Titlebook: Metabolic Engineering; Jens Nielsen,L. Eggeling,W. H. Zyl Book 2001 Springer-Verlag Berlin Heidelberg 2001 Amino acid.Biochemical Engineer

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書目名稱Metabolic Engineering影響因子(影響力)




書目名稱Metabolic Engineering影響因子(影響力)學(xué)科排名




書目名稱Metabolic Engineering網(wǎng)絡(luò)公開度




書目名稱Metabolic Engineering網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Metabolic Engineering被引頻次




書目名稱Metabolic Engineering被引頻次學(xué)科排名




書目名稱Metabolic Engineering年度引用




書目名稱Metabolic Engineering年度引用學(xué)科排名




書目名稱Metabolic Engineering讀者反饋




書目名稱Metabolic Engineering讀者反饋學(xué)科排名

Agility

Jens Nielsen,L. Eggeling,W. H. ZylThis review series covers trends in modern biology.All aspects of this interdisciplinary technology, where knowledge, methods and expertise are required from chemistry, biochemistry, microbiology, gen

Pcos971

Advances in Biochemical Engineering/Biotechnologyhttp://image.papertrans.cn/m/image/631232.jpg

sulcus

978-3-642-07534-6Springer-Verlag Berlin Heidelberg 2001

CRAMP

Metabolic Engineering978-3-540-45300-0Series ISSN 0724-6145 Series E-ISSN 1616-8542

Nefarious

Gregory Stephanopoulos,Ryan T. Gillds; but our goal is not to present them in general, we want to develop all these notions and results in dimension 2. We would like this book to be a nice introduction to the qualitative theory of di?erential equations in the plane, providing simultaneously the major part of concepts and ideas for de

AWL

Daniel E. Stafford,Kurt S. Yanagimachi,Gregory Stephanopoulosds; but our goal is not to present them in general, we want to develop all these notions and results in dimension 2. We would like this book to be a nice introduction to the qualitative theory of di?erential equations in the plane, providing simultaneously the major part of concepts and ideas for de

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漂亮才會(huì)豪華

0724-6145 and in the engineering of .S. cerevisiae. for xylose metabolism, and the improvement of a complex biotransformation process.978-3-642-07534-6978-3-540-45300-0Series ISSN 0724-6145 Series E-ISSN 1616-8542

發(fā)展

Metabolic Engineering of Indene Bioconversion in , sp.,teady state metabolite balancing and labeling with [.C]-tracers revealed that at least 94% of the indene is oxidized by a monooxygenase to indan oxide that is subsequently hydrolyzed to .-(1.,2.)-indandiol and .-(1.,2.)-indandiol. This analysis identified several targets in KY1 for increasing (2.)-i