Natasha Hungerford

Dr. Natasha Hungerford

Queensland Alliance for Agriculture and Food Innovation (QAAFI), The University of Queensland, Health and Food Sciences Precinct, Coopers Plains, QLD 4108, Australia
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Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

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

Representative Publications

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22 July 2020 in Scientific Reports
Verified
Journal Article
Open access
PDF file
Mary T. FletcherMary T. Fletcher
Mary T. Fletcher
NHNatasha Hungerford
Natasha Hungerford
DWDennis Webber
Dennis Webber
MJMatheus Carpinelli de Jesus
Matheus Carpinelli de Jesus
JZJiali Zhang
Jiali Zhang
Norhasnida ZawawiNorhasnida Zawawi
Norhasnida Zawawi
Stingless bee (Meliponini) honey has long been considered a high-value functional food, but the perceived therapeutic value has lacked attribution to specific bioactive components. Examination of honey from five different stingless bee species across Neotropical and Indo-Australian regions has enabled for the first time the identification of the unusual disaccharide trehalulose as a major component representing between 13 and 44 g per 100 g of each of these honeys. Trehalulose is an isomer of sucrose with an unusual α-(1 → 1) glucose-fructose glycosidic linkage and known acariogenic and low glycemic index properties. NMR and UPLC-MS/MS analysis unambiguously confirmed the identity of trehalulose isolated from stingless bee honeys sourced across three continents, from Tetragonula carbonaria and Tetragonula hockingsi species in Australia, from Geniotrigona thoracica and Heterotrigona itama in Malaysia and from Tetragonisca angustula in Brazil. The previously unrecognised abundance of trehalulose in stingless bee honeys is concrete evidence that supports some of the reported health attributes of this product. This is the first identification of trehalulose as a major component within a food commodity. This study allows the exploration of the expanded use of stingless bee honey in foods and identifies a bioactive marker for authentication of this honey in associated food standards.

20 October 2020 in Toxins
Verified
Journal Article
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ZLZhi Hung Loh
Zhi Hung Loh
DODiane Ouwerkerk
Diane Ouwerkerk
AKAthol V. Klieve
Athol V. Klieve
NHNatasha Hungerford
Natasha Hungerford
Mary T. FletcherMary T. Fletcher
Mary T. Fletcher
Animal feeds may contain exogenous compounds that can induce toxicity when ruminants ingest them. These toxins are secondary metabolites originating from various sources including plants, bacteria, algae and fungi. Animal feed toxins are responsible for various animal poisonings which negatively impact the livestock industry. Poisoning is more frequently reported in newly exposed, naïve ruminants while ‘experienced’ ruminants are observed to better tolerate toxin-contaminated feed. Ruminants can possess detoxification ability through rumen microorganisms with the rumen microbiome able to adapt to utilise toxic secondary metabolites. The ability of rumen microorganisms to metabolise these toxins has been used as a basis for the development of preventative probiotics to confer resistance against the poisoning to naïve ruminants. In this review, detoxification of various toxins, which include plant toxins, cyanobacteria toxins and plant-associated fungal mycotoxins, by rumen microorganisms is discussed. The review will include clinical studies of the animal poisoning caused by these toxins, the toxin mechanism of action, toxin degradation by rumen microorganisms, reported and hypothesised detoxification mechanisms and identified toxin metabolites with their toxicity compared to their parent toxin. This review highlights the commercial potential of rumen inoculum derived probiotics as viable means of improving ruminant health and production.

1 March 1999 in Tetrahedron Letters
Verified
Journal Article
Closed access
TCTimothy D.W. Claridge
Timothy D.W. Claridge
DLDaniel D. Long
Daniel D. Long
NHNatasha Hungerford
Natasha Hungerford
RARobin T. Aplin
Robin T. Aplin
MSMartin D. Smith
Martin D. Smith
GFGeorge W.J. Fleet
George W.J. Fleet

14 February 2006 in Organic Letters
Verified
Journal Article
Closed access
ILIgnace Louis
Ignace Louis
NHNatasha Hungerford
Natasha Hungerford
EHEdward J. Humphries
Edward J. Humphries
MMMalcolm D. McLeod
Malcolm D. McLeod

19 October 2000 in Journal of the Chemical Society, Perkin Transactions 1
Verified
Journal Article
Closed access
PDF file
NHNatasha Hungerford
Natasha Hungerford
TCTimothy D. W. Claridge
Timothy D. W. Claridge
MWMark P. Watterson
Mark P. Watterson
RARobin T. Aplin
Robin T. Aplin
ANDRES MORENOANDRES MORENO
ANDRES MORENO
GFGeorge W. J. Fleet
George W. J. Fleet
The synthesis of a D-allo-5-(azidomethyl)tetrahydrofuran-2-carboxylate as an amino acid precursor (in which the carboxylic acid is cis to the azidomethyl substituent and trans to the diol moiety) is reported from D-ribose. The oligomerisation of this monomer to dimeric, tetrameric and octameric carbopeptoids is described. NMR studies into the solution structures of cyclohexylidene-protected oligomers and of a deprotected tetramer with eight free hydroxy groups are described.

1 March 1999 in Tetrahedron Letters
Verified
Journal Article
Closed access
DLDaniel D. Long
Daniel D. Long
NHNatasha Hungerford
Natasha Hungerford
MSMartin D. Smith
Martin D. Smith
DBDominic E.A. Brittain
Dominic E.A. Brittain
DMDaniel G. Marquess
Daniel G. Marquess
GFGeorge W.J. Fleet
George W.J. Fleet