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1.
Silva Daniel Pereira Pessoa Adalberto Roberto Inês-Conceição Vitolo Michele 《Applied biochemistry and biotechnology》2001,91(1-9):605-613
A batch culture of Saccharomyces cerevisiae for the production of hexokinase was carried out in a 5-L fermentor containing 3 L of culture medium, which was in oculated
with cell suspension (about 0.7 g/L), and left ferm entingat 35°C and pH 4.0. The aeration and agitation were adjusted to
attain k
La values of 15, 60, 135, and 230 h−1. The highest hexokinase productivity (754.6 U/[L h]) and substrate-cell conversion yield (0.21 g/g) occurred for a k
La of 60 h−1. Moreover, the formation of hexokinase and cell growth are coupled events, which is in accordance with the constitutive character
of this enzyme. Hexokinase formation for k
La>60 h−1 was not enhanced probably owing to saturation of the respiratory pathway by oxygen. 相似文献
2.
Jinzhang Gao Jing Liu Jie Ren Xiuli Niu Yingying Zhang Wu Yang 《Central European Journal of Chemistry》2009,7(3):298-302
This paper described the determination of p-nitroaniline in a double organic substrate oscillating system of tartrate-acetone-Mn2+-KBrO3-H2SO4. Under the optimum conditions, temperature was chosen as a control parameter to design the bifurcation point and proposed
a convenient method for determination of p-nitroaniline. Results showed that the system consisting of 3.5 mL 0.06 mol L−1 tartrate, 4.0 mL 0.7 mol L−1 H2SO4, 1.5 mL 1.5×10−4 mol L−1 MnSO4, 4.0 mL 0.4 mol L−1 acetone and 7.0 mL 0.05 mol L−1 KBrO3 was very sensitive to the surrounding at 33.5°C. A good linear relationship between the potential difference and the negative
logarithm concentration of p-nitroaniline was obtained to be in the range of 2.50×10−7∼3.75×10−5 mol L−1 with a lower detection limit of 2.50×10−8 mol L−1.
相似文献
3.
A square wave voltammetric method whith a static mercury drop electrode (SMDE) was developed for the quantitative determination
of iron (III) in Zn-Fe alloy galvanic baths. Real alloy bath samples were analyzed by the standard addition method and recovery
tests were carried out. 0.50 mol L–1 sodium citrate (pH 6.0) or 0.20 mol L–1 oxalic acid (pH 4.0) were applied as supporting electrolytes resulting in both cases in a peak potential of about –0.20 V
vs. Ag|AgCl (saturated KCl). The iron (III) concentration in the alloy bath was 9.0 × 10–4 mol L–1. A good correlation (r = 0.9999) was achieved between the iron (III) concentration and the peak current in the electrolytes
studied, with linear response ranges from 1.0 × 10–6 to 1.2 × 10–4 mol L–1. Interference levels for some metals such as copper (II), lead (II), chromium (III) and manganese (II) that can hinder the
Zn-Fe alloy deposition were evaluated; only copper (II) interferes seriously.
Received: 4 April 2000 / Revised: 19 June 2000 / Accepted: 22 June 2000 相似文献
4.
Faria Luis F. Figueiredo Gimenes Maria Antonieta P. Nobrega Ronaldo Pereira Nei 《Applied biochemistry and biotechnology》2002,98(1-9):449-458
Oxygen availability is the most important environmental parameter in the production of xylitol by yeasts, directly affecting
yields and volumetric productivity. This work evaluated the cell behavior in fermentations carried out with different dissolved
oxygen concentrations (0.5–30.0% of saturation), as well as a limited oxygen restriction (0% of saturation), at several oxygen
volumetric transfer coefficients (12 ≤ k
L
a ≤ 70 h−1). These experiments allowed us to establish the specific oxygen uptake rate limits to ensure high yields and volumetric productivity.
When oxygen availability was limited, the specific oxygen uptake rate values were between 12 and 26 mg of O2/of g cell·h, resulting in a yield of 0.71 g of xylitol/xylose consumed, and 0.85 g/[L·h] for the volumetric productivity.
According to the results, the effective control of the specific oxygen uptake rate makes it possible to establish complete
control over this fermentative process, for both cell growth and xylitol production. 相似文献
5.
The simultaneous determination of three isomers of phenylenediamines (o, m, and p-phenylenediamine) and two isomers of dihydroxybenzenes (catechol and resorcinol) in hair dyes was performed by capillary
zone electrophoresis coupled with amperometric detection (CZE–AD). The effects of working electrode potential, pH and concentration
of running buffer, separation voltage, and injection time on CZE–AD were investigated. Under the optimum conditions the five
analytes could be perfectly separated in 0.30 mol L−1 borate–0.40 mol L−1 phosphate buffer (pH 5.8) within 15 min. A 300 μm diameter platinum electrode had good responses at +0.85 V (versus SCE)
for the five analytes. Their linear ranges were from 1.0 × 10−6 to 1.0 × 10−4 mol L−1 and the detection limits were as low as 10−7 mol L−1 (S/N = 3). This working electrode was successfully used to analyze eight kinds of hair dye sample with recoveries in the range
91.0–108.0% and RSDs less than 5.0%. These results demonstrated that capillary zone electrophoresis coupled with electrochemical
detection using a platinum working electrode as detector was convenient, highly sensitive, highly repeatable and could be
used in the rapid determination of practical samples.
Figure Electropherograms obtained from 10 mg mL−1 hair dye sample solutions at a platinum working electrode under optimum CZE–AD conditions: (a) natural black (I), (b) golden: (1) p-phenylenediamine, (2) m-phenylenediamine, (3) o-phenylenediamine, (4) resorcinol, and (5) catechol 相似文献
6.
5,10,15,20-tetrakis(phenoxy acetic acid) porphyrin (PAAP) was covalently linked to Merrifield chloromethylated resin. Characterization
of PAAP and the modified polymeric matrix were performed by 1H NMR, FTIR and elemental analysis. The sorbent was used for the separation and enrichment of the d-electron metals (Mn(II), Co(II), Ni(II), Cu(II) and Zn(II)) at pH 6–8 and of the f-electron metals U(VI) and Th(IV) at pH 4–5. The metals ions were preconcentrated with a concentration factor range of 115–215
and then determined by flame atomic absorption spectrometry or visible spectrophotometry using Arsenazo(III). The retained
metals were eluted with 2.0 mol L−1 HNO3 in the case of the d-electron metals and 0.1/0.25 mol L−1 HCl in the case of the f-electron metals. The procedure was validated by analyzing the NIST standard reference material 2709 (San Joaquin Soil).
Correspondence: Melek Merdivan, Chemistry Department, Faculty of Arts and Sciences, Dokuz Eylul University, 35160 Buca, Izmir,
Turkey 相似文献
7.
Discovery of nitric oxide in marine ecological system and the chemical characteristics of nitric oxide 总被引:1,自引:0,他引:1
ZHANG Zhengbin XING Lei WU Zhenzhen LIU Chunying LIN Cai & LIU Liansheng Institute of Marine Chemistry Ocean University of China Qingdao China 《中国科学B辑(英文版)》2006,49(5):475-480
Nitric oxide was discovered in both the lab and the alga culture pond of Daya Bay (1―300 m3) before the growth of alga reached the maximum. The results included: (1) NO was detected before the growth of alga reached the maximum in the case of red tide alga and food alga, and the concentration of NO decreased rapidly after the growth maximum; (2) the curve between NO con-centration and time indicated that the concentration of NO in the daytime was more than that at night, and the maximal concentration of NO appeared in the midday (1―3 pm); (3) the growth of alga reached the maximum in the alga culture pond of Daya Bay in about 8―10 d, and NO was discovered in 5―7 d; (4) the measured NO concentration was 10-9 mol/L, 10-9―10-8 mol/L, and 10-8 mol/L for Haeterosigma akashiwo, mixed alga in Daya Bay and Chaetoceros Curvisetus individually; (5) the relation of illumination with NO production was discussed. 相似文献
8.
Ewa Gorodkiewicz Paweł Falkowski Anna Sankiewicz Zbigniew Figaszewski 《Central European Journal of Chemistry》2003,1(3):242-259
The analytical properties of an ion-selective electrode sensitive to labetalol with a liquid membrane, based on ion-pair complexes
with sodium tetraphenylborate (TPB-Na+) are described. The studied electrode can be used for the determination of labetalol hydrochloride as a protonated form of
labetalol in pharmaceuticals. The calibration curve, e.g. EMF=f(pC
LabHCl
) is linear in the range from 10−5 to 10−2 mol L−1 with a correlation coefficient of 0.9992 and slope of 61.13 mV/decade, which is close to the Nernstian slope. The detection
limit of the examined electrode is 7.20×10−6 mol L−1. The influence of pH of the tested solutions on the formulation of the electrode is not as considerable since the electrode
works correctly in the pH range 3.0–8.0. The main attributes of the developed electrode are: stability, good reproducibility
of EMF and short response time, close to 30 seconds depending on labetalol concentration in the solution. The electrode shows
good selectivity for many inorganic ions. The selectivity for drug cations is weaker due to the structural similarity of the
interfering cations to labetalol. The results of labetalol determination using direct potentiometry in drugs such as Pressocard
(Polpharma) and Trandate (GlaxoWellcome) were compatible with the quantity of labetalol declared by the manufacturer, and
with parallel UV spectrophotometric and HPLC determinations. 相似文献
9.
Spectrofluorometric determination of hesperidin by manual and flow-injection methods 总被引:1,自引:0,他引:1
T. Pérez-Ruíz C. Martínez-Lozano V. Tomás J. Fenoll 《Fresenius' Journal of Analytical Chemistry》1999,364(3):279-283
A reliable and highly sensitive method for the determination of hesperidin is described. It involves the formation of a highly
fluorescent complex between hesperidin and aluminium (III) in a micellar medium. There is a linear relationship between fluorescence
intensity (λem = 496 nm, λex = 391 nm) and hesperidin concentration over the range 5 × 10–7– 2 × 10–5 mol L–1. The detection limit is 79 μg L–1. The method can easily be adapted to a flow system using a three-channel manifold, the peak height being proportional to
the hesperidin concentration over the range 1 × 10–6– 1 × 10–4 mol L–1. Manual and flow-injection procedures have been successfully applied to the determination of hesperidin in orange peel and
orange juice.
Received: 21 October 1998 / Revised: 16 December 1998 / Accepted: 25 December 1998 相似文献
10.
Dian-Lei Wang Yan Liang Lin Xie Tong Xie X. T. Wang Sen Yu Guang-Ji Wang Xiao-Dong Liu 《Chromatographia》2008,67(3-4):219-224
To evaluate the pharmacokinetics of a novel analogue of ginkgolide B, 10-O-dimethylaminoethylginkgolide B (XQ-1) in rat plasma in pre-clinical studies, a sensitive and specific liquid chromatographic
method with electrospray ionization mass spectrometry detection (LC–ESI–MS) was developed and validated. After a simple extraction
with ethyl acetate, XQ-1 was analyzed on a Shim-pack C18 column with a mobile phase of a mixture of 1 μmol L−1 ammonium acetate containing 0.02% formic acid and methanol (55:45, v/v) at a flowrate of 0.3 mL min−1. Detection was performed in selected ion monitoring (SIM) mode using target ions at [M + H]+
m/z 496.05 for XQ-1 and m/z 432.10 for the internal standard (lafutidine). Linearity was established for the concentration range from 2 to 1,000 ng mL−1 . The extraction recoveries ranged from 86.0 to 89.9% in plasma at concentrations of 5, 50, and 500 ng mL−1. The lower limit of quantification was 2 ng mL−1 with 100 μL plasma. The validated method was successfully applied to a pharmacokinetic study after intragastic administration
of XQ-1 mesylate in rats at a dose of 20 mg kg−1. 相似文献
11.
A rapid and inexpensive method for simultaneous quantification of terbumeton (TER), and its major potential metabolites (TED;
terbumeton-desethyl, TOH; terbumeton-2-hydroxy and TID; terbumeton-deisopropyl) in soil bulk water (SBW) samples is proposed.
The analytical method involves extraction–concentration from SBW samples using a graphitized carbon black (GCB) cartridge
followed by their separation–detection by reversed-phase high-performance liquid chromatography analysis using a C18 column and a diode array detector. A mobile phase of acetonitrile−0.005 mol L−1 phosphate buffer (pH 7.0) (35:65, v/v) at a flow rate of 0.8 mL min−1 in isocratic elution mode has been used. After optimization of the extraction and separation conditions, this method can be
used for the simultaneous determination of investigated compounds in the range of the international limits of 0.1 μg L−1. For TER the detection limit was 0.009 μg L−1 and it was 0.100, 0.550, and 0.480 μg L−1 for TED, TOH, and TID, respectively. The recoveries of TER, TED, TOH, and TID from SBW samples, measured at three levels of
concentration range, were found to be between 48.0 and 102.0%. The intra-day precision measured by relative standard deviation
(RSD) was always lower than 9.0%. 相似文献
12.
Zenovia Moldovan 《Chemical Papers》2009,63(4):385-390
A simple, selective and sensitive kinetic method for the determination of nitrite in water was developed. The method is based
on the catalytic effect of nitrite on the oxidation of methylene blue (MB) with bromate in a sulfuric acid medium. During
the oxidation process, absorbance of the reaction mixture decreases with the increasing time, inversely proportional to the
nitrite concentration. The reaction rate was monitored spectrophotometrically at λ = 666 nm within 30 s of mixing. Linear
calibration graph was obtained in the range of 0.005–0.5 μg mL−1 with a relative standard deviation of 2.09 % for six measurements at 0.5 μg mL−1. The detection limit was found to be 0.0015 μg mL−1. The effect of different factors such as acidity, time, bromate concentration, MB concentration, ionic strength, and order
of reactants additions is reported. Interference of the most common foreign ions was also investigated. The optimum experimental
conditions were: 0.38 mol L−1 H2SO4, 5 × 10.4 mol L−1 KBrO3, 1.25 × 10.5 mol L−1 MB, 0.3 mol L−1 sodium nitrate, and 25°C. The proposed method was conveniently applied for the determination of nitrite in spiked drinking
water samples. 相似文献
13.
Karadjova IB Lampugnani L D'Ulivo A Onor M Tsalev DL 《Analytical and bioanalytical chemistry》2007,388(4):801-807
A rapid, accurate, and precise method is described for the determination of Pb in wine using continuous-flow hydride generation
atomic fluorescence spectrometry (CF-HGAFS). Sample pretreatment consists of ten-fold dilution of wine followed by direct
plumbane generation in the presence of 0.1 mol L−1 HCl and 1% m/v K3[Fe(CN)6] with 1% m/v NaBH4 as reducing agent. An aqueous standard calibration curve is recommended for Pb quantification in wine sample. The method
provides a limit of detection and a limit of quantification of 0.3 μg L−1 and 1 μg L−1, respectively. The relative standard deviation varies between 2–6% (within-run) and 4–11% (between-run) at 3–30 μg L−1 Pb levels in wine. Good agreement has been demonstrated between results obtained by CF-HGAFS and direct electrothermal atomic
absorption spectrometry in analyses of red and white wines within the concentration range of 9.2–25.8 μg L−1 Pb. 相似文献
14.
A method for the determination of total N-acetylcysteine and thioglycolic acid in human urine is described. Because these compounds are mainly excreted as disulfides,
they are first reduced to the free thiols by treatment with tris(2-carboxyethyl)phosphine hydrochloride and then derivatized
with 2-chloro-1-methylquinolinium tetrafluoroborate. Separation and quantitation of the 2-S-quinolinium derivatives of the thiols were achieved by reversed-phase ion-pair liquid chromatography with UV-detection at
355 nm. Because the method enables simultaneous determination of other endogenous urinary thiols, e.g. cysteine and cysteinylglycine,
amounts of these compounds in urine were also studied. Detector responses were linear over the range covering most practical
situations, with correlation coefficients for all four analytes better than 0.999. Recovery and imprecision (as RSD) were
within 99.77–102.17 and 0.01–7.79%, respectively. The lower limit of detection was 0.25 μmol L−1 urine for thioglycolic acid and N-acetylcysteine, and 0.12 μmol L−1 urine for cysteine and cysteinylglycine. The method was used for analysis of urine samples from 29 healthy individuals to
establish reference values for the thiols, normalized to creatinine. 3-Mercaptolactic acid, 2-mercaptopropionic acid, and
mercaptoethanol were not present in the urine analyzed. 相似文献
15.
A fed-batch culture system with constant feeding (glucose 80 g L−1, 0.25 ml min−1) was used to study the influence of glucose on cell dry weight and exopolysaccharides production from submerged Tremella fuciformis spores in a 5-L stirred-tank bioreactor. The results showed that high levels of cell mass (9.80 g L−1) and exopolysaccharides production (3.12 g L−1) in fed-batch fermentation were obtained after 1 h of feeding, where the specific growth rate (μ) and exopolysaccharides yield on substrate consumed (YP/S) were 0.267 d−1 and 0.14 g g−1. Unlike batch fermentation, maximal cell mass and exopolysaccharides production merely reached 7.11 and 2.08 g L−1; the specific growth rate (μ) and exopolysaccharides yield on substrate consumed (YP/S) were 0.194 d−1 and 0.093 g g−1, respectively. It is concluded that the synthesis of exopolysaccharides can be promoted effectively when feeding glucose
at a late exponential phase. 相似文献
16.
Popp M Hann S Mentler A Fuerhacker M Stingeder G Koellensperger G 《Analytical and bioanalytical chemistry》2008,391(2):695-699
A novel method employing high-performance cation chromatography in combination with inductively coupled plasma dynamic reaction
cell mass spectrometry (ICP–DRC–MS) for the simultaneous determination of the herbicide glyphosate (N-phosphonomethylglycine) and its main metabolite aminomethyl phosphonic acid (AMPA) is presented. P was measured as 31P16O+ using oxygen as reaction gas. For monitoring the stringent target value of 0.1 μg L−1 for glyphosate, applicable for drinking and surface water within the EU, a two-step enrichment procedure employing Chelex
100 and AG1-X8 resins was applied prior to HPIC–ICP–MS analysis. The presented approach was validated for surface water, revealing
concentrations of 0.67 μg L−1 glyphosate and 2.8 μg L−1 AMPA in selected Austrian river water samples. Moreover, investigations at three waste water-treatment plants showed that
elimination of the compounds at the present concentration levels was not straightforward. On the contrary, all investigated
plant effluents showed significant amounts of both compounds. Concentration levels ranged from 0.5–2 μg L−1 and 4–14 μg L−1 for glyphosate and AMPA, respectively. 相似文献
17.
Pinheiro AD Rocha MV Macedo GR Gonçalves LR 《Applied biochemistry and biotechnology》2008,148(1-3):227-234
A commercial strain of Saccharomyces cerevisiae was used for the production of ethanol by fermentation of cashew apple juice. Growth kinetics and ethanol productivity were
calculated for batch fermentation with different initial sugar (glucose + fructose) concentrations. Maximal ethanol, cell,
and glycerol concentrations were obtained when 103.1 g L−1 of initial sugar concentration was used. Cell yield (Y
X/S) was calculated as 0.24 (g microorganism)/(g glucose + fructose) using cashew apple juice medium with 41.3 g L−1 of initial sugar concentration. Glucose was exhausted first, followed by fructose. Furthermore, the initial concentration
of sugars did not influence ethanol selectivity. These results indicate that cashew apple juice is a suitable substrate for
yeast growth and ethanol production. 相似文献
18.
L. N. Yang F. Xu L. X. Sun Z. C. Tan H. D. Tan Z. B. Zhao J. G. Liang 《Journal of Thermal Analysis and Calorimetry》2006,85(3):807-810
A microcalorimetric
technique based on the bacterial heat output was applied to evaluate the influence
of antibiotics PIP (Piperacillin Sodium)
and composite preparation of PIP and SBT (Sulbactam
Sodium) on the growth of E. coli
DH5α. The power–time curves of the growth metabolism of E. coli DH5α were studied using a TAM Air Isothermal
Microcalorimeter at 37°C. By analyzing the power–time curves, the
parameters such as growth rate constants (k),
inhibitory ratio (I), the maximum heat
power (P
m) and the
time of the maximum heat power (t
m)
were obtained. The results show that different concentrations of antibiotics
affect the growth metabolism of E. coli
DH5α. The PIP in the concentration range of 0–0.05 μg mL–1
has a stimulatory effect on the E. coli
DH5α growth, while the PIP of higher concentrations (0.05 –0.25
μg mL–1) can inhibit its growth. It seems
that the composite preparation composed of PIP and SBT cannot improve the
inhibitory effect on E. coli DH5α
as compared with the PIP. 相似文献
19.
Yanling Zhao Dan Yan Jiabo Wang Ping Zhang Xiaohe Xiao 《Journal of Thermal Analysis and Calorimetry》2010,102(1):49-55
Using a LKB-2277 bioactivity monitor, stop-flow mode, the power–time curves of Candida albicans growth at 37 °C affected by berberine were measured. The check experiments were studied based on agar cup method to observe
the inhibitory diameter and serial dilution method to determine the minimal inhibitory concentration (MIC) of berberine on
C. albicans growth. By analyzing the quantitative thermogenic parameters taken from the power–time curves using correspondence analysis
(CA), we could find that berberine at a low concentration (5.0 μg mL−1) began to inhibit the growth of C. albicans and at a high concentration (75.0 μg mL−1) completely inhibited C. albicans growth. The anti-fungal activity of berberine could also be expressed as half-inhibitory concentration IC50, i.e., 50% effective in this inhibition. The value of IC50 of berberine on C. albicans was 34.52 μg mL−1. The inhibitory diameters all exceeded 10 mm in test range and the MIC was 500 μg mL−1. Berberine had strong anti-fungal effect on C. albicans growth. This work provided an important idea of the combination of microcalorimetry and CA for the study on anti-fungal effect
of berberine and other compounds. Compared with the agar cup method and serial dilution method, microcalorimetry not only
offered a useful way for evaluating the bioactivity of drugs, but also provides more information about the microbial growth
and all this information was significant for the synthesis and searching of antibiotics. 相似文献
20.
Conde FJ Afonso AM González V Ayala JH 《Analytical and bioanalytical chemistry》2006,385(7):1162-1171
A sampling and analysis method for the determination of 21 phenolic compounds in smoke samples from biomass combustion has
been developed. The smoke is used to make smoked foods, following an artisanal procedure used in some parts of the Canary
Islands. The sampling system consists of a Bravo H air sampler, two impingers, each one containing an aqueous solution of
sodium hydroxide 0.1 mol L−1, followed by a silica gel trap. The variables optimized to reach the best sampling conditions were volume of absorbent solution
and sampling flow. Under the optimum conditions, 100 mL of absorbent solution of NaOH 0.10 mol L−1 and 2 L min−1 for the sampling flow, sampling efficiencies are higher than 80%. Analysis of phenolic compounds was carried out by headspace
solid-phase microextraction (HS-SPME) coupled to gas chromatography–mass spectrometry (GC-MS). Five different fiber coatings
were employed in this study. By means of a central composite design, extraction time, salt concentration, and pH of the solution
were optimized: 65-μm carbowax–divinylbenzene, extraction time 90 min, concentration in NaCl of 35% (m/v), and pH 2 yielded
the highest response. Detection limits of phenol and their alkyl derivatives, guaiacol and eugenol, are between 1.13 and 4.60 ng mL−1. 3-Methoxyphenol, 2,6-dimethoxyphenol, and vanillin have detection limits considerably higher. Good linearity (R
2≥0.98) was observed for all calibration curves in the established ranges. The reproducibility of the method (RSD, relative
standard deviation) was found to oscillate between 7 and 18% (generally close or lower than 10%). 相似文献