Niel van Wyk

Dr. Niel van Wyk

Department of Molecular Sciences, Faculty of Science and Engineering, Sydney, NSW 2109, Australia
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Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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26 February 2015 in Molecular Microbiology
Verified
Journal Article
Open access
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SFS. Fishbein
S. Fishbein
NWNiel van Wyk
Niel van Wyk
RWR. M. Warren
R. M. Warren
SSSamantha Sampson
Samantha Sampson
Summary: The pe/ppe genes represent one of the most intriguing aspects of the Mycobacterium tuberculosis genome. These genes are especially abundant in pathogenic mycobacteria, with more than 160 members in M. tuberculosis. Despite being discovered over 15 years ago, their function remains unclear, although various lines of evidence implicate selected family members in mycobacterial virulence. In this review, we use PE/PPE phylogeny as a framework within which we examine the diversity and putative functions of these proteins. We report on the evolution and diversity of the respective gene families, as well as the implications thereof for function and host immune recognition. We summarize recent findings on pe/ppe gene regulation, also placing this in the context of PE/PPE phylogeny. We collate data from several large proteomics datasets, providing an overview of PE/PPE localization, and discuss the implications this may have for host responses. Assessment of the current knowledge of PE/PPE diversity suggests that these proteins are not variable antigens as has been so widely speculated; however, they do clearly play important roles in virulence. Viewing the growing body of pe/ppe literature through the lens of phylogeny reveals trends in features and function that may be associated with the evolution of mycobacterial pathogenicity.

14 November 2019 in Journal of Agricultural and Food Chemistry
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Journal Article
Closed access
NWNiel van Wyk
Niel van Wyk
MGManfred Grossmann
Manfred Grossmann
JWJürgen Wendland
Jürgen Wendland
CWChristian von Wallbrunn
Christian von Wallbrunn
IPIsak Pretorius
Isak Pretorius

29 November 2013 in Biotechnology for Biofuels
Verified
Journal Article
Open access
PDF file
IMIsa Jacoba Marx
Isa Jacoba Marx
NWNiel van Wyk
Niel van Wyk
SSSalome Smit
Salome Smit
DJDaniel Jacobson
Daniel Jacobson
MVMarinda Viljoen-Bloom
Marinda Viljoen-Bloom
HVHeinrich Volschenk
Heinrich Volschenk
Background: The lignocellulosic enzymes of Trichoderma species have received particular attention with regard to biomass conversion to biofuels, but the production cost of these enzymes remains a significant hurdle for their commercial application. In this study, we quantitatively compared the lignocellulolytic enzyme profile of a newly isolated Trichoderma asperellum S4F8 strain with that of Trichoderma reesei Rut C30, cultured on sugarcane bagasse (SCB) using solid-state fermentation (SSF). Results: Comparison of the lignocellulolytic enzyme profiles of S4F8 and Rut C30 showed that S4F8 had significantly higher hemicellulase and β-glucosidase enzyme activities. Liquid chromatography tandem mass spectrometry analysis of the two fungal secretomes enabled the detection of 815 proteins in total, with 418 and 397 proteins being specific for S4F8 and Rut C30, respectively, and 174 proteins being common to both strains. In-depth analysis of the associated biological functions and the representation of glycoside hydrolase family members within the two secretomes indicated that the S4F8 secretome contained a higher diversity of main and side chain hemicellulases and β-glucosidases, and an increased abundance of some of these proteins compared with the Rut C30 secretome. Conclusions: In SCB SSF, T. asperellum S4F8 produced a more complex lignocellulolytic cocktail, with enhanced hemicellulose and cellobiose hydrolysis potential, compared with T. reesei Rut C30. This bodes well for the development of a more cost-effective and efficient lignocellulolytic enzyme cocktail from T. asperellum for lignocellulosic feedstock hydrolysis.

23 February 2023 in Critical Reviews in Biotechnology
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Journal Article
Open access
NWNiel van Wyk
Niel van Wyk
JBJennifer Badura
Jennifer Badura
CWChristian von Wallbrunn
Christian von Wallbrunn
IPIsak Pretorius
Isak Pretorius
As a metaphor, lemons get a bad rap; however the proverb ‘if life gives you lemons, make lemonade’ is often used in a motivational context. The same could be said of Hanseniaspora in winemaking. Despite its predominance in vineyards and grape must, this lemon-shaped yeast is underappreciated in terms of its contribution to the overall sensory profile of fine wine. Species belonging to this apiculate yeast are known for being common isolates not just on grape berries, but on many other fruits. They play a critical role in the early stages of a fermentation and can influence the quality of the final product. Their deliberate addition within mixed-culture fermentations shows promise in adding to the complexity of a wine and thus provide sensorial benefits. Hanseniaspora species are also key participants in the fermentations of a variety of other foodstuffs ranging from chocolate to apple cider. Outside of their role in fermentation, Hanseniaspora species have attractive biotechnological possibilities as revealed through studies on biocontrol potential, use as a whole-cell biocatalyst and important interactions with Drosophila flies. The growing amount of ‘omics data on Hanseniaspora is revealing interesting features of the genus that sets it apart from the other Ascomycetes. This review collates the fields of research conducted on this apiculate yeast genus.

1 February 2013 in Applied Energy
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Journal Article
Closed access
HKHeinrich Kroukamp
Heinrich Kroukamp
RDRiaan DenHaan
Riaan DenHaan
NWNiel van Wyk
Niel van Wyk
WZWillem Heber van Zyl
Willem Heber van Zyl

1 December 2019 in Trends in Genetics
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Journal Article
Closed access
IBIgnacio Belda
Ignacio Belda
JRJavier Ruiz
Javier Ruiz
ASAntonio Santos
Antonio Santos
NWNiel van Wyk
Niel van Wyk
IPIsak Pretorius
Isak Pretorius