w/v) precipitation was used to remove pigments and impurities from the crude protein extract. Finally, semi-frontal ultrafiltration resulted in high levels of C-phycocyanin recovery in the retentate: 95% and 91% with 10 and 100 kDa-cutoff membranes, respectively. However, the levels of total non-pigmented proteins in the permeate compartment did not exceed 67% with a 100 kDa-cutoff membrane. A fractionation process is proposed here for the valorization of two different protein fractions from Spirulina platensis.
期刊介绍:
Biotechnology Letters is the world’s leading rapid-publication primary journal dedicated to biotechnology as a whole – that is to topics relating to actual or potential applications of biological reactions affected by microbial, plant or animal cells and biocatalysts derived from them.
All relevant aspects of molecular biology, genetics and cell biochemistry, of process and reactor design, of pre- and post-treatment steps, and of manufacturing or service operations are therefore included.
Contributions from industrial and academic laboratories are equally welcome. We also welcome contributions covering biotechnological aspects of regenerative medicine and biomaterials and also cancer biotechnology. Criteria for the acceptance of papers relate to our aim of publishing useful and informative results that will be of value to other workers in related fields.
The emphasis is very much on novelty and immediacy in order to justify rapid publication of authors’ results. It should be noted, however, that we do not normally publish papers (but this is not absolute) that deal with unidentified consortia of microorganisms (e.g. as in activated sludge) as these results may not be easily reproducible in other laboratories.
Papers describing the isolation and identification of microorganisms are not regarded as appropriate but such information can be appended as supporting information to a paper. Papers dealing with simple process development are usually considered to lack sufficient novelty or interest to warrant publication.