182 - 186 |
Effects of fatty acid chain length and unsaturation number on triglyceride synthesis catalyzed by immobilized lipase in solvent-free medium Selmi B, Gontier E, Ergan F, Thomas D |
187 - 198 |
Estimation of the intracellular fluxes for a hybridoma cell line by material balances Paredes C, Sanfeliu A, Cardenas F, Cairo JJ, Godia F |
199 - 203 |
Reactivity of easily removable protecting groups for glycine in peptide synthesis using papain as catalyst Fite M, Alvaro G, Clapes P, Lopez-Santin J, Benaiges MD, Caminal G |
204 - 210 |
Simple two-step procedure for purification of cloned small sialidase from unclarified E-coli feedstocks Chang YK, Chen YH, Chien CH |
211 - 215 |
Lipase-catalyzed synthesis of peptides containing D-amino acid So JE, Kang SH, Kim BG |
216 - 226 |
Microbial transglutaminase production by Streptoverticillium mobaraense : Analysis of amino acid metabolism using mass balances Zhu Y, Rinzema A, Bonarius HPJ, Tramper J, Bol J |
227 - 242 |
Poly(vinyl alcohol) cryogels employed as matrices for cell immobilization. 3. Overview of recent research and developments Lozinsky VI, Plieva FM |
243 - 248 |
Protease-catalyzed synthesis of precursor dipeptides of RGD with reverse micelles Chen YX, Zhang XZ, Zheng K, Chen SM, Wang QC, Wu XX |
249 - 252 |
Increased production of alpha-amylase from Thermomyces lanuginosus by the addition of Tween 80 Arnesen S, Eriksen SH, Olsen J, Jensen B |
253 - 260 |
Terpene ester production in a solvent phase using a reverse micelle-encapsulated lipase Lee KKB, Poppenborg LH, Stuckey DC |
261 - 266 |
Decarboxylation of ferulic acid to 4-vinylguaiacol by Bacillus pumilus in aqueous-organic solvent two-phase systems Lee IY, Volm TG, Rosazza JPN |
267 - 273 |
Enhanced biosurfactant production by a Bacillus licheniformis mutant Lin SC, Lin KG, Lo CC, Lin YM |
274 - 280 |
Mechanism of removal of immobilized triacylglycerol by lipolytic enzymes in a sequential laundry wash process Flipsen JAC, Appel ACM, van der Hijden HTWM, Verrips CT |