429 results match your criteria: "Biomolecular Interaction Centre[Affiliation]"
Genome Announc
March 2018
The Biodesign Center for Fundamental and Applied Microbiomics, Center for Evolution and Medicine, School of Life Sciences, Arizona State University, Tempe, Arizona, USA
is a ubiquitous and parasitic mite of honey bees, infecting them with pathogenic viruses having a major impact on apiculture. We identified two novel circular replication-associated protein (Rep)-encoding single-stranded (CRESS) DNA viruses from sampled from a honey bee hive near Christchurch in New Zealand.
View Article and Find Full Text PDFAntibiotics (Basel)
February 2018
Biomolecular Interaction Centre and School of Biological Sciences, University of Canterbury, Christchurch 8041, New Zealand.
There is growing concern about the emergence of bacterial strains showing resistance to all classes of antibiotics commonly used in human medicine. Despite the broad range of available antibiotics, bacterial resistance has been identified for every antimicrobial drug developed to date. Alarmingly, there is also an increasing prevalence of multidrug-resistant bacterial strains, rendering some patients effectively untreatable.
View Article and Find Full Text PDFFront Microbiol
February 2018
Plant Protection Research Division, Agroscope, Zurich, Switzerland.
In light of public concerns over the use of pesticides and antibiotics in plant protection and the subsequent selection for spread of resistant bacteria in the environment, it is inevitable to broaden our knowledge about viable alternatives, such as natural antagonists and their mode of action. The genus is known for its metabolic versatility and genetic plasticity, encompassing pathogens as well as antagonists. We characterized strain F9, an isolate from apple flowers in a Swiss orchard, and determined its antagonistic activity against several phytopathogenic bacteria, in particular , the causal agent of fire blight.
View Article and Find Full Text PDFBiochem Biophys Res Commun
March 2018
School of Biological Sciences, University of Auckland, Auckland 1010, New Zealand; MacDiarmid Institute for Advanced Materials and Nanotechnology, Victoria University, Wellington 6140, New Zealand; School of Chemical Sciences, University of Auckland, Auckland 1010, New Zealand. Electronic address:
Peroxiredoxins are abundant peroxidase enzymes that are key regulators of the cellular redox environment. A major subgroup of these proteins, the typical 2-Cys peroxiredoxins, can switch between dimers and decameric or dodecameric rings, during the catalytic cycle. The necessity of this change in quaternary structure for function as a peroxidase is not fully understood.
View Article and Find Full Text PDFBeilstein J Org Chem
January 2018
Department of Chemistry, University of Canterbury, Private Bag 4800, Christchurch, 8140, New Zealand.
Glycoscience, despite its myriad of challenges, promises to unravel the causes of, potential new detection methods for, and novel therapeutic strategies against, many disease states. In the last two decades, glyco-gold nanoparticles have emerged as one of several potential new tools for glycoscientists. Glyco-gold nanoparticles consist of the unique structural combination of a gold nanoparticle core and an outer-shell comprising multivalent presentation of carbohydrates.
View Article and Find Full Text PDFCarbohydr Res
March 2018
Department of Chemistry, University of Canterbury, Private Bag 4800, Christchurch, 8140, New Zealand; Biomolecular Interaction Centre, University of Canterbury, Private Bag 4800, Christchurch, 8140, New Zealand. Electronic address:
The recently discovered enzyme Mycobacterium tuberculosis thymidine monophosphate kinase (TMPKmt), which catalyses the phosphorylation of deoxythymidine monophosphate (dTMP) to give deoxythymidine diphosphate (dTDP), is indispensable for the growth and survival of M. tuberculosis as it plays an essential role in DNA synthesis. Inhibition of TMPKmt is an attractive avenue for the development of novel anti-tuberculosis agents.
View Article and Find Full Text PDFGenome Announc
January 2018
Ferrier Research Institute, Victoria University of Wellington, Wellington, New Zealand
strain MF5954 (ATCC 74245) (formerly classified as sp.) is a filamentous fungal species known for its production of the secondary metabolite nodulisporic acid A. We present here the 41.
View Article and Find Full Text PDFJ Am Chem Soc
January 2018
Ferrier Research Institute, Victoria University of Wellington, Wellington 6012, New Zealand.
Nodulisporic acids comprise a group of valuable indole diterpenes that exhibit potent insecticidal activities. We report the identification of a gene cluster in the genome of the filamentous fungus Hypoxylon pulicicidum (Nodulisporium sp.) that contains genes responsible for the biosynthesis of nodulisporic acids.
View Article and Find Full Text PDFBiophys Rev
April 2018
Biomolecular Interaction Centre and School of Biological Sciences, University of Canterbury, P.O. Box 4800, Christchurch, 8140, New Zealand.
Eukaryotic cell surfaces are decorated with a complex array of glycoconjugates that are usually capped with sialic acids, a large family of over 50 structurally distinct nine-carbon amino sugars, the most common member of which is N-acetylneuraminic acid. Once made available through the action of neuraminidases, bacterial pathogens and commensals utilise host-derived sialic acid by degrading it for energy or repurposing the sialic acid onto their own cell surface to camouflage the bacterium from the immune system. A functional sialic acid transporter has been shown to be essential for the uptake of sialic acid in a range of human bacterial pathogens and important for host colonisation and persistence.
View Article and Find Full Text PDFJ Chromatogr A
January 2018
School of Product Design, University of Canterbury, New Zealand; Institute for Bioengineering, School of Engineering, The University of Edinburgh, Edinburgh EH9 3FB, UK.
Ordered packing has previously been considered for porous media applications in the industrial and analytical worlds, with implementation constrained only by the lack of feasible fabrication methods. Additive manufacturing now provides the answer to this limitation, which leads to the novel domain of customized ordered packing and a variety of optimized geometries. In this work, the chromatographic behaviour of ordered configurations of particles was described using computational fluid dynamics methods based on the Lattice Boltzmann Model.
View Article and Find Full Text PDFBiochem J
January 2018
Maurice Wilkins Centre, Biomolecular Interaction Centre and Department of Chemistry, University of Canterbury, Christchurch 8041, New Zealand
Biochem J
January 2018
Biomolecular Interaction Centre and School of Biological Sciences, University of Canterbury, Christchurch, New Zealand
Dihydrodipicolinate reductase (DHDPR) catalyses the second reaction in the diaminopimelate pathway of lysine biosynthesis in bacteria and plants. In contrast with the tetrameric bacterial DHDPR enzymes, we show that DHDPR from (grape) and are dimeric in solution. In the present study, we have also determined the crystal structures of DHDPR enzymes from the plants and , which are the first dimeric DHDPR structures.
View Article and Find Full Text PDFData Brief
December 2017
Maurice Wilkins Centre for Molecular Biodiscovery and School of Biological Sciences, University of Auckland, 3 Symonds Street, Auckland 1142, New Zealand.
There are twenty-five published structures anthranilate phosphoribosyltransferase (-AnPRT) that use the same crystallization protocol. The structures include protein complexed with natural and alternative substrates, protein:inhibitor complexes, and variants with mutations of substrate-binding residues. Amongst these are varying space groups (2, 2, 222, 222).
View Article and Find Full Text PDFMol Biol Evol
January 2018
Department of Biology and Biochemistry, University of Houston, Houston, TX.
The fitness effects of mutations can depend on the genetic backgrounds in which they occur and thereby influence future opportunities for evolving populations. In particular, mutations that fix in a population might change the selective benefit of subsequent mutations, giving rise to historical contingency. We examine these effects by focusing on mutations in a key metabolic gene, pykF, that arose independently early in the history of 12 Escherichia coli populations during a long-term evolution experiment.
View Article and Find Full Text PDFISME J
January 2018
CIRAD, UMR BGPI, Montpellier, France.
Disease emergence events regularly result from human activities such as agriculture, which frequently brings large populations of genetically uniform hosts into contact with potential pathogens. Although viruses cause nearly 50% of emerging plant diseases, there is little systematic information about virus distribution across agro-ecological interfaces and large gaps in understanding of virus diversity in nature. Here we applied a novel landscape-scale geometagenomics approach to examine relationships between agricultural land use and distributions of plant-associated viruses in two Mediterranean-climate biodiversity hotspots (Western Cape region of South Africa and Rhône river delta region of France).
View Article and Find Full Text PDFLab Chip
October 2017
Biomolecular Interaction Centre, Department of Electrical and Computer Engineering, University of Canterbury, New Zealand.
Oomycetes and fungi are microorganisms whose pathogenic (invasive) growth can cause diseases that are responsible for significant ecological and economic losses. Such growth requires the generation of a protrusive force, the magnitude and direction of which involves a balance between turgor pressure and localised yielding of the cell wall and the cytoskeleton. To study invasive growth in individual hyphae we have developed a lab-on-a-chip platform with integrated force-sensors based on elastomeric polydimethylsiloxane (PDMS) micro-pillars.
View Article and Find Full Text PDFACS Chem Biol
October 2017
Maurice Wilkins Centre, Biomolecular Interaction Centre and Department of Chemistry, University of Canterbury, P.O. Box 4800, Christchurch 8140, New Zealand.
Adenosine triphosphate phosphoribosyltransferase (ATP-PRT) catalyzes the first step in histidine biosynthesis, a pathway essential to microorganisms and a validated target for antimicrobial drug design. The ATP-PRT enzyme catalyzes the reversible substitution reaction between phosphoribosyl pyrophosphate and ATP. The enzyme exists in two structurally distinct forms, a short- and a long-form enzyme.
View Article and Find Full Text PDFBiochim Biophys Acta Proteins Proteom
February 2018
Maurice Wilkins Centre for Molecular Biodiscovery and School of Biological Sciences, University of Auckland, 3A Symonds Street, Auckland 1142, New Zealand; School of Biological Sciences, University of Auckland, 3 Symonds Street, Auckland 1142, New Zealand. Electronic address:
Phosphoribosyltransferases (PRTs) bind 5'-phospho-α-d-ribosyl-1'-pyrophosphate (PRPP) and transfer its phosphoribosyl group (PRib) to specific nucleophiles. Anthranilate PRT (AnPRT) is a promiscuous PRT that can phosphoribosylate both anthranilate and alternative substrates, and is the only example of a type III PRT. Comparison of the PRPP binding mode in type I, II and III PRTs indicates that AnPRT does not bind PRPP, or nearby metals, in the same conformation as other PRTs.
View Article and Find Full Text PDFExpert Rev Proteomics
October 2017
a Food & Bio-Based Products, AgResearch Ltd ., Lincoln , New Zealand.
In several biomedical research fields, the cross-linking of peptides and proteins has an important impact on health and wellbeing. It is therefore of crucial importance to study this class of post-translational modifications in detail. The huge potential of mass spectrometric technologies in the mapping of these protein-protein cross-links is however overshadowed by the challenges that the field has to overcome.
View Article and Find Full Text PDFJ Appl Microbiol
October 2017
Microbiology of Plant Foods, Agroscope, Waedenswil, Switzerland.
Aim: Investigate dynamics of culturable mesophilic bacteria and selected food-contaminating bacteria from three herbs and their production environment.
Methods And Results: Marjoram, basil and thyme were investigated during one growing season by sampling plants, organic fertilizers, soil, irrigation water and marketed products. Mesophilic bacteria and selected food-contaminating bacteria (Escherichia coli, Enterococcus spp.
Chem Commun (Camb)
July 2017
School of Biological Sciences, The University of Auckland, 3A Symonds Street, Auckland 1010, New Zealand and Maurice Wilkins Centre for Molecular Biodiscovery, The University of Auckland, 3 Symonds St, Auckland, New Zealand and School of Chemical Sciences, The University of Auckland, 23 Symonds Street, Auckland 1010, New Zealand.
Advanced lipid peroxidation end-products (ALEs) accumulate with ageing and oxidative stress-related diseases. Despite their potential therapeutic value, there are no suitably protected ALE building blocks reported in the literature to enable their site-specific incorporation into synthetic peptides. The synthesis of an Fmoc-protected ALE building block, N-(3-methylpyridinium)lysine (MP-lysine) and its incorporation into collagen model peptides is reported.
View Article and Find Full Text PDFPLoS One
October 2017
Maurice Wilkins Centre for Molecular Biodiscovery, Biomolecular Interaction Centre and Department of Chemistry, University of Canterbury, Christchurch, New Zealand.
EMBO Rep
August 2017
Institute of Biochemistry II, Goethe University School of Medicine, Frankfurt (Main), Germany
Through the canonical LC3 interaction motif (LIR), [W/F/Y]-X-X-[I/L/V], protein complexes are recruited to autophagosomes to perform their functions as either autophagy adaptors or receptors. How these adaptors/receptors selectively interact with either LC3 or GABARAP families remains unclear. Herein, we determine the range of selectivity of 30 known core LIR motifs towards individual LC3s and GABARAPs.
View Article and Find Full Text PDFBiochem Biophys Res Commun
July 2017
Biomolecular Frontiers Research Centre and Department of Chemistry and Biomolecular Sciences, Macquarie University, New South Wales 2109, Australia. Electronic address:
We have exploited the self-assembling properties of archaeal-derived protein Lsmα to generate new supramolecular forms based on its stable ring-shaped heptamer. We show that engineered ring tectons incorporating cysteine sidechains on obverse faces of the Lsmα toroid are capable of forming paired and stacked formations. A Cys-modified construct, N10C/E61C-Lsmα, appears to organize into disulfide-mediated tube formations up to 45 nm in length.
View Article and Find Full Text PDFChem Sci
March 2017
Department of Chemistry , University of Canterbury, Private Bag 4800 , Christchurch , 8140 , New Zealand . Email:
High yielding selective acetylation of only the anomeric hydroxyl of unprotected sugars is possible in aqueous solution using 2-chloro-1,3-dimethylimidazolinium chloride (DMC), thioacetic acid, and a suitable base. The reaction, which may be performed on a multi-gram scale, is stereoselective for sugars that possess a hydroxyl group at position-2, exclusively yielding the 1,2- products. The use of an iterative reagent addition procedure allows the use of sodium carbonate as the base, avoiding the formation of triethylammonium salts, which may hamper product purification.
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