There is increasing interest from many types of research groups in biocatalysis, in the application of enzymes which can replace chemical catalysts in synthetic processes, in the pharmaceutical and fine chemical industries.
The great potential of lipases has been known since 1930 when the work of J. B. S. Haldane was published.
Strem chemicals has a hugely growing portfolio of enzymes and Biocatalysts
Lipases (EC Number 18.104.22.168) are one of the most commonly used classes of enzymes in
biocatalysis. They have been used on a variety of substrates and show very broad substrate specificity. Lipases catalyse the hydrolysis of triacylglycerols to diacylglycerol,noacylglycerol, glycerol and free fatty acids. The reaction reverses under anhydrous conditions, and the enzyme can synthesize new molecules by esterification, alcoholysis, and transesterification. All reactions can be performed with high regio and enantioselectivity under mild reaction conditions and have a broad range of opportunities in process design.
We also have Immobilized Enzyme Kits Sold in collaboration with Purolite
Lipases are one of the most commonly used classes of enzymes in biocatalysis, while proteases have a broad range of opportunities in process design.
Novozymes’ Enzyme Screening Kits offer a fast, efficient way of easily accessing Novozymes’ portfolio of enzymes. Containing proven enzymes and lipase and protease enzymes used in the biocatalysis process that not only enable new, more sustainable routes for the production of intermediates and APIs, but offer commercial benefits such as better and more sustainable production, fewer side reactions and purification steps – all of which add up to lower costs, for the pharmaceutical and fine chemical specialist industries.
Using porphine derivative ligands for the preparation and functionalization of porphyrins
It is hard to overestimate the importance of porphyrins in life sciences. Chlorophylls, Vitamin B12 and haem (in haemoglobin) are just a few examples of how essential these naturally occurring materials are to life.
Many researchers have focused on synthetic metal porphyrins because of their outstanding properties such as chemical and structural stability, chromaticity, electronic and optical properties, strong aromaticity and rich metal coordination chemistry.
In general, simple metal porphyrins are prepared by the direct interaction of metal salts with corresponding porphyrin ligands. Single porphyrin units allow added functionalization and conjugation in arrays by using alkene or alkyne type linkers, resulting in delocalized electronic structures. This unique characteristic allows porphyrins to play an important role in photovoltaics as near infrared dyes, nonlinear optical materials, and electron-conducting molecular wires[1-2] to enzymatic porphyrins, such as Coproporphyrin and Uroporphyrin and TPP, metal complexes are very important materials for every kind of photochemical, electronic and optical applications (Organic and Polymer Light Emitting Diodes (OLED and PLED) as well as dye sensitisers (fluorescent dyes, etc.). Metal porphyrins typically exhibit two sets of absorption bands in the neighbourhood of 550 nm and 400 nm.
Metalloporphyrins are used as effective catalysts in almost every research discipline, such as organic chemistry, electro catalysis and biocatalysis to name a few. Porphyrin-ligands are also of interest in MOF technology, especially if porphyrin linkers are functionalized with carboxylic or pyridine groups in the outer sphere.
Porphyrins play an extremely important role in various biological systems in which they transport proteins, accept and donate electrons, and catalyse biochemical reactions. For instance, after a series of reactions, uroporphyrinogen and coproporphyrinogen in the body will automatically oxidize to uroporphyrin 07-3350 CAS 10170-03-3 and 07-3410 CAS 15435-60-6
In the Coproporphyrin I isomer 07-0300 CAS 69477-27-6, the four propionic acid side groups are equidistant and the molecule is thus symmetric. In the Coproporphyrin III isomer 07-0305 CAS 14643-66-4 one of the pyrroles is inverted during the biosynthesis of the porphyrin ring structure, resulting in an asymmetric distribution of methyl and propionic acid side groups of the porphyrin molecule.