Alexander Dikiy

Prof. Alexander Dikiy


Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

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

Representative Publications

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1 October 2015 in Food Chemistry
Verified
Journal Article
Open access
ESElena Shumilina
Elena Shumilina
ACAlessandra Ciampa
Alessandra Ciampa
Francesco CapozziFrancesco Capozzi
Francesco Capozzi
TRTurid Rustad
Turid Rustad
ADAlexander Dikiy
Alexander Dikiy
High resolution NMR technique has been used to monitor post-mortem changes in salmon (Salmo salar) fillets upon storage at 4 and 0°C. Thirty-one different fish metabolites influencing freshness and taste properties have been unequivocally assigned by NMR using either available standard compounds or ad hoc acquired 2D (1)H-(1)H TOCSY and (1)H-(13)С HSQC spectra. The monitored fish metabolites include amino acids, dipeptides, sugars, vitamins, biogenic amines, as well as different products of the ATP degradation. The detection and monitoring of biogenic amines by NMR, upon fish storage, is information of interest for consumers, since some of these compounds are toxic. The data from this study shows that NMR spectroscopy also provides the amount of all metabolites necessary for the calculation of the K-index used to express fish freshness. A good correlation was found between the K-index increase and the formation of the undesired biogenic amines. The metabolite concentrations and the K-index found in this work were compared and found coherent with literature data. The performed study reveals the strengths and the suitability of the NMR approach to monitor different biochemical processes occurring during fish storage and qualitatively and quantitatively characterise fish metabolites determining fish quality.

1 October 2010 in Journal of Biological Chemistry
Verified
Journal Article
Open access
FAFinn Aachmann
Finn Aachmann
LSLena S. Sal
Lena S. Sal
HKHwa-Young Kim
Hwa-Young Kim
SMStefano M. Marino
Stefano M. Marino
VGVadim N. Gladyshev
Vadim N. Gladyshev
ADAlexander Dikiy
Alexander Dikiy
Methionine sulfoxide reductases protect cells by repairing oxidatively damaged methionine residues in proteins. Here, we report the first three-dimensional structure of the mammalian selenoprotein methionine sulfoxide reductase B1 (MsrB1), determined by high resolution NMR spectroscopy. Heteronuclear multidimensional spectra yielded NMR spectral assignments for the reduced form of MsrB1 in which catalytic selenocysteine (Sec) was replaced with cysteine (Cys). MsrB1 consists of a central structured core of two β-sheets and a highly flexible, disordered N-terminal region. Analysis of pH dependence of NMR signals of catalytically relevant residues, comparison with the data for bacterial MsrBs, and NMR-based structural analysis of methionine sulfoxide (substrate) and methionine sulfone (inhibitor) binding to MsrB1 at the atomic level reveal a mechanism involving catalytic Sec(95) and resolving Cys(4) residues in catalysis. The MsrB1 structure differs from the structures of Cys-containing MsrBs in the use of distal selenenylsulfide, residues needed for catalysis, and the mode in which the active form of the enzyme is regenerated. In addition, this is the first structure of a eukaryotic zinc-containing MsrB, which highlights the structural role of this metal ion bound to four conserved Cys. We integrated this information into a structural model of evolution of MsrB superfamily.

7 February 2011 in Journal of Proteome Research
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Journal Article
Closed access
Francesco MusianiFrancesco Musiani
Francesco Musiani
Stefano CiurliStefano Ciurli
Stefano Ciurli
ADAlexander Dikiy
Alexander Dikiy

24 November 2013 in JBIC Journal of Biological Inorganic Chemistry
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Journal Article
Open access
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ESElena Shumilina
Elena Shumilina
ODOlena Dobrovolska
Olena Dobrovolska
RCRebecca Del Conte
Rebecca Del Conte
HHHenrik Waldal Holen
Henrik Waldal Holen
ADAlexander Dikiy
Alexander Dikiy
Expression of the mammalian enzyme methionine sulfoxide reductase B1 (MsrB1) in Escherichia coli growing in cobalt-containing media resulted in the reproducible appearance of the stable cobalt-containing protein MsrB1-Co. NMR studies and biocomputing using the programs AnisoFit and Amber allowed us to generate a structure of MsrB1-Co sharing the overall fold with the native zinc-containing protein MsrB1-Zn. Our data suggest that the N-terminus containing resolving cysteine tends to be closer to the protein’s catalytic center than was previously reported. It is argued that this proximity supports the proposed catalytic mechanism and ensures high catalytic efficiency of MsrB1. Functional studies showed that both MsrB1-Zn and MsrB1-Co exhibit similar levels of activity, in agreement with the structural studies performed. The proposed metal ion substitution approach may have a methodological significance in determining whether methionine sulfoxide reductase B proteins contain a metal ion.

2 August 2011 in Proteins: Structure, Function, and Bioinformatics
Verified
Journal Article
Closed access
PDF file
FAFinn Aachmann
Finn Aachmann
GKGeun‐Hee Kwak
Geun‐Hee Kwak
RCRebecca Del Conte
Rebecca Del Conte
HKHwa‐Young Kim
Hwa‐Young Kim
VGVadim N. Gladyshev
Vadim N. Gladyshev
ADAlexander Dikiy
Alexander Dikiy

29 November 2019 in Foods
Verified
Journal Article
Open access
PDF file
Even KirkholtEven Kirkholt
Even Kirkholt
ADAlexander Dikiy
Alexander Dikiy
ESElena Shumilina
Elena Shumilina
This study shows the potential of improving the taste and shelf life of salmon by storing it in conjunction with sugar kelp. The influence of the addition of wet sugar kelp to Atlantic salmon fillet was assessed using a Nuclear Magnetic Resonance (NMR) metabolomics approach. Seaweed treatment caused significant changes in the polar and non-polar metabolic composition of salmon muscle upon its storage. The mutual diffusion of sugar kelp and salmon metabolites caused a significant decrease of the formation of the off-smelling compound trimethylamine and the biogenic amines, along with an increase of umami-related compounds (aspartate and succinic acid). Carotenoid composition of the seaweed-treated samples significantly differs from the reference samples. The amount of wet seaweeds used for the treatment and the time passed after the fish slaughter influence salmon quality parameters.