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Biotechnology and Bioengineering|August 16, 2001
Utilizing genetically engineered bacteria to produce plant-specific glucosidesJ Arend, H Warzecha, T Hefner, et al.Biotechnology and Bioengineering|April 1, 1977
SCP production by Chaetomium cellulolyticum, a new thermotolerant cellulolytic fungusM Moo-Young, D S Chahal, J E Swan, et al.Biotechnology and Bioengineering|July 1, 1977
Characteristics of unbuffered gel-immobilized urease particles. II. Overall rate of reactionB Atkinson, I RousseauBiotechnology and Bioengineering|August 1, 1977
Competition for mixed substrates by microbial populationsH Yoon, G Klinzing, H W BlanchBiotechnology and Bioengineering|November 25, 2016
In vitro suppression of two different stop codonsEden Ozer, Yonatan Chemla, Orr Schlesinger, et al.Biotechnology and Bioengineering|November 25, 2016
Maximization of cell viability rather than biocatalyst activity improves whole-cell ω-oxyfunctionalization performanceMarvin Kadisch, Mattijs K Julsing, Manfred Schrewe, et al.Biotechnology and Bioengineering|November 19, 2016
Challenges in engineering large customized bone constructsDavid P Forrestal, Travis J Klein, Maria A WoodruffBiotechnology and Bioengineering|November 19, 2016
Omega-3 production by fermentation of Yarrowia lipolytica: From fed-batch to continuousDongming Xie, Edward Miller, Pamela Sharpe, et al.Biotechnology and Bioengineering|November 22, 2016
Integration of parallel 13 C-labeling experiments and in silico pathway analysis for enhanced production of ascomycinHaishan Qi, Mengmeng Lv, Kejing Song, et al.Biotechnology and Bioengineering|May 3, 2014
NADH plays the vital role for chiral pure D-(-)-2,3-butanediol production in Bacillus subtilis under limited oxygen conditionsJing Fu, Zhiwen Wang, Tao Chen, et al.Pageof 1,376