Al-Zuhair, S and Ashraf, S and Hisaindee, S and Darmaki, NA and Battah, S and Svistunenko, D and Reeder, BJ and Stanway, G and Chaudhary, A (2017) Enzymatic pre-treatment of microalgae cells for enhanced extraction of proteins. Engineering in Life Sciences, 17 (2). pp. 175-185. DOI https://doi.org/10.1002/elsc.201600127
Al-Zuhair, S and Ashraf, S and Hisaindee, S and Darmaki, NA and Battah, S and Svistunenko, D and Reeder, BJ and Stanway, G and Chaudhary, A (2017) Enzymatic pre-treatment of microalgae cells for enhanced extraction of proteins. Engineering in Life Sciences, 17 (2). pp. 175-185. DOI https://doi.org/10.1002/elsc.201600127
Al-Zuhair, S and Ashraf, S and Hisaindee, S and Darmaki, NA and Battah, S and Svistunenko, D and Reeder, BJ and Stanway, G and Chaudhary, A (2017) Enzymatic pre-treatment of microalgae cells for enhanced extraction of proteins. Engineering in Life Sciences, 17 (2). pp. 175-185. DOI https://doi.org/10.1002/elsc.201600127
Abstract
<jats:p>Crude proteins and pigments were extracted from different microalgae strains, both marine and freshwater. The effectiveness of enzymatic pre‐treatment prior to protein extraction was evaluated and compared to conventional techniques, including ultrasonication and high‐pressure water extraction. Enzymatic pre‐treatment was chosen as it could be carried out at mild shear conditions and does not subject the proteins to high temperatures, as with the ultrasonication approach. Using enzymatic pre‐treatment, the extracted proteins yields of all tested microalgae strains were approximately 0.7 mg per mg of dry cell weight. These values were comparable to those achieved using a commercial lytic kit. Ultrasonication was not very effective for proteins extraction from <jats:italic>Chlorella sp</jats:italic>., and the extracted proteins yields did not exceed 0.4 mg per mg of dry cell weight. For other strains, similar yields were achieved by both treatment methods. The time‐course effect of enzymatic incubation on the proteins extraction efficiency was more evident using laccase compared to lysozyme, which suggested that the former enzyme has a slower rate of cell disruption. The crude extracted proteins were fractionated using an ion exchange resin and were analyzed by the electrophoresis technique. They were further tested for their antioxidant activity, the highest of which was about 60% from <jats:italic>Nannochloropsis sp</jats:italic>. The total phenolic contents in the selected strains were also determined, with <jats:italic>Chlorella sp</jats:italic>. showing the highest content reaching 17 mg/g. Lysozyme was also found to enhance the extraction of pigments, with <jats:italic>Chlorella</jats:italic> sp. showing the highest pigments contents of 16.02, 4.59 and 5.22 mg/g of chlorophyll a, chlorophyll b and total carotenoids, respectively.</jats:p>
Item Type: | Article |
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Uncontrolled Keywords: | Cell disruption; Enzymes; Microalgae; Pigments; Proteins |
Subjects: | Q Science > QH Natural history > QH301 Biology |
Divisions: | Faculty of Science and Health Faculty of Science and Health > Life Sciences, School of |
SWORD Depositor: | Unnamed user with email elements@essex.ac.uk |
Depositing User: | Unnamed user with email elements@essex.ac.uk |
Date Deposited: | 09 Sep 2016 09:40 |
Last Modified: | 07 Aug 2024 18:31 |
URI: | http://repository.essex.ac.uk/id/eprint/17566 |
Available files
Filename: Al-Zuhair_et_al-2016-Engineering_in_Life_Sciences.pdf