Nature inspired engineering: bioprospecting for novel psychrophilic enzymes from the Antarctic tunicate, Salpa thompsoni

Nature-inspired engineering offers an alternative approach to solving key sustainability challenges in bioprocessing by looking to fundamental mechanisms that occur in nature for inspiration on solutions to key bioprocessing obstacles. The degradation of cellulosic materials at low temperatures pose...

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Bibliographic Details
Main Author: Cotton, Alexander Ross
Format: Doctoral or Postdoctoral Thesis
Language:English
Published: UCL (University College London) 2022
Subjects:
Online Access:https://discovery.ucl.ac.uk/id/eprint/10144350/2/Full%20Thesis_Final_Accepted_20220228.pdf
https://discovery.ucl.ac.uk/id/eprint/10144350/
Description
Summary:Nature-inspired engineering offers an alternative approach to solving key sustainability challenges in bioprocessing by looking to fundamental mechanisms that occur in nature for inspiration on solutions to key bioprocessing obstacles. The degradation of cellulosic materials at low temperatures poses an interesting challenge of how to degrade a recalcitrant starting material in a context that is thermodynamically challenging. A case study of a set of marine invertebrates known as salps was explored for two key reasons: their ability to rapidly filter feed upon microalgae and their gelatinous composition formed of tunicin, a variety of cellulose. Taking this as a departure point, this research targeted a unique pelagic organism surviving in the cold waters surrounding Antarctica, Salpa thompsoni, from which novel psychrophilic carbohydrate active enzymes (CAZymes) were identified using a bioprospecting approach. A transcriptomic dataset was prepared from S. thompsoni which was interrogated alongside a publicly available draft genome. This resulted in the identification of several novel hydrolytic enzymes. Two of the identified cellulases, a putative β-glucosidase (BglS) and putative endoglucanase (EgS), were recombinantly expressed and assayed. BglS was found to display β-glucosidase-like activity when hydrolysing pNPG as a substrate, with a Topt of 20°C. To the authors knowledge, this is the lowest observed Topt of any previously described β-glucosidase. EgS displayed low levels of endoglucanase-like activity when hydrolysing CMC as a substrate however, further characterisation of this putative endoglucanase was inhibited due to low expression levels. Initial characterisation of BglS and EgS provided some evidence for their ability to hydrolyse cellulosic materials. As such, these results indicate potential future use of these enzymes in cellulosic biomass pretreatment. In addition, bioprospecting for novel biocatalysts was carried out in the field on a British Antarctic Survey (BAS) research cruise. Salpa ...