Carbon dioxide inhibition of yeast growth in biomass production

1976 ◽  
Vol 18 (10) ◽  
pp. 1455-1462 ◽  
Author(s):  
S. L. Chen ◽  
Feliks Gutmanis
2010 ◽  
Vol 56 (2) ◽  
pp. 128-137 ◽  
Author(s):  
D. Spadaro ◽  
A. Ciavorella ◽  
Z. Dianpeng ◽  
A. Garibaldi ◽  
M. L. Gullino

Few strains of Metschnikowia pulcherrima (Pitt) M.W. Miller are under development for control of postharvest pathogens on fruit. A substrate was developed to optimize the biomass production of M. pulcherrima strain BIO126. Different complex nutrient sources, with or without pH control, were tested. Growth in yeast extract provided at concentrations ≥30 g·L–1yielded the highest biomass. The addition of two carbon sources, d-mannitol and l-sorbose, at 5 g·L–1each, significantly improved yeast growth. The greatest amount of yeast growth occurred when pH values of the medium ranged from 5.0 to 7.5. A combination of yeast extract, d-mannitol, and l-sorbose (YEMS), probably with diauxic utilization, showed a synergistic effect, widening the exponential phase (maximum specific growth rate of 0.45 h–1) and increasing the final cell number (1.5 × 109cells·mL–1) and dry biomass (6.0 g·L–1) in well-controlled batch fermentation. In efficacy trials on ‘Golden Delicious’ apples, M. pulcherrima grown in YEMS effectively reduced incidence and severity of Botrytis cinerea (51.1% and 70.8%, respectively) and Penicillium expansum (41.7% and 14.0%, respectively). Also on ‘Gala’ apples, the best reduction of grey and blue mould incidence was obtained with cells grown in YEMS (58.1% and 50.5%, respectively).


Energy ◽  
2015 ◽  
Vol 89 ◽  
pp. 347-357 ◽  
Author(s):  
Bingtao Zhao ◽  
Yaxin Su ◽  
Yixin Zhang ◽  
Guomin Cui

2011 ◽  
Vol 102 (19) ◽  
pp. 9135-9142 ◽  
Author(s):  
Sheng-Yi Chiu ◽  
Chien-Ya Kao ◽  
Tzu-Ting Huang ◽  
Chia-Jung Lin ◽  
Seow-Chin Ong ◽  
...  

HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1151d-1151
Author(s):  
K.A. Corey ◽  
R.M. Wheeler ◽  
J.C. Sager ◽  
R.P. Prince

A wheat (Triticum aestivum cv. Yecora Rojo) stand was grown using nutrient film culture in the closed conditions of NASA's Biomass Production Chamber. Rates of photosynthesis and respiration of the entire stand (about 20 m2) were determined daily using a regime of 20 hr light/4 hr dark, 20 C light/16 C dark an average PPF of 600 μmol/m2/s from HPS lamps, and a CO2 cone of 1000 ppm. Fractional interception of PPF by the stand reached a maximum of 0.96 at 24 days from planting. Rates of photosynthesis were constant throughout the photoperiod as determined by short term drawdowns of CO2 throughout the photoperiod. Drawdown rates of CO2 were correlated with rates determined by logging of mass flow of CO2 injected during chamber closure. Photosynthetic drawdowns of CO2 indicated that photosynthesis was not saturated at 1000 ppm CO2 and that the CO2 compensation point was about 50 ppm. Whole stand light compensation points were 200 to 250 μmol/m2/s between days 13 and 70 and then increased rapidly during senescence.


2012 ◽  
Vol 1 (1) ◽  
pp. 10-14 ◽  
Author(s):  
H Hadiyanto ◽  
S Sumarno ◽  
Rufaida Nur Rostika ◽  
Noer Abyor Handayani

The biogas production from anaerobic digestion is a potential fuel for power generators application, if biogas can be upgraded to the same standards as fossil natural gas by CO2, H2S, and other non-combustible component removal. Microalgae Chlamydomonas sp. has potency to biofix the carbon dioxide and can be used as an additional food ingredient. The variations of flow rate and carbon dioxide concentration in the process resulting different value of biomass production and carbon dioxide biofixation. Biomass production at 40% carbon dioxide concentration obtained 5.685 gr/dm3 at 10% carbon dioxide concentration obtained 4.892 gr/dm3. The greatest value of carbon dioxide absorption occurs at a 40% concentration amounting to 12.09%. The rate of growth and productivity of microalgae tend to rise in 10% and 20% (%v) carbon dioxide concentration, but began started a constant at 30% and 40% (%v) carbon dioxide concentration. Biomass production tends to increase in light conditions while a constant in dark conditions. This study used Chlamydomonas sp. as media culture and performed on bubble column and tubular reactor with 6 litres of culture medium at a temperature of 28oC and atmospheric pressure.


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