Biosynthesis approach

By using the biosynthesis approach, the shifts of the amide II and 0-H stretching peaks could indicate specific interactions between the functional groups of BC and gelatin [57]. 

Using the biosynthesis approach, a higher tensile strength, and Young s modulus of BC-chitosan composite were obtained by increasing the MW and concentration of chitosan. Because the fibrils became thicker, they could resist a stronger force than pure BC fibrils [19]. 

Sun X, Lin Y, Huang Q, Yuan Q, Yan Y. (2013). A novel muconic acid biosynthesis approach by shunting tryptophan biosynthesis via anthranilate. Appl Environ Microbiol, 79,4024-4 030. 

One of the lines of approach of such an investigation is the study of analogs of nucleic acid bases. The objective here is to prepare such analogs as would be incorporated into the nucleic acid molecules on the basis of their similarity to the natural species or as could interfere at some of the steps of nucleic acid biosynthesis. 

The tautomerization of porphyrinogens to pyrrocorphins has been reported in detail in connection with the synthesis of chlorins (sec Section 1.2.1.3.), baeteriochlorins (see Section 1.3.1.) and isobacteriochlorins (see Section 1.4.1.3.). Therefore, only the porphyrinogen-pyrrocorphin tautomerization of uroporphyrinogen I octacarbonitrile 8- 96 will be described as it is of importance regarding the biosynthesis and a possible prebiotic formation of corrins.la,b-2 A major problem concerned with using this approach synthetically is the number of possible diastereomeric products (4 in a 1 1 1 1 ratio) obtained in the reaction and also the formation of isobacteriochlorin diastereomers 10. 

The tetramerization of suitable monopyrroles is one of the simplest and most effective approaches to prepare porphyrins (see Section 1.1.1.1.). This approach, which is best carried out with a-(hydroxymethyl)- or ot-(aminomethyl)pyrroles, can be designated as a biomimetic synthesis because nature also uses the x-(aminomethyl)pyrrole porphobilinogen to produce uroporphyrinogen III. the key intermediate in the biosynthesis of all kinds of naturally occurring porphyrins, hydroporphyrins and corrins. The only restriction of this tetramerization method is the fact that tnonopyrroles with different -substituents form a mixture of four constitutionally isomeric porphyrins named as porphyrins I, II, III, and IV. In the porphyrin biosynthesis starting from porphobilinogen, which has an acetic acid and a propionic acid side chain in the y6-positions, this tetramerization is enzymatically controlled so that only the type III constitutional isomer is formed. 

Although a range of penicillins could be produced by directed biosynthesis using precursor feeding, this approach is limited by the toxicity of the precursors, the ability of the penicillin producing cells to take up the precursor and by the capability of the acyltransferase to transfer the acyl groups onto the 6-aminopenicillanic add moiety. 

An alternative strategy for producing new derivatives by directed biosynthesis is to produce mutants in which particular pathways may be blocked or a new pathway created. Again, we will use a specific example to illustrate this approach. 

A great deal has been learned about the biosynthesis of nitrogenases, but at the moment the process is understood only in broad outline. The detailed roles of the individual gene products require much further investigation, which may once more indicate fresh approaches to some of the problems identified herein. In particular, if the biosynthetic steps can be emulated chemically, then it may be possible to synthesize FeMoco in large quantities in order to allow its detailed analysis at the atomic level. 

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