Pigmentation of wheat grain and coleoptile is controlled by the R gene on chromosomes of the homoeologous group 3 and the Rc gene on chromosomes of the homoeologous group 7, respectively. Each of these genes is inherited monogenically. The pigment of grain has been suggested to be a derivative of catechin-tannin and that of coleoptile to be anthocyanin. These polyphenol compounds are known to be synthesized through the flavonoid biosynthesis pathway. We isolated 4 partial nucleotide sequences of the early flavonoid biosynthesis genes (CHS, CHI, F3H, and DFR) in wheat. The expression of these genes was examined in the developing grain of red-grained and white-grained wheat lines. CHS, CHI, F3H, and DFR were highly upregulated in the grain coat tissue of the red-grained lines, whereas there was no significant expression in the white-grained lines. These results indicate that the R gene is involved in the activation of the early flavonoid biosynthesis genes. As for coleoptile pigmentation, all 4 genes were expressed in the red coleoptile; however, DFR was not activated in the white coleoptile. The Rc gene appears to be involved in DFR expression. The possibility that wheat R and Rc genes might be transcription factors is discussed.

Paired electrolysis is highly valuable from the viewpoint of efficiency as well as atom and energy economies. In order to optimize the latter two for chemical reactions, the development of paired electrochemical processes is necessary. When both of the electrodes in an electrochemical cell (divided and undivided) are applied as working electrodes, and both sides of the processes (oxidation and reduction) yield valuable compounds, this ideal electrolysis phenomena is defined as paired electrosynthesis. This paired electrolysis offers the opportunity to reduce the spent energy and time, when compared with a single electrolysis system that is only used to achieve a product of interest, while ignoring the other side of the electrolysis (anodic or cathodic). In an ideal case, 200% current efficiency could be achieved during paired electrosynthesis using cathodic and anodic processes to provide the same product. Paired electrosynthesis is a highly efficient green process and, therefore, is beneficial for preserving resources and minimizing waste. However, while a paired electrosynthesis is beneficial, both oxidation and reduction processes must be compatible to counter the yield losses and equally ease separation and purification of both sides of the electrode products. Greater efforts are required to perform paired electrosynthesis with a more systematic and rational approach to achieve optimal products under paired conditions. Nevertheless, new computational tools could be applied for assistance in this matter. There is a considerable level of adventure in designing new paired electrosynthetic processes and accompanying opportunities to design innovative and powerful synthetic strategies. Herein, an overview of several examples of paired electrosyntheses and their advantages are summarized that will aid researchers to both develop a greater understanding of this subject and subsequently employ paired electrolysis for green and sustainable synthesis of organic molecules.

A water-soluble imidazolium-based fluorescent chemosensor senses RNA selectively through fluorescence enhancement over other biologically relevant biomolecules in aqueous solution at physiological pH 7.4. Fluorescence image detection of RNA in living cells such as onion cells, HeLa cells, and animal model cells was successfully demonstrated which displays a chelation-enhanced fluorescence effect. These affinities can be attributed to the strong electrostatic (C-H)(+)···A(-) ionic H-bonding and the aromatic moiety driven π-stacking of imidazolium-based cyclophane with the size-complementary major groove of RNA.

Herein, electrochemical annulations involving mediators and mediator-free conditions have been discussed. Also, the use of sacrificial electrodes has been explored.