2020
DOI: 10.1021/acs.jafc.0c04251
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Efficient Imaging of Saccharomyces cerevisiae Based on B- and N-Doped Carbon Dots

Abstract: The estimation of yeast viability with B- and N-doped carbon dots (BN-CDs) was investigated in this paper. BN-CDs with a fluorescent quantum yield of 65.47% were prepared by a one-step hydrothermal method. The size distribution of BN-CDs was relatively narrow, with the majority falling within 7.5–8.5 nm, and they were mainly composed of carbon, oxygen, nitrogen, and boron. BN-CDs were shown to have strong and stable fluorescence. They exhibited excitation-independent photoluminescence property, which could avo… Show more

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Cited by 21 publications
(9 citation statements)
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“…Thakur et al first combined ciprofloxacin with CDs to form a Cipro@C-dots conjugate, which could perform in vivo imaging of Saccharomyces cerevisiae (yeast) and emit bright green fluorescence. 71 Similar imaging of CDs in living fungi was also observed in Valsa Mali Miyabe et Yamada, 87 Aspergillus aculeatus, 88,89 Saccharomyces cerevisiae, 90 Colletotrichum gloeosporioides, 91 and Fusarium oxysporum. 92 When CDs were prepared with bacteria as a precursor, the imaging application of CDs can be observed in dead fungal cells Saccharomyces cerevisiae (yeast) and Trichoderma reesei.…”
Section: The Mechanism Of Cds Against Fungisupporting
confidence: 63%
“…Thakur et al first combined ciprofloxacin with CDs to form a Cipro@C-dots conjugate, which could perform in vivo imaging of Saccharomyces cerevisiae (yeast) and emit bright green fluorescence. 71 Similar imaging of CDs in living fungi was also observed in Valsa Mali Miyabe et Yamada, 87 Aspergillus aculeatus, 88,89 Saccharomyces cerevisiae, 90 Colletotrichum gloeosporioides, 91 and Fusarium oxysporum. 92 When CDs were prepared with bacteria as a precursor, the imaging application of CDs can be observed in dead fungal cells Saccharomyces cerevisiae (yeast) and Trichoderma reesei.…”
Section: The Mechanism Of Cds Against Fungisupporting
confidence: 63%
“…Figure 2b shows the absorption peak at 3456 cm −1 corresponding to the N–H or O–H stretching vibrations. The peak at 2875 cm −1 was ascribed to the C–H stretching vibrations, while the sharp peak at 1788 cm −1 was observed due to the C=O stretching vibrations in the carboxyl group [36]. The peak at 1645 cm −1 was assigned to the characteristic amide bond (O=C–NH–) [37].…”
Section: Resultsmentioning
confidence: 99%
“…The N 1 s band was convoluted into two peaks at 399.1 and 398.35 eV, representing N–H and N–C, respectively. O 1 s XPS spectrum was decomposed into peaks at 530.6 and 529.5 eV, corresponding to O = C and O–C, respectively [ 49 ]. The spectrum of B 1 s exhibited two peaks at 190.8 and 190.2 eV, which could be assigned to B–C and B–O, respectively [ 42 ].…”
Section: Resultsmentioning
confidence: 99%