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.com

Volume 6, Issue 8 (Suppl)

J Biotechnol Biomater

ISSN: 2155-952X JBTBM, an open access journal

Bio America 2016

November 28-30, 2016

November 28-30, 2016 San Francisco, USA

13

th

Biotechnology Congress

Acceleration of glycolysis and D-lactate production by novel global metabolic engineering in yeast

Ryosuke Yamada, Kazuki Wakita

and

Hiroyasu Ogino

Osaka Prefecture University, Japan

T

he use of renewable feed-stocks for producing biofuels and bio-based chemicals by engineering metabolic pathways of yeast

Saccharomyces cerevisiae

has recently become an attractive option. Many researchers attempted to accelerate glycolysis by

over-expressing some glycolytic enzymes because most target bio-based chemicals are derived through glycolysis. However these

attempts have met with little success. In this study, to create a

S. cerevisiae

strain with high glycolytic flux, we used multi-copy

integration to develop a novel global metabolic engineering strategy. Then a novel global metabolic engineering strategy was applied

for D-lactate production. Among approximately 350 metabolically engineered strains, YPH499/dPdA3-34 exhibited the highest

glucose consumption rate. This strain showed 1.3-fold higher cell growth rate and glucose consumption rate than the control strain

YPH499/dPdAW. Real-time PCR analysis revealed that transcription levels of glycolysis-related genes such as

HXK2, PFK1, PFK2,

PYK2, PGI1

and

PGK1

in YPH499/dPdA3-34 were increased. Besides, by using global metabolic engineering strategy, D-lactate was

efficiently produced. This study successfully developed a novel global metabolic engineering strategy for

S. cerevisiae

, improving

glucose consumption rate through optimizing the expression of glycolysis-related enzymes. The method detailed here is a promising

approach to optimize

S. cerevisiae

metabolic pathways, thereby improving bio-based chemicals production using this organism.

Biography

Ryosuke Yamada has completed his PhD and Postdoctoral studies from Kobe University, Japan. He has then joined as an Assistant Professor at Osaka Prefecture

University, Japan. He has published more than 35 papers in journals related to applied microbiology and biochemical engineering.

yamada@chemeng.osakafu-u.ac.jp

Ryosuke Yamada et al., J Biotechnol Biomater 2016, 6:8(Suppl)

http://dx.doi.org/10.4172/2155-952X.C1.067