Please use this identifier to cite or link to this item:
|Title:||Cloning and characterization of a novel lipase from Vibrio harveyi strain AP6|
p -Nitrophenyl esters
|Source:||Teo, J.W.P., Zhang, L.-H., Poh, C.L. (2003-07-17). Cloning and characterization of a novel lipase from Vibrio harveyi strain AP6. Gene 312 (1-2) : 181-188. ScholarBank@NUS Repository. https://doi.org/10.1016/S0378-1119(03)00615-2|
|Abstract:||A lipolytic enzyme designated Vst, was cloned from Vibrio harveyi strain AP6. The vst gene was 1650 bp and was predicted to encode a 549 amino acid precursor with a molecular mass of about 61 kDa. The predicted polypeptide shared about 30% sequence identity with Bacillus esterases. Sequence alignment of Vst and related esterases revealed the presence of an active site serine located in the middle of the GESAG motif, at positions 212-216. This motif resembled the GXSXG consensus motif characteristic of lipolytic enzymes. Vst was expressed as a carboxy-terminal 6×His tagged recombinant enzyme from E. coli TOP10 cells. SDS-PAGE and Western blot analysis using anti-His antibodies confirmed that the size of the mature protein was about 61 kDa. Substrate specificity of Vst was investigated using p -nitrophenyl (p NP) esters with varying carbon chain lengths, from C2 to C18. Vst showed the highest activity with the long chain p -nitrophenyl ester p NPC12 but was able to hydrolyze longer chain esters (p NPC 14-p NPC16) as well as short and medium chain esters (p NPC4 and p NPC8). © 2003 Elsevier Science B.V. All rights reserved.|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Feb 21, 2018
WEB OF SCIENCETM
checked on Jan 16, 2018
checked on Feb 18, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.