Anna Maria Gioacchini

Dr. Anna Maria Gioacchini

University of Urbino "Carlo Bo"

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

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

Representative Publications

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16 September 2008 in Rapid Communications in Mass Spectrometry
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AGAnna Maria Gioacchini
Anna Maria Gioacchini
MMMichele Menotta
Michele Menotta
Michele GuesciniMichele Guescini
Michele Guescini
RSRoberta Saltarelli
Roberta Saltarelli
PCPaola Ceccaroli
Paola Ceccaroli
VSVilberto Stocchi
Vilberto Stocchi


5 November 2010 in Rapid Communications in Mass Spectrometry
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AGAnna Maria Gioacchini
Anna Maria Gioacchini
MSMauro De Santi
Mauro De Santi
Michele GuesciniMichele Guescini
Michele Guescini
GBGiorgio Brandi
Giorgio Brandi
VSVilberto Stocchi
Vilberto Stocchi

3 August 2018 in Fungal Biology
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AAAntonella Amicucci
Antonella Amicucci
Elena BarbieriElena Barbieri
Elena Barbieri
VSValentina Sparvoli
Valentina Sparvoli
AGAnna Maria Gioacchini
Anna Maria Gioacchini
CCCinzia Calcabrini
Cinzia Calcabrini
Alessandra ZambonelliAlessandra Zambonelli
Alessandra Zambonelli
Tuber magnatum Pico, the delectable white truffle, is one of the most expensive foods on the market today, and thanks to its delicious aroma, flavour and unique organoleptic properties, it is considered the most prized truffle species in the world. In this study, we examined the reddish pigmentation that frequently occurs in T. magnatum ascomata for the presence of pigment-producing bacteria. Despite the colour variation, this alteration does not seem to affect the characteristic aroma of the ascoma. The aim of this study was to detect and molecularly identify the bacterial communities within the reddish-pigmented regions of T. magnatum ascomata. The inner part of the reddish-pigmented region of three T. magnatum ascomata collected in North-Central Italy was analysed. This reddish part was used to establish a bacterial culture collection and to extract the total genomic DNA in order to obtain a library of 16S rDNAs representative of the bacterial community. The molecular approach revealed limited microbial diversity within the reddish-pigmented regions compared to the wider range of bacterial species commonly found at the same maturation stage and season in T. magnatum ascomata. The pigmented regions showed a prevalence of specific bacterial species belonging to α-, β- and γ- Proteobacteria, Actinobacteria and Firmicutes. From the tandem mass spectrometry analysis of the extracted pigment, four compounds were identified: i) bixin, ii) β-carotene, iii) cis-1-glycosyl-apo-8'- lycopene and iv) the fucoxanthin. Carotenoid producing species such as Microbacterium and Chryseobacterium emerged as the most likely cause of the peculiar reddish pigment production. Indeed, our findings suggest that the peculiar reddish pigment might be produced by these bacterial species.

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PAPatrizia Ambrogini
Patrizia Ambrogini
DLDavide Lattanzi
Davide Lattanzi
MPMichael Di Palma
Michael Di Palma
Caterina CiacciCaterina Ciacci
Caterina Ciacci
DSDavid Savelli
David Savelli
RCRiccardo Cuppini
Riccardo Cuppini
Experimental evidence highlights the involvement of the endoplasmic reticulum (ER)-mediated Ca2+ signals in modulating synaptic plasticity and spatial memory formation in the hippocampus. Ca2+ release from the ER mainly occurs through two classes of Ca2+ channels, inositol 1,4,5-trisphosphate receptors (InsP3Rs) and ryanodine receptors (RyRs). Calsequestrin (CASQ) and calreticulin (CR) are the most abundant Ca2+-binding proteins allowing ER Ca2+ storage. The hippocampus is one of the brain regions expressing CASQ, but its role in neuronal activity, plasticity, and the learning processes is poorly investigated. Here, we used knockout mice lacking both CASQ type-1 and type-2 isoforms (double (d)CASQ-null mice) to: a) evaluate in adulthood the neuronal electrophysiological properties and synaptic plasticity in the hippocampal Cornu Ammonis 1 (CA1) field and b) study the performance of knockout mice in spatial learning tasks. The ablation of CASQ increased the CA1 neuron excitability and improved the long-term potentiation (LTP) maintenance. Consistently, (d)CASQ-null mice performed significantly better than controls in the Morris Water Maze task, needing a shorter time to develop a spatial preference for the goal. The Ca2+ handling analysis in CA1 pyramidal cells showed a decrement of Ca2+ transient amplitude in (d)CASQ-null mouse neurons, which is consistent with a decrease in afterhyperpolarization improving LTP. Altogether, our findings suggest that CASQ deletion affects activity-dependent ER Ca2+ release, thus facilitating synaptic plasticity and spatial learning in post-natal development.