Functional π-Gelators and Their Applications

In the year 2003 there was a 17% increase in the number of publications citing work performed using optical biosensor technology compared with the previous year. We collated the 962 total papers for 2003, identified the geographical regions where the work was performed, highlighted the instrument types on which it was carried out, and segregated the papers by biological system. In this overview, we spotlight 13 papers that should be on everyone's 'must read' list for 2003 and provide examples of how to identify and interpret high-quality biosensor data. Although we still find that the literature is replete with poorly performed experiments, over-interpreted results and a general lack of understanding of data analysis, we are optimistic that these shortcomings will be addressed as biosensor technology continues to mature.

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmr.753

Survey of the year 2003 commercial optical biosensor literature

Studies of steroid modifications catalyzed by microbial whole cells represent a well-established research area in white biotechnology. Still, advances over the last decade in genetic and metabolic engineering, whole-cell biocatalysis in non-conventional media, and process monitoring raised research in this field to a new level. This review summarizes the data on microbial steroid conversion obtained since 2003. The key reactions of structural steroid functionalization by microorganisms are highlighted including sterol side-chain degradation, hydroxylation at various positions of the steroid core, and redox reactions. We also describe methods for enhancement of bioprocess productivity, selectivity of target reactions, and application of microbial transformations for production of valuable pharmaceutical ingredients and precursors. Challenges and prospects of whole-cell biocatalysis applications in steroid industry are discussed.

Microbial steroid transformations: current state and prospects

The report contains an overview of methods available for asymmetric preparation of a range of 1H- aziridines and their N-substituted analogues

The asymmetric synthesis of aziridines

Publisher Summary This chapter discusses the composition of reducing sugars in solution. Reducing sugars differ from most other organic compounds in one characteristic property. When a pure organic compound that is not a reducing sugar is dissolved in a solvent, it is certain that the solution will usually contain only one compound; but when a reducing sugar, above an aldotetrose or a 2-pentulose, is dissolved in water, a solution is obtained that always contains at least six compounds: two pyranoses, two furanoses, and an acyclic (open-chain) carbonyl form and its hydrate. There are also minute proportions of septanoses and dimers. Very few of these many compounds that are present in the equilibrium solutions of sugars have ever been isolated. The only method for separating them from the equilibrium mixture is by crystallization and that depends on the fortuitous presence of seed crystals. The chapter details about the pyranose form, the furanose form, and the septanose form. It also discusses the composition of aldoses, ketoses, and substituted and derived sugars in aqueous solution.

The composition of reducing sugars in solution

A new saccharide receptor in protic media has been designed and synthesized. The receptor combines advantages of steroids, which are responsible for saccharide binding, and of the porphyrin moiety acting as a signalling component of the molecule due to changes in UV-vis electronic spectra. The synthesis is based on condensation of steroid aldehyde with pyrrole to form the porphyrin unit with four protected steroid moieties. After deprotection, meso-substituted porphyrin contains 12-hydroxy groups on the steroidal part. The receptor is soluble in aqueous solutions and exhibits high complexation affinity towards saccharides. Because the receptor extensively aggregates in water, most of the experiments were performed in 50% aqueous 2-propanol where aggregation is significantly eliminated. Binding is evidenced by spectral changes in the Soret region of the receptor in UV-vis absorption spectra allowing the evaluation of the binding constants. Additional confirmation of binding is obtained using 1H NMR, Raman and IR spectroscopies and the surface plasmon resonance technique. The receptor exhibits higher selectivity for oligosaccharides over monosaccharide. The results point to the importance of a combination of multiple binding via H-bonding and hydrophobic interactions.

Steroid–porphyrin conjugate for saccharide sensing in protic media

Altered profiles of serum neuroactive steroids in premenopausal women treated for alcohol addiction

Metal coordination as a tool for controlling the self-assembling and gelation properties of novel type cholic amide–phenanthroline gelating agent

Stereoselectivity of sodium borohydride reduction of saturated steroidal ketones utilizing conditions of Luche reduction.

http://directory.umm.ac.id/Data%20Elmu/jurnal/P/PlantScience/PlantScience_Elsevier/Vol148.Issue2.2000/5186.pdf

Ivan Černý

Papers

Steroid–porphyrin conjugate for saccharide sensing in protic media

Altered profiles of serum neuroactive steroids in premenopausal women treated for alcohol addiction

Metal coordination as a tool for controlling the self-assembling and gelation properties of novel type cholic amide–phenanthroline gelating agent

Stereoselectivity of sodium borohydride reduction of saturated steroidal ketones utilizing conditions of Luche reduction.

Immunoanalysis of isoflavonoids in Pisum sativum and Vigna radiata