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dc.contributor.advisorZhang, Hu-
dc.contributor.advisorJin, Bo-
dc.contributor.authorMisson, Mailin-
dc.date.issued2016-
dc.identifier.urihttp://hdl.handle.net/2440/103557-
dc.description.abstractEnzyme immobilization has been recognized as a promising technique to enhance enzyme stability, activity and reusability for the development of cost-effective, green and sustainable biotechnological processes. Recent development in nanotechnology has opened a new frontier for diverse nano-scale enzyme carriers. The immobilization of enzyme onto nanomaterials produces a nanobiocatalyst assembly, which maximizes reaction efficiencies by favoring desirable chemical reaction kinetics and selectivity for substrates, while the unique properties of nanocarriers offer a revolution of biocatalyst applications in the bioprocessing field. Nevertheless, the issues of enzyme leakage and conformational changes make the translation of the biocatalyst technology into commercial practices technically challenging and economically infeasible. Hence, investigating new technologies for fabricating the nanobiocatalyst with promising biocatalytic activities and functionalities is of great importance. In this PhD research, nanoparticle- and nanofiber-based enzyme carriers were developed and explored to immobilize β-galactosidase for conversion of lactose from dairy industry wastes into galacto-oligosaccharide (GOS) as a high value product. The structure-function relationship for the nanocarrier, the enzyme-nanocarrier microenvironment and the enzyme-nanocarrier nanobiocatalyst structure were extensively evaluated, aiming to enhance the bioengineering performance of the nanobiocatalysts. Dendrimer-like silica nanoparticles (HPSNs) with hierarchical pores were synthesized, characterized and functionalized with amino (NH2) and carboxyl group (COOH) to facilitate enzyme binding. Our findings revealed that surface functionalization can promote enzyme affinity towards the nanomaterial interface and selectively enhance enzyme reusability and its catalytic activity for improving the GOS production yield. A systematic synthesis of polystyrene nanofibers (PSNFs) was executed by optimizing key fabrication parameters using the electrospinning technique, including polymer concentration, electric voltage and distance between discharge needle tips and the collector. Surface modification of the PSNF was found to improve enzyme loading and activity. In addition, the local microenvironment of the nanobiocatalysts was able to optimize the enzyme selectivity and specificity, resulting in favouring transgalactosylation over hydrolysis for the lactose bioconversion. Further investigation to enhance the enzyme stability and catalytic activity at various operating conditions was conducted. PSNFs were chosen as the enzyme carrier owing to their scaling up potential in a manufacturing reactor system with their excellent mechanical and structural properties. Immobilizing β-galactosidase on the modified PSNF surface facilitated formation of stable enzyme binding and exhibited distinguished catalytic performance. Thermal and pH stability were improved significantly while the recyclability was enhanced from four to nine cycles. The evaluation of lactose conversion performance showed an improved GOS yield from 14 to 28% in comparison to free β-galactosidase. To advance the knowledge of understanding β-galactosidase binding on the PSNF surface, the β-galactosidase/nanofiber nanobiocatalyst structure were comprehensively analyzed. Characterizations on the nanobiocatalyst properties were performed before and after biocatalyst immobilization. The analysis using scanning electron microscope (SEM), fluorescence microscope, Fourier transform infrared spectroscopy (FTIR), and Raman spectroscopy demonstrated successful biocatalyst attachment, homogenous distributions and no conformation changes. The effectiveness factor for lactose conversion into galacto-oligosaccharides (GOS) in a disc-stacked column reactor indicated distinguished biocatalyst performance in comparison to the free counterpart. Finally, a scalable recirculating spiral reactor was designed in-house and operated for a continuous GOS production using the nanofibers-β-galactosidase nanobiocatalyst. The PSNF-β-galactosidase performed better in GOS production yield by exceeding the free counterpart about 1.5 to 3.7-fold. The variable parameters of the bioreactor system such as reaction time, feed flow rate and initial substrate concentration were found to have a profound effect in optimizing GOS synthesis. The best GOS production yield was determined at 159 g/l with 86% lactose conversion under the optimal operating conditions of 24 h reaction time, 15 ml/min flow rate and 400 g/l initial lactose concentration. Overall, nanoparticles- and nanofibers-immobilized β-galactosidase nanobiocatalysts were successfully developed and assessed for conversion of lactose into GOS in this study. The nanobiocatalyst assembly demonstrated remarkable selectivity towards transgalactosylation to produce GOS from lactose.Comparing with free enzyme, the immobilized β-galactosidase significantly enhanced enzymatic activities, leading to excellent bioconversion performance. The distinguished bioengineering perfomance of nanofiber-immobilized β-galactosidase in a scalable recirculating spiral bioreactor indicates their great potential for a large scale and continuous process application. Furthermore, the understanding of the binding mechanism for the enzyme and its nanoscale support surface and the nanobiocatalyst structure can be a key driver for fabricating biocatalyst-nanomaterial hybrids and improving biocatalyst efficiency. In summary, the findings of this study provide new insights into the development of economically and industrially viable nanobiocatalysts for industry-scale bioprocesses.en
dc.subjectnandbiocatalystsen
dc.subjectimmobilizationen
dc.subjectβ-galactosidaseen
dc.subjectnanofibersen
dc.subjectnanoparticlesen
dc.subjectbioprocessen
dc.titlePreparation and characterization of β-galactosidase nanobiocatalysts and its application for galacto-oligosaccharides productionen
dc.typeThesesen
dc.contributor.schoolSchool of Chemical Engineeringen
dc.provenanceCopyright material removed from digital thesis. See print copy in University of Adelaide Library for full text.en
dc.provenanceThis electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exceptions. If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals-
dc.description.dissertationThesis (Ph.D.) (Research by Publication) -- University of Adelaide, School of Chemical Engineering, 2016.en
dc.identifier.doi10.4225/55/58b667940d33e-
Appears in Collections:Research Theses

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