Savas Anastassiadis
Democritus University of Thrace
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Featured researches published by Savas Anastassiadis.
Electronic Journal of Biotechnology | 2006
Savas Anastassiadis; Hans-Jürgen Rehm
The effect of air saturation on citric acid production in batch, repeated batch and chemostat cultures has been studied. It was shown that, under continuous fermentation (chemostat mode), the highest concentration of citric acid equal of 98 g/l was produced at 20% of air saturation. In contrary to continuous fermentation, displaying an optimum at 20%, 80% air saturation yielded higher values in repeated batch fermentation process. 167 g/l citric acid were produced continuously with the fill and drain technique at 4.85 days, at 80% air saturation, compared with 157.6 g/l achieved within 5.4 days at 20%. Under repeated batch fermentation, the formation rate of the generic product (Rj) as well as the specific citric acid productivity (m p ) reached a maximum of 1.283 g/(l x hr) at 4.01 days and of 0.0375 g/(g x hr) at 4.58 days, respectively. The glucose consumption rate (Rx) reached a maximum value of 3.33 g/(l x hr) entering stationary phase after 2.56 days at a glucose concentration of 131.2 g/l.
Electronic Journal of Biotechnology | 2005
Savas Anastassiadis; Hans-Jürgen Rehm
Financial support: Part of the work that has been carried out at the Institute of Biotechnology 2 of Research Centre Julich (Germany) was financed by Haarmann and Reimer, a daughter company of the company Bayer, Leverkusen, Germany.
Electronic Journal of Biotechnology | 2006
Savas Anastassiadis; Hans-Jürgen Rehm
The influence of air saturation and temperature on continuous citric acid secretion was studied in chemostat cultures of Candida oleophila ATCC 20177 (var.). Simultaneous measurements of intra- and extracellular concentration of glucose, citric and isocitric acid confirmed the involvement of a specific active transport system in citrate secretion, favouring citric acid over isocitrate. An optimum air oxygen saturation of 20% and temperature of 30-31oC were determined for the continuous citric acid secretion. The highest values of citric acid concentration (98 g/L), citrate to isocitrate ratio (33.3:1), volumetric citric productivity (1.8 g/(L x h)), and specific citric acid productivity (0.1 g/(g x h)), were reached at 20% air saturation at a residence time of 54 hrs by the experiments lowest biomass of 18 g/L. The highest isocitic acid volumetric productivity (55.6 mg/(L x h)) and specific productivity (0.99 mg/(g x h)) were identified at 50%, instead. The fastest citrate excretion rate of the generic product of 0.046 g/(g*h) was found at 30-31oC. A concentration ratio between extra- and intracellular concentration of citrate of up to 9 was identified. The highest extra-/intracellular ratio of citrate and lowest intracellular concentrations of glucose, citric and isocitric acid were determined at optimum air saturation as a consequence of active citrate export.
Electronic Journal of Biotechnology | 2006
Savas Anastassiadis; Hans-Jürgen Rehm
New alternative processes for the continuous production of gluconic acid by Aureobasidium pullulans , using biomass retention by cell immobilization or cross over filtration, are described in the present work. 315 g/l gluconic acid was continuously produced in chemostat cultures at 21 hrs residence time without any biomass retention. 260 g/l gluconic acid was produced in fluidized bed reactor at 21 hrs residence time. The support carrier was overgrown resulting in limitations of oxygen transfer towards the inner layers of immobilized biomass. 375 g/l gluconic acid was produced under continuous cultivation at 22 hrs of residence time with a formation rate for the generic product of 17 g/(l x h) and a specific gluconic acid productivity of only 0.74 g/(g x h), using biomass retention by cross over filtration. 370 g/l were obtained at 19 hrs RT and 100% conversion with 25 g/l biomass and a formation rate of 19 g/(l x h). At 100% conversion, a selectivity of only 78% was determined at 22 hrs and of 77% at 19 hrs RT, because of the very high biomass concentration. Biomass retention makes it possible to break the existing link between growth and residence time.
The Open Biotechnology Journal | 2008
Savas Anastassiadis; Svetlana V. Kamzolova; Igor G. Morgunov; Hans-Jürgen Rehm
New processes have been previously described for the continuous and discontinuous production of gluconic acid by Aureobasidium pullulans (de bary) Arnaud. Little is known about the regulatory mechanisms of gluconic acid production by A. pullulans. The response of growth and gluconic acid metabolism to a variable profile of iron concentra- tions was studied with A. pullulans in batch and chemostat cultures. A surprisingly high optimum N-dependent iron ion concentration in the feed medium, in the range between 0.5 mM and 3.0 mM Fe (optimum 1-2 mM), was found to be par- ticular requirement for economically profitable continuous production of gluconic acid with 3 g/l NH4Cl. Increased iron concentration promoted growth on defined glucose medium. 223.3 g/l gluconic acid were continuously produced at a for- mation rate of the generic product (Rj) of 16.8 g/(l h) and a specific gluconic acid productivity (mp) of 2.5 g/(g h) at 13 h residence time (RT) with 1mM iron, compared with 182 g/l reached at 0.1 mM. The product selectivity (product yield based on glucose) increased continuously by raising iron concentration following a saturation curve, reaching a maximum of about 98% (mol/mol) at 2 mM Fe and 76.2% conversion, compared with only 84.3% determined at 0.1 mM. The proc- ess is not obligatory growth limiting or growth related and residual nitrogen was found in all of continuous experiments, e.g. 197 mg/l of nitrogen at 0.1 mM and 201 mg/l at 2 mM of iron.
Applied Microbiology and Biotechnology | 2002
Savas Anastassiadis; Alexander Aivasidis; Christian Wandrey
Food Technology and Biotechnology | 2011
Svetlana V. Kamzolova; Alina R. Fatykhova; E. G. Dedyukhina; Savas Anastassiadis; Nikolay P. Golovchenko; Igor G. Morgunov
Applied Microbiology and Biotechnology | 2003
Savas Anastassiadis; Alexander Aivasidis; Christian Wandrey
Biotechnology and Bioengineering | 2005
Savas Anastassiadis; Alexander Aivasidis; Christian Wandrey; Hans-Jürgen Rehm
World Journal of Microbiology & Biotechnology | 2005
Savas Anastassiadis; C. Wandrey; Hans-Jürgen Rehm