TY - JOUR
T1 - Integration Process for Protein Extraction from Microalgae Using Liquid Biphasic Electric Flotation (LBEF) System
AU - Sankaran, Revathy
AU - Show, Pau Loke
AU - Cheng, Yu Shen
AU - Tao, Yang
AU - Ao, Xia
AU - Nguyen, Thi Dong Phuong
AU - Van Quyen, Dong
N1 - Funding Information:
This study is supported by the Fundamental Research Grant Scheme (Malaysia, FRGS/1/2015/SG05/UNIM/03/1), the Ministry of Science and Technology, and (MOSTI 02-02-12-SF0256), the Prototype Research Grant Scheme (PRGS/2/2015/SG05/UNIM/03/1). In addition, the authors would like to appreciate and offer their special thanks to Chew Sho Yin, Bong Jiang Chier, Lau Shyan Zhin, and Tang Chin Yi for providing the initial supports to this study.
Publisher Copyright:
© 2018, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2018/10/1
Y1 - 2018/10/1
N2 - Microalgae are the most promising sources of protein, which have high potential due to their high-value protein content. Conventional methods of protein harnessing required multiple steps, and they are generally complex, time consuming, and expensive. Currently, the study of integration methods for microalgae cell disruption and protein recovery process as a single-step process is attracting considerable interest. This study aims to investigate the novel approach of integration method of electrolysis and liquid biphasic flotation for protein extraction from wet biomass of Chlorella sorokiniana CY-1 and obtaining the optimal operating conditions for the protein extraction. The optimized conditions were found at 60% (v/v) of 1-propanol as top phase, 250 g/L of dipotassium hydrogen phosphate as bottom phase, crude microalgae loading of 0.1 g, air flowrate of 150 cc/min, flotation time of 10 min, voltage of 20 V and electrode’s tip touching the top phase of LBEF. The protein recovery and separation efficiency after optimization were 23.4106 ± 1.2514% and 173.0870 ± 4.4752%, respectively. Comparison for LBEF with and without the aid of electric supply was also conducted, and it was found that with the aid of electrolysis, the protein recovery and separation efficiency increased compared to the LBEF without electrolysis. This novel approach minimizes the steps for overall protein recovery from microalgae, time consumption, and cost of operation, which is beneficial in bioprocessing industry.
AB - Microalgae are the most promising sources of protein, which have high potential due to their high-value protein content. Conventional methods of protein harnessing required multiple steps, and they are generally complex, time consuming, and expensive. Currently, the study of integration methods for microalgae cell disruption and protein recovery process as a single-step process is attracting considerable interest. This study aims to investigate the novel approach of integration method of electrolysis and liquid biphasic flotation for protein extraction from wet biomass of Chlorella sorokiniana CY-1 and obtaining the optimal operating conditions for the protein extraction. The optimized conditions were found at 60% (v/v) of 1-propanol as top phase, 250 g/L of dipotassium hydrogen phosphate as bottom phase, crude microalgae loading of 0.1 g, air flowrate of 150 cc/min, flotation time of 10 min, voltage of 20 V and electrode’s tip touching the top phase of LBEF. The protein recovery and separation efficiency after optimization were 23.4106 ± 1.2514% and 173.0870 ± 4.4752%, respectively. Comparison for LBEF with and without the aid of electric supply was also conducted, and it was found that with the aid of electrolysis, the protein recovery and separation efficiency increased compared to the LBEF without electrolysis. This novel approach minimizes the steps for overall protein recovery from microalgae, time consumption, and cost of operation, which is beneficial in bioprocessing industry.
KW - Electric
KW - Integration
KW - Liquid biphasic flotation
KW - Microalgae
KW - Protein
UR - http://www.scopus.com/inward/record.url?scp=85052127316&partnerID=8YFLogxK
U2 - 10.1007/s12033-018-0111-6
DO - 10.1007/s12033-018-0111-6
M3 - Article
C2 - 30116991
AN - SCOPUS:85052127316
SN - 1073-6085
VL - 60
SP - 749
EP - 761
JO - Molecular Biotechnology
JF - Molecular Biotechnology
IS - 10
ER -