Enzymatic methods solid-state

Biotechnological transformation is powerful tool to effectively utilize a broad variety of plant oils, with the aim to modify their structure for the production of new lipid-based materials with demanded properties and functions. One method of plant oil transformation is based on the direct utilization by microorganisms. Employed oils can be converted to aimed compounds by submerged cultivation or oils, and/or oleaginous plant materials can be utilized during solid state fermentation to useful bioproducts enriched with demanded microbial products. Another biotransformation technique covers the enzymatic modification of oil components to structured lipids with biological properties. 

The most important derivative of chitin is chitosan obtained by partial deacetylation of chitin in the solid state under alkaline conditions or by enzymatic hydrolysis in the presence of a chitin deacetylase. The ratio of 2-acetamido-2-deoxy-D-glucopyranose to 2-amino-2-deoxy-D-glucopyra-nose moieties determines the identity of the product, that is, chitin or chitosan [9]. The published methods used for the production of chitosan from chitin are summarized in Table 2.3. 

As discussed further in the following sections, there are other variations of rapid mixing/quench methods in which the enzymatic reaction is terminated by freezing the reaction mixture with liquid isopropane. The frozen sample is then analyzed hy electron paramagnetic resonance (EPR), solid-state NMR, or other spectroscopic techniques such as resonance Raman spectroscopy that can accommodate a solid sample. Perhaps the major limitation for implementation of this methodology is the sensitivity of the spectroscopic method and the requirement for large amounts of enzyme. ... 

Peptidylphosphonates have been demonstrated to mimic effectively the transition state involved in the enzymatic hydrolysis of the peptide bond, and are commonly used as inhibitors of peptidases, and in particular of metallo-proteases [146], A solid-phase method for the introduction of the (/[P0(0Me)0] motif exploits a modified Mitsunobu reaction (Scheme 7.11) [147]. 

---