scholarly journals Optimization of Corn Steep Liquor Dosage and Other Fermentation Parameters for Ethanol Production by Saccharomyces cerevisiae Type 1 and Anchor Instant Yeast

Energies ◽  
2018 ◽  
Vol 11 (7) ◽  
pp. 1740 ◽  
Author(s):  
Abiola Taiwo ◽  
Tafirenyika Madzimbamuto ◽  
Tunde Ojumu
2016 ◽  
Vol 6 (3-4) ◽  
pp. 219-234 ◽  
Author(s):  
Anh Huynh ◽  
Thomas Li ◽  
Mykola Kovalenko ◽  
Ryan D. Robinson ◽  
Alexander A. Fridman ◽  
...  

2015 ◽  
Vol 112 (7) ◽  
pp. 2222-2226 ◽  
Author(s):  
Timothy A. Kremer ◽  
Breah LaSarre ◽  
Amanda L. Posto ◽  
James B. McKinlay

A nascent cellulosic ethanol industry is struggling to become cost-competitive against corn ethanol and gasoline. Millions of dollars are spent on nitrogen supplements to make up for the low nitrogen content of the cellulosic feedstock. Here we show for the first time to our knowledge that the ethanol-producing bacterium,Zymomonas mobilis, can use N2gas in lieu of traditional nitrogen supplements. Despite being an electron-intensive process, N2fixation byZ. mobilisdid not divert electrons away from ethanol production, as the ethanol yield was greater than 97% of the theoretical maximum. In a defined medium,Z. mobilisproduced ethanol 50% faster per cell and generated half the unwanted biomass when supplied N2instead of ammonium. In a cellulosic feedstock-derived medium,Z. mobilisachieved a similar cell density and a slightly higher ethanol yield when supplied N2instead of the industrial nitrogen supplement, corn steep liquor. We estimate that N2-utilizingZ. mobiliscould save a cellulosic ethanol production facility more than $1 million/y.


2011 ◽  
Vol 102 (11) ◽  
pp. 6494-6501 ◽  
Author(s):  
Prasanth Maddipati ◽  
Hasan K. Atiyeh ◽  
Danielle D. Bellmer ◽  
Raymond L. Huhnke

1992 ◽  
Vol 42 (3) ◽  
pp. 191-195 ◽  
Author(s):  
A.I. El-Diwany ◽  
M.S. El-Abyad ◽  
A.H. El-Refai ◽  
L.A. Sallam ◽  
Reda F. Allam

2002 ◽  
Vol 68 (3) ◽  
pp. 1071-1081 ◽  
Author(s):  
S. A. Underwood ◽  
M. L. Buszko ◽  
K. T. Shanmugam ◽  
L. O. Ingram

ABSTRACT Previous studies have shown that high levels of complex nutrients (Luria broth or 5% corn steep liquor) were necessary for rapid ethanol production by the ethanologenic strain Escherichia coli KO11. Although this strain is prototrophic, cell density and ethanol production remained low in mineral salts media (10% xylose) unless complex nutrients were added. The basis for this nutrient requirement was identified as a regulatory problem created by metabolic engineering of an ethanol pathway. Cells must partition pyruvate between competing needs for biosynthesis and regeneration of NAD+. Expression of low-Km Zymomonas mobilis pdc (pyruvate decarboxylase) in KO11 reduced the flow of pyruvate carbon into native fermentation pathways as desired, but it also restricted the flow of carbon skeletons into the 2-ketoglutarate arm of the tricarboxylic acid pathway (biosynthesis). In mineral salts medium containing 1% corn steep liquor and 10% xylose, the detrimental effect of metabolic engineering was substantially reduced by addition of pyruvate. A similar benefit was also observed when acetaldehyde, 2-ketoglutarate, or glutamate was added. In E. coli, citrate synthase links the cellular abundance of NADH to the supply of 2-ketoglutarate for glutamate biosynthesis. This enzyme is allosterically regulated and inhibited by high NADH concentrations. In addition, citrate synthase catalyzes the first committed step in 2-ketoglutarate synthesis. Oxidation of NADH by added acetaldehyde (or pyruvate) would be expected to increase the activity of E. coli citrate synthase and direct more carbon into 2-ketoglutarate, and this may explain the stimulation of growth. This hypothesis was tested, in part, by cloning the Bacillus subtilis citZ gene encoding an NADH-insensitive citrate synthase. Expression of recombinant citZ in KO11 was accompanied by increases in cell growth and ethanol production, which substantially reduced the need for complex nutrients.


Sign in / Sign up

Export Citation Format

Share Document