Books > Professional & Technical > Biochemical engineering
|
Buy Now
Using Mass Spectrometry for Biochemical Studies on Enzymatic Domains from Polyketide Synthases (Paperback, Softcover reprint of the original 1st ed. 2016)
Loot Price: R3,299
Discovery Miles 32 990
|
|
Using Mass Spectrometry for Biochemical Studies on Enzymatic Domains from Polyketide Synthases (Paperback, Softcover reprint of the original 1st ed. 2016)
Series: Springer Theses
Expected to ship within 10 - 15 working days
|
This thesis reports studies on the substrate specificity of crucial
ketosynthase (KS) domains from trans-AT Polyketide Synthases
(PKSs). Using a combination of electrospray ionisation-mass
spectrometry (ESI-MS) and simple N-acetyl cysteamine (SNAC)
substrate mimics, the specificity of a range of KS domains from the
bacillaene and psymberin PKSs have been succsessfully studied with
regard to the initial acylation step of KS-catalysis. In addition,
the ability to alter the substrate tolerance of KS domains by
simple point mutations in the active site has been demonstrated. A
series of acyl-ACPs have been synthesised using a novel methodology
and employed to probe the substrate specificity of both KS domains
and the previously uncharcterised acyl hydrolase domain, PedC.
KS-catalysed chain elongation reactions have also been conducted
and monitored by ESI-MS/MS. All KS domains studied exhibited higher
substrate specificity at the elongation step than in the preceeding
acylation step. Furthermore, a mechanism of reversible acylation is
proposed using the PsyA ACP1-KS1 di-domain. The findings in this
thesis provide important insights into mechanisms of KS specificity
and show that mutagenesis can be used to expand the repertoire of
acceptable substrates for future PKS engineering.
General
Is the information for this product incomplete, wrong or inappropriate?
Let us know about it.
Does this product have an incorrect or missing image?
Send us a new image.
Is this product missing categories?
Add more categories.
Review This Product
No reviews yet - be the first to create one!
|
You might also like..
|
Email address subscribed successfully.
A activation email has been sent to you.
Please click the link in that email to activate your subscription.