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Using Mass Spectrometry for Biochemical Studies on Enzymatic Domains from Polyketide Synthases (Paperback, Softcover reprint of the original 1st ed. 2016) Loot Price: R3,471
Discovery Miles 34 710
Using Mass Spectrometry for Biochemical Studies on Enzymatic Domains from Polyketide Synthases (Paperback, Softcover reprint of...

Using Mass Spectrometry for Biochemical Studies on Enzymatic Domains from Polyketide Synthases (Paperback, Softcover reprint of the original 1st ed. 2016)

Matthew Jenner

Series: Springer Theses

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Loot Price R3,471 Discovery Miles 34 710 | Repayment Terms: R325 pm x 12*

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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

Imprint: Springer International Publishing AG
Country of origin: Switzerland
Series: Springer Theses
Release date: May 2018
First published: 2016
Authors: Matthew Jenner
Dimensions: 235 x 155 x 11mm (L x W x T)
Format: Paperback
Pages: 176
Edition: Softcover reprint of the original 1st ed. 2016
ISBN-13: 978-3-319-81355-4
Categories: Books > Medicine > Pre-clinical medicine: basic sciences > General
Books > Professional & Technical > Biochemical engineering > General
Books > Science & Mathematics > Biology, life sciences > Biochemistry > General
Books > Professional & Technical > Industrial chemistry & manufacturing technologies > Industrial chemistry > Chemical engineering
Books > Science & Mathematics > Chemistry > Analytical chemistry > Qualitative analytical chemistry > Chemical spectroscopy, spectrochemistry > General
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LSN: 3-319-81355-2
Barcode: 9783319813554

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