Partitioning behavior of recombinant lipase in Escherichia coli by ionic liquid-based aqueous two-phase systems. Issue 86 (31st August 2016)
- Record Type:
- Journal Article
- Title:
- Partitioning behavior of recombinant lipase in Escherichia coli by ionic liquid-based aqueous two-phase systems. Issue 86 (31st August 2016)
- Main Title:
- Partitioning behavior of recombinant lipase in Escherichia coli by ionic liquid-based aqueous two-phase systems
- Authors:
- Hadzir, Muhammad Hakimi
Abbasiliasi, Sahar
Ariff, Arbakariya B.
Yusoff, Siti Baidurah
Ng, Hui Suan
Tan, Joo Shun - Abstract:
- Abstract : Evaluations of ILATPSs were performed with a variety of ionic liquids and salts as phase components to figure out their competencies in the recovery of lipase from a fermentation broth of E. coli using banana waste as a substrate. Abstract : There has been significant interest in ionic liquid aqueous two-phase systems (ILATPSs) with properties such as rapid phase segregation which can lead to a reduction in time taken for protein recovery. Evaluations of ILATPSs were performed with various types of ionic liquid ((Emim)BF4, (Emim)Br, (Bmim)BF4, and (Bmim)Br) and salts (potassium-, sodium-, and magnesium-based) as phase components to figure out their competencies in the recovery of lipase from a fermentation broth of E. coli using banana waste as a substrate. The results of this study revealed that an ILATPS comprising (Emim)Br/potassium phosphate significantly enhanced lipase recovery upon partitioning lipase. Optimization of the composition of the ILATPS using response surface methodology (RSM) significantly improved the purification factor ( P F ) and partition coefficient ( K e ). The influences of crude loading ( C L ), pH changes, and the presence of NaCl on the recovery performance were also studied. Recovery of E. coli BL21 lipase was accomplished in an (Emim)Br/potassium phosphate ILATPS using 26.5% (w/w) (Emim)Br, 19% (w/w) potassium phosphate at pH 7.6, 3% NaCl and a crude loading of 7% (w/w). Using this ILATPS, lipase was successfully recovered in aAbstract : Evaluations of ILATPSs were performed with a variety of ionic liquids and salts as phase components to figure out their competencies in the recovery of lipase from a fermentation broth of E. coli using banana waste as a substrate. Abstract : There has been significant interest in ionic liquid aqueous two-phase systems (ILATPSs) with properties such as rapid phase segregation which can lead to a reduction in time taken for protein recovery. Evaluations of ILATPSs were performed with various types of ionic liquid ((Emim)BF4, (Emim)Br, (Bmim)BF4, and (Bmim)Br) and salts (potassium-, sodium-, and magnesium-based) as phase components to figure out their competencies in the recovery of lipase from a fermentation broth of E. coli using banana waste as a substrate. The results of this study revealed that an ILATPS comprising (Emim)Br/potassium phosphate significantly enhanced lipase recovery upon partitioning lipase. Optimization of the composition of the ILATPS using response surface methodology (RSM) significantly improved the purification factor ( P F ) and partition coefficient ( K e ). The influences of crude loading ( C L ), pH changes, and the presence of NaCl on the recovery performance were also studied. Recovery of E. coli BL21 lipase was accomplished in an (Emim)Br/potassium phosphate ILATPS using 26.5% (w/w) (Emim)Br, 19% (w/w) potassium phosphate at pH 7.6, 3% NaCl and a crude loading of 7% (w/w). Using this ILATPS, lipase was successfully recovered in a single purification step, which gave a yield, P F and K e of 93.75%, 3.394 and 1.352, respectively. A high P F value indicates that (Emim)Br/potassium phosphate is capable of attaining an excellent degree of lipase purity, suggesting that the proposed ILATPS is suitable for implementation in a large scale process for lipase purification. … (more)
- Is Part Of:
- RSC advances. Volume 6:Issue 86(2016)
- Journal:
- RSC advances
- Issue:
- Volume 6:Issue 86(2016)
- Issue Display:
- Volume 6, Issue 86 (2016)
- Year:
- 2016
- Volume:
- 6
- Issue:
- 86
- Issue Sort Value:
- 2016-0006-0086-0000
- Page Start:
- 82571
- Page End:
- 82580
- Publication Date:
- 2016-08-31
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6ra16722e ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 7.xml