Nature provides an almost limitless supply of sources that inspire scientists to develop new materials with novel applications and less of an environmental impact. Recently, much attention has been focused on preparing natural‐product‐derived carbon dots (NCDs), because natural products have several advantages. First, natural products are renewable and have good biocompatibility. Second, natural products contain heteroatoms, which facilitate the fabrication of heteroatom‐doped NCDs without the addition of an external heteroatom source. Finally, some natural products can be used to prepare NCDs in ways that are very green and simple relative to traditional methods for the preparation of carbon dots from man‐made carbon sources. NCDs have shown tremendous potential in many fields, including biosensing, bioimaging, optoelectronics, and photocatalysis. This Review addresses recent progress in the synthesis, properties, and applications of NCDs. The challenges and future direction of research on NCD‐based materials in this booming field are also discussed.

A simple and flexible approach is developed for controllable fabrication of spider-silk-like microfibers with tunable magnetic spindle-knots from biocompatible calcium alginate for controlled 3D assembly and water collection. Liquid jet templates with volatile oil drops containing magnetic Fe3O4 nanoparticles are generated from microfluidics for fabricating spider-silk-like microfibers. The structure of jet templates can be precisely adjusted by simply changing the flow rates to tailor the structures of the resultant spider-silk-like microfibers. The microfibers can be well manipulated by external magnetic fields for controllably moving, and patterning and assembling into different 2D and 3D structures. Moreover, the dehydrated spider-silk-like microfibers, with magnetic spindle-knots for collecting water drops, can be controllably assembled into spider-web-like structures for excellent water collection. These spider-silk-like microfibers are promising as functional building blocks for engineering complex 3D scaffolds for water collection, cell culture, and tissue engineering.

Ectoine and hydroxyectoine as typical representatives of compatible solutes are not only essential for extremophiles to survive in extreme environments, but also widely used in cosmetic and medical industries. Ectoine was traditionally produced by Halomonas elongata through a “bacterial milking” process, of which the marked feature is using a high-salt medium to stimulate ectoine biosynthesis and then excreting ectoine into a low-salt medium by osmotic shock. The optimal hydroxyectoine production was achieved by optimizing the fermentation process of Halomonas salina. However, high-salinity broth exacerbates the corrosion to fermenters, and more importantly, brings a big challenge to the subsequent wastewater treatment. Therefore, increasing attention has been paid to reducing the salinity of the fermentation broth but without a sacrifice of ectoine/hydroxyectoine production. With the fast development of functional genomics and synthetic biology, quite a lot of progress on the bioproduction of ectoine/hydroxyectoine has been achieved in recent years. The importation and expression of an ectoine producing pathway in a non-halophilic chassis has so far achieved the highest titer of ectoine (~ 65 g/L), while rational flux-tuning of halophilic chassis represents a promising strategy for the next-generation of ectoine industrial production. However, efficient conversion of ectoine to hydroxyectoine, which could benefit from a clearer understanding of the ectoine hydroxylase, is still a challenge to date.

Using fluorescent materials to improve solar energy capture by chloroplasts has the potential to significantly enhance natural photosynthesis. Most currently available fluorescent materials, however, are derived from unsustainable petroleum resources and suffer from aggregation-caused quenching, both of which limit their practical application. Here, we used nanotechnology to engineer a hybrid photosynthesis system, comprising natural photosynthetic chloroplasts and aggregation-induced emission carbon dots (CD-AIEgens) made from natural quercetin. The CD-AIEgens possess unique optical properties, including AIE active fluorescence, efficient harvesting of ultraviolet light, and good photostability. Since the CD-AIEgens are able to harvest solar energy over a wider range of wavelengths than natural chloroplasts, by coating chloroplasts with CD-AIEgens, we were able to produce a new type of bio-based optical hybrid (chloroplasts/CD-AIEgens complexes) with increased photosynthetic efficiency. In addition to capturing a broader range of light, chloroplasts/CD-AIEgens complexes can accelerate electron transport rates in photosystem II, the critical protein complex in chloroplasts, and augment photosynthesis beyond that of natural chloroplasts. In this study, we developed an easily prepared nanoengineering strategy to enhance solar energy conversion by chloroplasts using light-harvesting-sustainable carbon dots.

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A novel type of smart microspheres with K(+)-induced shrinking and aggregating properties is designed and developed on the basis of a K(+)-recognition host-guest system. The microspheres are composed of cross-linked poly(N-isopropylacrylamide-co-acryloylamidobenzo-15-crown-5) (P(NIPAM-co-AAB15C5)) networks. Due to the formation of stable 2:1 "sandwich-type" host-guest complexes between 15-crown-5 units and K(+) ions, the P(NIPAM-co-AAB15C5) microspheres significantly exhibit isothermally and synchronously K(+)-induced shrinking and aggregating properties at a low K(+) concentration, while other cations (e.g., Na(+), H(+), NH4(+), Mg(2+), or Ca(2+)) cannot trigger such response behaviors. Effects of chemical compositions of microspheres on the K(+)-induced shrinking and aggregating behaviors are investigated systematically. The K(+)-induced aggregating sensitivity of the P(NIPAM-co-AAB15C5) microspheres can be enhanced by increasing the content of crown ether units in the polymeric networks; however, it is nearly not influenced by varying the monomer and cross-linker concentrations in the microsphere preparation. State diagrams of the dispersed-to-aggregated transformation of P(NIPAM-co-AAB15C5) microspheres in aqueous solutions as a function of temperature and K(+) concentration are constructed, which provide valuable information for tuning the dispersed/aggregated states of microspheres by varying environmental K(+) concentration and temperature. The microspheres with synchronously K(+)-induced shrinking and aggregating properties proposed in this study provide a brand-new model for designing novel targeted drug delivery systems.

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