14.
"Biomimetic-dye affinity adsorbents for enzyme purification: application to the one-step purification of Candida boidinii formate dehydrogenase. "
N.E. Lambrou, A.D. Karagouni and Y.D. Klonis.
Biotechnology and Bioengineering,
vol. 48, pages 278-288, (1995).
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Abstract: Formate dehydrogenase (FDH, EC 1.2.1.2) was purified
from Candida boidinii cells in a single step by biomimetic-
dye affinity chromatography. For this purpose,
seven biomimetic analogues of the monochlorotriazine
dye, Cibacronm Blue 3GA (CB3GA), and parent dichlorotriazine
dye, Vilmafixa Blue A-R (VBAR), bearing a carboxylated
structure as their terminal biomimetic moiety,
were immobilized on crosslinked agarose gel, Ultrogelm
A6R. The corresponding new biomimetic-dye adsorbents,
along with nonbiomimetic adsorbents bearing
CB3GA and VBAR, were evaluated for their ability to purify
FDH from extracts obtained after press-disintegration
of C. boidinii cells. Optimal conditions for maximizing
specific activity of FDH in starting extracts (1.8 U/mg)
were realized when cell growth was performed on 4%
methanol, and press disintegration proceeded in four
consecutive passages before the homogenate was left to
stand for 1 h (4°C). When compared to nonbiomimetic
adsorbents, biomimetic adsorbents exhibited higher purifying
ability. Furthermore, one immobilized biomimetic
dye, bearing as its terminal biomimetic moiety mercaptopyruvic
acid linked on the chlorotriazine ring (BM6),
displayed the highest purifying ability. Adsorption equilibrium
data which were obtained for the BM6 adsorbent
in a batch system corresponded well to the Langmuir
isotherm and, in addition, breakthrough curves were
taken for protein and FDH adsorption in a fixed bed of
BM6 adsorbent. The dissociation constant (K,) of the
complex between immobilized BM6 and FDH was found
to equal 0.05 pM. Adsorbent BM6 was employed in the
purification of FDH from a 18-L culture of C. boidinii in a
single step (60% overall yield of FDH). The purified FDH
afforded a single-band on sodium dodecyl sulphate polyacrylamide
gel electrophoresis, and a specific activity of
7.0 U/mg (30°C).
13.
"The effect of soil moisture content on spore germination, mycelium development and survival of a seeded streptomycete in soil. "
A.D. Karagouni, A.P. Vionis, P.W. Baker and E.M.H. Wellington.
Microbial Releases,
vol. 2, pages 47-51, (1993).
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Abstract: No abstract available.
12.
"A continuous-culture approach to the analysis of inorganic carbon concentration by Synechococcus species. "
S. Bloye, A.D. Karagouni and N.G. Garr.
FEMS Microbiology Letters,
vol. 99, pages 79-84, (1992).
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Abstract: Chemostat cultures of Synechococcus PCC7942
were established in steady state over ten generations
with inorganic carbon-limiting biomass production.
The bicarbonate-concentration process
was not significantly induced; RuBisCo activity
was increased six-fold with decreasing dissolved
inorganic carbon concentration and the presence
of the 42-kDa cytoplasmic membrane polypeptide
was observed but not implicated in the process.
11.
"Isolation and identification of restriction endonuclease MspCI. "
M. Rina, M. Tzanodaskalaki, A. Karagouni, M. Pagomenou, I. Tsigos and V. Bouriotis.
Nucleic Acid Research,
vol. 20, pages 1806, (1992).
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Abstract: No abstract available.
10.
"Isolation and identification of restriction endonuclease SseBI. "
M. Rina, M. Tzanodaskalaki, A. Karagouni, M. Pagomenou, I. Tsigos and V. Bouriotis.
Nucleic Acid Research,
vol. 20, pages 1808, (1992).
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Abstract: No abstract available.
9.
"Isolation and identification of restriction endonuclease SseAI. "
M. Rina, A. Karagouni, M. Pagomenou, I. Tsigos and V. Bouriotis.
Nucleic Acid Research,
vol. 19, pages 6341, (1991).
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Abstract: No abstract available.
8.
"Isolation and identification of restriction endonuclease SgrBI. "
M. Rina, A. Karagouni, M. Pagomenou and V. Bouriotis.
Nucleic Acid Research,
vol. 19, pages 6342, (1991).
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Abstract: No abstract available.
7.
"Isolation and identification of restriction endonuclease BseBI. "
M. Rina, I. Tsigos, A. Karagouni, M. Pagomenou and V. Bouriotis.
Nucleic Acid Research,
vol. 19, pages 4776, (1991).
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Abstract: No abstract available.
6.
"The presence and absence of inorganic carbon concentration systems ιn unicellular cyanobacteria. "
A. D. Karagouni , S.A. Bloye and N. G. Garr.
FEMS Microbiology Letters,
vol. 68, pages 137–141, (1990).
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Abstract: The response of eight species of unicellular
cyanobacteria to growth under high and low CO2
regimes was measured by RuBisCO activity and
the extent of inorganic carbon concentration. No
significant increase in RuBisCO activity in CO 2-
limited batch cultures was observed. The main
feature of the data presented is the absence of a
bicarbonate concentrating process in the oceanic,
phycoerythrin-containing species examined, this is
discussed in light of bicarbonate supply in freshwater
and ocean environments.
5.
"Evidence that protein B of the thiosulfate-oxiding system of Thiobacillus versutus contains a binuclear manganese cluster. "
R. Cammacj, Karagouni , A. Chapman, W.P. Lu, A. Karagouni and D. P. Kelly.
FEBS Letters,
vol. 253, pages 239–243, (1989).
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Abstract: Manganese was shown to be an essential trace metal for growth and thiosulphate oxidation by Thiobacillus versutus in
chemostat culture. In the thiosulphate-oxidizing enzyme system of T. versutus, protein B was the only component found
to contain manganese in significant amounts. When it was examined by electron spin resonance (ESR) spectroscopy,
protein B gave a broad, complex spectrum, indicative of the presence of a dimeric manganese cluster, with manganese
in the Mn(II) oxidation state.
4.
"Carbon dioxide fixation by Thiobacillus versutus: apparent absence of a CO2-concentrating mechanism in organisms grown under carbon-limitation in the chemostat. "
A. D. Karagouni and D. P. Kelly.
FEMS Microbiology Letters,
vol. 58, pages 179–182, (1989).
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Abstract: Thiobacillus versutus responds to both CO 2-
1imitation and increase in chemostat dilution rate
under thiosulphate-limitation by increasing ribulose
bisphosphate carboxylase specific activity. It
has no high affinity CO2-concentrating mechanism
like that shown in Synechococcus, and may depend
on diffusional uptake of CO2/HCO3.
3.
"Screening of carob bean yeasts. Chemical composition of Schizosaccharomyces versatilis grown on aqueous carob extract"
S. G. Marakis and A. D. Karagouni.
Biotechnology Letters,
vol. 7, pages 831–836, (1985).
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Abstract: An improved extraction procedure for soluble sugars and tannins from
carob bean is described. The yeast flora of the carob is rich, with Saccharozyces
predominant; an isolate of Schizosaccharomyces versatilis cultured
in the aqueous extract utilizes tannins as well as sugars to give a high
biomass and protein yield of good quality.
2.
"Enzymes of the Calvin cycle and intermediary metabolism in the cyanobacterium Anacystis nidulans grown in chemostat culture"
A. D. Karagouni and J. H. Slater.
Journal of General Microbiology,
vol. 115, pages 369-376, (1992).
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Abstract: The cyanobacterium Anacystis nidulans grown in light-limited and CO2-limited chemostat cultures
showed varying rates of CO2 fixation with peaks at dilution rates of 0.10 to 0.12 h-1. The specific activities of a number of enzymes of the reductive and
oxidative pentose phosphate and glycolytic pathways and the tricarboxylic acid and glyoxylate cycles varied significantly as a function of the growth environment
(substrate limitation) and organism growth rate. Ribulose-1,5-bisphosphate carboxylase varied 15-fold under CO2-limited conditions but did not change under
light-limited conditions. With the exception of phosphoribulokinase, all enzymes which showed a change in specific activity increased with decreasing dilution rate.
The specific activities of glucose-6-phosphate dehydrogenase, 6-phosphogluconate dehydrogenase, hexokinase, ribulose-1,5-bisphosphate carboxylase and malate
dehydrogenase were significantly higher in organisms grown under CO2-limited conditions than under light-limited conditions. Fructose-1,6-bisphosphate aldolase
and phosphoribulokinase specific activities were similar at all growth rates and under both limitations. Isocitrate lyase was the only enzyme examined which showed
higher specific activities under light-limited conditions. Thus Anacystis nidulans can selectively express different enzymes, possibly by transcriptional control.
1.
"Growth of the blue-green alga Anacystis nidulans during washout from light-and carbon-limited chemostats"
A. D. Karagouni and J. H. Slater.
FEMS Microbiology Letters,
vol. 4, pages 295-299, (1978).
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Abstract: No abstract available