Enzymatic synthesis of structured triacylglycerols (sTAGs) highly rich in palmitic acid at position 2 and caprylic acid at positions 1 and 3
✍ Scribed by M.J. Jiménez; L. Esteban; A. Robles; E. Hita; L. Martín; A. Rodriguez; P.A. González; E. Molina
- Publisher
- Elsevier
- Year
- 2009
- Tongue
- English
- Weight
- 81 KB
- Volume
- 25
- Category
- Article
- ISSN
- 1871-6784
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✦ Synopsis
used as sulfur model compound at a initial constant concentration of 25 M. To determine the components evolution during BDS, a previously developed HPLC-UV-diode-array analytical technique was employed to analyze the evolution of all the intermediates of 4S route.
Experimental results show different influences on biodesulfurization capability of DBT due both to the cosubstrate employed and the concentration of it. BDS is able to be improved by adding cosubstrates till a 80%.
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## Abstract Peptide β‐hairpin formation is facilitated by centrally positioned D‐Pro‐Xxx segments. The synthetic peptides Boc‐Leu‐Phe‐Val‐D‐Pro‐Ac~6~c‐Leu‐Phe‐Val‐OMe (**1**) and Boc‐Leu‐Phe‐Val‐D‐Pro‐Ac~8~c‐Leu‐Phe‐Val‐OMe (**2**) were synthesized in order to explore the role of bulky 1‐aminocyclo