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Novel hydrophilic NaYF4:Yb3+,Tm3+@NaGdF4:Ce3+,Eu3+ double-jacket microtubes (DJMTs) with upconversion/ downconversion dual-mode luminescence were designed and prepared through epitaxial growth of NaGdF4:Ce3+, Eu3+ shell onto the NaYF4:Yb3+,Tm3+ microtube via poly(acrylic acid) (PAA) mediated hydrothermal method. It is demonstrated that PAA ligand played an important role in guiding the direct growth of NaGdF4:Ce3+,Eu3+ shell onto the surface of NaYF4:Yb3+,Tm3+ parent microtubes. The growth of NaGdF4:Ce3+,Eu3+ shell experienced a crystal phase transition from β-NaGdF4 and β-NaYF4 mixture to β-NaYF4@NaGdF4 composite crystal, and morphology evolution from mixture of β-NaGdF4:Ce3+,Eu3+ nanorods and β-NaYF4:Yb3+,Tm3+ microtubes to NaYF4:Yb3+,Tm3+@NaGdF4: Ce3+,Eu3+ DJMTs. The formation mechanism of DJMTs was the dissolution−renucleation of β-NaGdF4:Ce3+,Eu3+ nanorods and the growth of β-NaGdF4:Ce3+,Eu3+ shell via the classical Ostwald ripening mechanism. The as-prepared DJMTs could exhibit blue upconversion and red downconversion luminescence, which was further made into environmentally benign luminescent inks for creating highly secured and fluorescent-based anti-counterfeiting patterns via inkjet printing.

Fusarium redolens Dzf2, an endophytic fungal species, is a high producer of the antibiotic compound beauvericin (BEA). However, the BEA produced by the F. redolens Dzf2 fungus was retained mainly as an intracellular product. This study was to evaluate an integrated fermentation-in situ product recovery process for enhancement of BEA production in F. redolens Dzf2 myelical culture. A macroporous polystyrene resin (X-5) was selected as the sorbent and added to the mycelial culture flasks (enclosed in a nylon bag). With 2 g resin added to 40 ml medium in each flask in the early stationary growth phase (day 5), the volumetric BEA yield (on day 7) was increased from 194 to 265 mg l −1 , with 65% being adsorbed to the resin phase. With resin renewal plus glucose feeding (on day 7), the BEA production was increased even more dramatically to 400 mg l −1 (on day 9), double of the yield in the batch control culture. The results show that in situ adsorption was an effective strategy for enhancing the BEA production and also facilitating its recovery in the mycelial liquid culture.