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1.
With the use of 32P-labeled phosphate and 42K2CO3 the effect of diphenyl on permeability and uptake properties of the cytoplasmic membrane in wild type and diphenyl-tolerant mutant conidia of Fusarium solani f. cucurbitae was studied. No general damage to the membrane with unspecific leakage of cell constituents was demonstrated under conditions in which diphenyl prevents germination of wild type conidia. The fresh conidia do not require exogenous supply of energy for the uptake of phosphate or of potassium. In the wild type the entry of 32P is inhibited but that of 42K strikingly stimulated by diphenyl. Independently of the tolerant mutant gene present, the mutant conidia are significantly less sensitive to the phosphate uptake inhibition and not affected at all by diphenyl with respect to the uptake of potassium. The latter difference from the wild type seems to indicate genetic control of some property of the potassium transport system in this fungus. 相似文献
2.
Scott A. Martin 《Applied microbiology and biotechnology》1992,37(1):104-108
Summary Glucose uptake by whole cells of Bacteroides ruminicola B14 is constitutive. Potassium concentrations between 10 and 150 mm stimulated uptake over fourfold, while sodium had little effect on uptake. The involvement of potassium in glucose uptake by B. ruminicola was supported by strong inhibition of uptake by the ionophores valinomycin, lasalocid, and monensin. The electron transport inhibitor antimycin A had little effect on uptake, but menadione and acriflavine inhibited uptake by 30 and 48%, respectively. Potent inhibitors of uptake included oxygen, p-chloromercuribenzoate, HgCl2, and o-phenanthroline. Sodium arsenate decreased uptake by 40%, suggesting that a high-energy phosphate compound and possibly a binding protein may be involved in glucose uptake. The protonophores carbonyl cyanide m-chlorophenylhydrazone and 2,4-dinitrophenol inhibited glucose uptake by 37 and 22%, respectively. Little change in uptake activity was observed at extracellular pH values between 4.0 and 8.0. Excess (10 mm) cellobiose, maltose, and sucrose inhibited glucose uptake less than 15%. High levels (0.15% w/v) of p-coumaric acid and vanillin decreased uptake by 32 and 37%, respectively, while 0.15% ferulic acid decreased uptake by 15%. 相似文献
3.
Evidence is presented for low rates of carriermediated uptake of sulphate, thiosulphate and sulphite into the stroma of the C3 plant Spinacia oleracea. Uptake of sulphate in the dark was followed using two techniques (1) uptake of sulphate [35S] as determined by silicon oil centrifugal filtration and (2) uptake as indicated by inhibition of CO2-dependant O2 evolution rates after addition of sulphate.Sulphate, thiosulphate and sulphite were transported across the envelope leading to an accumulation in the chloroplasts. Sulphate transport had saturation kinetics of the Michaelis-Menten type (Vmax : 25 μmoles . mg−1 chl . h−1 at 22°C ; Km : 2.5 mM). The rate of transport for sulphate was not influenced either by illumination or pH change in the external medium. Phosphate was a competitive inhibitor of sulphate uptake by chloroplasts (Ki : 0.7 mM, fig. 1). The rate of transport for phosphate appeared to be much higher than for sulphate. When the chloroplasts were pre-loaded with labelled sulphate, radioactivity was rapidly released after addition of phosphate into the external medium. Consequently, the transport of sulphate occurs by a strict counter-exchange : for each molecule of sulphate entering the chloroplast, one molecule of phosphate leaves the stroma, and vice-versa.The uptake of sulphate by isolated intact chloroplasts exchanging for internal free phosphate induced a lower rate of photophosphorylation, which in turn inhibited CO2-dependent O2 evolution.The presence, on the inner membrane of the chloroplast envelope, of a specific sulphate carrier, distinct from the phosphate translocator, is discussed. 相似文献
4.
The uptake of monovalent cations by yeast via the monovalent cation uptake mechanism is inhibited by phosphate. The inhibition of Rb+ uptake shows saturation kinetics and the phosphate concentration at which halfmaximal inhibition is observed is equal to the Km of phosphate for the sodiumindependent phosphate uptake mechanism. The kinetic coefficients of Rb+ and Tl+ uptake are affected by phosphate: the maximal rate of uptake is decreased and the apparent affinity constants for the translocation sites are increased.In the case of Na+ uptake, the inhibition by phosphate may be partly or completely compensated by stimulation of Na+ uptake via a sodium-phosphate cotransport mechanism.Phosphate effects a transient stimulation of the efflux of the lipophilic cation dibenzyldimenthylammonium from preloaded yeast cells and a transient inhibition of dibenzyldimethylammonium eptake. Possibly, the inhibition of monovalent cation uptake in yeast can be explained by a transient depolarization of the cell membrane by phosphate. 相似文献
5.
Brian E. Peerce 《The Journal of membrane biology》1989,110(2):189-197
Summary The substrate stoichiometry of the intestinal Na+/phosphate cotransporter was examined using two measures of Na+-dependent phosphate uptake: initial rates of uptake with [32P] phosphate and phosphate-induced membrane depolarization using the potential-sensitive dye diSC3(5). Isotopic phosphate measures electrogenic and electroneutral Na+-dependent phosphate uptake, while phosphate-induced membrane depolarization measures electrogenic phosphate uptake. Using these measures of Na-dependent phosphate uptake, three parameters were compared: substrate affinity; phenylglyoxal sensitivity and labeling; and inhibiton by mono- and di-fluorophosphates. Na+/phosphate cotransport was found to have similar Na+ activations (apparentK
0.5's of 28 and 25mm), apparentK
m
's for phosphate (100 and 410 m), andK
0.5's for inhibition by phenylglyoxal (70 and 90 m) using isotopic phosphate, uptake and membrane depolarization, respectively. Only difluorophosphate inhibited Na+-dependent phosphate uptake below 1mm at pH 7.4.Difluorophosphate also protected a 130-kDa polypeptide from FITC-PG labeling in the presence of Na+ with apparentK
0.5 for phosphate of 200 m; similar to the apparentK
m
for phosphate uptake, andK
0.5 for phosphate protection against FITC-PG inhibition of Na+-dependent phosphate uptake and FITC-PG labeling of the 130-kDa polypeptide. These results indicate that the intestinal Na+/phosphate cotransporter is electrogenic at pH 7.4, that H2PO
4
–
is the transport-competent species, and that the 130-kDa polypeptide is an excellent candidate for the intestinal Na+/phosphate cotransporter. 相似文献
6.
D. E. KOEPPE 《Physiologia plantarum》1972,27(1):89-94
The effects of juglone on the uptake of O2 by excised corn roots (Zea mays L., Wf9 cms- T × M14) and isolated corn mitochondria arc reported. The O2 uptake by excised corn roots, as measured by an O2 electrode, was inhibited more than 90% after a one-hour treatment of 500 μM juglone. Lesser inhibitions were observed with 50 μM and 250 μM juglone. In a KC1 reaction medium in the absence of inorganic phosphate (Pi), juglone stimulated the rate of O2 uptake by isolated mitochondria oxidizing NADH, succinate, or malate + pyruvate. In the presence of Pi, juglone concentrations of 3 μM and greater inhibited the state 3 oxidation rates of succinate and malate + pyruvate, lowered respiratory control and ADP/O ratios obtained from the oxidation of NADH, malate + pyruvate, or succinate, and reduced the coupled deposition of calcium phosphate within isolated mitochondria driven, by the oxidation of malate + pyruvate. The inhibition of state 3 O2 uptake by isolated mitochondria, an oxidative state in which electron transfer is coupled to ATP production, is seen to correlate with the inhibition affected by juglone when applied to tissues in vivo. 相似文献
7.
Summary The effects of p, p-DDT were determined on photosynthesis and chlorophyll a content in the marine diatom Nitzschia delicatissima Cleve at four light intensities. A consistent reduction in carbon fixation and chlorophyll a per cell over controls in a 24-hour period was observed with increasing DDT concentration between 9.4 ppb and 1000 ppb. The maximum reductions of carbon uptake, chlorophyll a and carbon/chlorophyll a uptake per cell occurred at the highest light intensities. Carbon fixation per cell was reduced by as much as 94% in water containing an initial DDT concentration of 100 ppb, and chlorophyll a per cell by as much as 86% in 220 ppb DDT. Above 100 ppb, further decreases of carbon fixation and chlorophyll a per cell were not observed. Distortion of the chloroplasts in the cells exposed to DDT was also observed at the lowest concentration of DDT used. At 1000 ppb, chloroplasts were totally destroyed within 24 hours.
Zusammenfassung Die Wirkung von p, p-DDT auf Photosynthese und Chlorophyll a Gehalt der Meeresdiatomee Nitschia delicatissima Cleve wurde untersucht unter vier Lichtintensitäten. Bei DDT Konzentrationen, steigend von 9,4 ppb bis 1000 ppb, wurde eine fortschreitende Reduktion der Kohlenstoff bindung und des Chlorophyll a Gehaltes pro Zelle gefunden, wobei die höchtse Lichtintensität die stärkste Reduktion, sowie auch die niedrigste Kohlenstoff/Chlorophyll a Aufnahme pro Zelle zeigte. In Wasser mit anfänglichem DDT Gehalt von 100 ppb, wurde die Kohlenstoff bindung pro Zelle 94% reduziert und beim DDT Gehalt von 220 ppb, wurde der Chlorophyll a Gehalt mit 86% reduziert. Bei Konzentrationen über 100 ppb, fielen Kohlenstoff bindung und Chlorophyll a Gehalt pro Zelle nicht weiter ab.Schädigungen der Chloroplasten in der Zelle wurden schon bei den niedrigsten DDT Gehalten festgestelt. Bei 100 ppb wurden die Chloroplasten innerhalb 24 Stunden völlig zerstört.相似文献
8.
The characteristics of phosphate uptake in synchronized populations of Euglena gracilis Klebs (Z) were studied. The cells were grown autotrophically in batch culture and synchronized with a cycle of 14:10 LD. Incorporation of P was nonlinear with time for the first 2 h of incubation over a wide range of P concentrations and completely inhibited by darkness. The kinetics of P uptake as a function of P concentration were triphasic between 0 and 100 μM PO4, obeying Michaelis-Menten kinetics over the 0–3 μM PO4 range-only. Uptake velocity increased linearly with, concentration above 3 μM PO4. The kinetics of P uptake varied with stage in the cell cycle. The half-saturation constant for uptake at the lower concentrations oscillated between 0.7 and 2.8 μM PO4, reaching a peak immediately before the onset of cell division (beginning of the dark period). Vmax was largest in the middle of the light period, as was the slope of the linear portion of the kinetic pattern. Further analysis of the kinetics suggests that changes in this slope are responsible for the oscillation in Ks values calculated for the lower concentrations. This analysis assumes 2 uptake mechanisms, one which saturates at low concentrations of phosphate, and one which is nonsaturable over the entire concentration range examined. 相似文献
9.
The metabolites produced by Stigmatella WXNXJ-B inhibited the growth of tumor cells. The aims of this research were to evaluate the inhibition potency to different
tumor cell lines and to study the effects of ammonium, phosphate and iron salts on bacterial growth and production of bioactive
metabolites in Stigmatella WXNXJ-B fermentation. The results showed that the chloroform extract (CE-ME) showed the strongest growth inhibition bioactivity
on mouse melanoma cell line (B16), murine colon carcinoma cell line (CT-26), human liver carcinoma cell line (HepG2) and human
breast cancer cell line (MDA-MB231) in vitro and the IC50 values were 9.94, 7.33, 11.34 and 11.66 μg ml−1 respectively. The IC50 value was above 700 μg ml−1 on normal mouse spleen cells. Morphology happened changes in B16 cells treated with CE-ME. The anti-tumor metabolites were
mainly produced during the stationary phase of the bacterial growth. Cell growth was stimulated at the phosphate concentration
below 5 mM, but it was inhibited partly with 10 mM phosphate. The production of bioactive substances was inhibited by the
phosphate. Ammonium increased the cell growth by 250% at 5 mM addition. The inhibition rate to B16 cells was increased to
89% at the concentration of 40 mM ammonium. The bacteria showed the best growth with 4 mM iron. Iron had little effect on
the production at 2 mM, but bigger inhibition effect at higher iron concentration. 相似文献
10.
The cells used in the present investigation had a phosphate content of about 20 per cent as compared with the status in normal cultures. The uptake of phosphate during a period of 4 hours was determined at a pH of 6,5, kept constant with the aid of a citrate buffer. In the absence of CO2, light increased the uptake of phosphate with saturation around 14,000 erg/cm2s. With 5 per cent CO2 in the air the relationship was more complicated, and the uptake of phosphate must he related to more than one process during active photosynthesis. The inhibiting effect of CO2 in air was noticeable already at low concentrations both in light and in darkness. With the system used, this supports earlier indications for internal recycling of orthophosphate, CO2 was inhibiting also in nitrogen in the light. Selenate in a concentration of 2 mM gave a slight and rather irregular inhibition.—Anaerobiosis had no effect in the light but gave a large decrease in the dark.—DNP (0.1 mM) was somewhat more active in the dark than in the light. The lower concentrations tested had no effect in either case.—Menadione (0.1 mM) inhibited strongly, and more in illuminated than in non-illuminated cells. 相似文献
11.
José de JesÚs Garcia M. Tuena de Gómez-Puyou A. Gómez-Puyou 《Journal of bioenergetics and biomembranes》1995,27(1):127-136
The effect of trifluoperazine (TFP) on the ATPase activity of soluble and paniculate F1ATPase and on ATP synthesis driven by succinate oxidation in submitochondrial particles from bovine heart was studied at pH 7.4 and 8.8. At the two pH. TFP inhibited ATP hydrolysis. Inorganic phosphate protected against the inhibiting action of TFP. The results on the effect of various concentrations of phosphate in the reversal of the action of TFP on hydrolysis at pH 7.4 and 8.8 showed that H2PO
4
–
is the species that competes with TFP. The effect of TFP on oxidative phosphorylation was studied at concentrations that do not produce uncoupling or affect the aerobic oxidation of succinate (<15M). TFP inhibited oxidative phosphorylation to a higher extent at pH 8.8 than at pH 7.4; this was through a diminution in theV
max, and an increase in theK
m for phosphate. Data on phosphate uptake during oxidative phosphorylation at several pH showed that H2PO
4
–
is the true substrate for oxidative phosphorylation. Thus, in both synthesis and hydrolysis of ATP, TFP and H2PO
4
–
interact with a common site. However, there is a difference in the sensitivity to TFP of ATP synthesis and hydrolysis; this is more noticeable at pH 8.8, i.e. ATPase activity of soluble F1 remains at about 40% of the activity of the control in a concentration range of TFP of 40–100M, whereas in oxidative phosphorylation 14M TFP produces a 60% inhibition of phosphate uptake. 相似文献
12.
Regulation of phosphate uptake kinetics inOscillatoria agardhii 总被引:1,自引:0,他引:1
In order to study phosphate uptake kinetics the cyanobacteriumOscillatoria agardhii was grown in continuous culture under a phosphorus limitation. The affinity of the uptake system reflected in the initial slope of the uptake rate versus external substrate concentration curve (dV/ds) was found to be unaffected by the growth wate.The maximum phosphate uptake rate (V
m
) decreased as the growth rate was increased. Attempts were made to relate the decrease ofV
m
to the increase in phosphorus content of the cells that occurred a higher growth rates. Accumulation of phosphate during pulse experiments indeed resulted in a decrease ofV
m
. However feedback regulation ofV
m
by accumulated phosphorus was found to occur only to a small extent in steady state growing cells. The main part of the regulation of the activity of the phosphate uptake system seemingly is determined by a long term process that is, at least longer than 2 h. The presence of short term feedback inhibition by accumulated phosphorus on the activity of the uptake system provides an explanation of the phenomenon thatOscillatoria agardhii is not able to grow at near
max growth rates under a phosphorus limitation. 相似文献
13.
Cations, including calcium, magnesium, potassium, sodium, copper, iron, nickel and zinc, inhibited (up to 40%) extracellular binding and intracellular uptake of cadmium by Lemna polyrhiza in solution culture. Test plants showed a high capacity of extracellular cadmium binding which was competitively inhibited by copper, nickel and zinc; however, calcium, magnesium and potassium caused non-competitive inhibition. Iron and sodium increased K
m and decreased V
max, thereby causing mixed inhibition of extracellular binding. Intracellular cadmium uptake displayed Michaelis-Menten kinetics. It was competitively inhibited by calcium, magnesium, iron, nickel and zinc. Monovalent cations (sodium and potassium) caused non-competitive and copper caused mixed inhibition of intracellular cadmium uptake. Thus, high levels of cations and metals in the external environment should be expected to lower the cadmium accumulation efficiency of L. polyrhiza. 相似文献
14.
Abstract Proton extrusion of maize root Zea mays segments, was inhibited by the presence of Cr (o.n. + 6; present in solution as CrO42-, Cr2O72-) in the incubation medium: the minimum inhibiting concentration was 2 × 10?3 mol m?3 and the inhibition progressively increased with Cr concentration. Cr inhibited proton extrusion. Also, when this activity was stimulated by the presence of K+ or fusicoccin (FC) in the incubation medium, the K+ and FC stimulating effect was still present when proton extrusion was inhibited by Cr. In addition, Cr inhibited K+ uptake. This inhibition was higher (50%) at K+ concentrations up to 1 mol m?3 lower (15%) at higher K+ concentrations. This result indicates that the system responsible for K+ uptake operating at low K+ concentrations is more sensitive to Cr inhibition. Cr had no effect on transmembrane electric potential (PD). The depolarizing and hyper-polarizing effect of K+ and FC, respectively, were not affected by Cr; but Cr enhances the depolarizing effect of the uncoupler carbonylcyanide m-chlorophenylhydrazone (CCP). These results indicate that Cr inhibited the proton translocating mechanism coupled with K+ uptake, but did not change the net transport of charges through the plasmalemma. The Cr effect is discussed, taking into account the possibility of a direct effect of Cr at the membrane level or, alternatively, of an effect on some metabolic processes controlling membrane function. 相似文献
15.
A. Kotyk 《The Journal of membrane biology》1994,138(1):29-35
Acidification of the external medium of the yeast Saccharomyces cerevisiae, mainly caused by proton extrusion by plasma membrane H+-ATPase, was inhibited to different degrees by D2O, diethylstilbestrol, suloctidil, vanadate, erythrosin B, cupric sulfate and dicyclohexylcarbodiimide. The same pattern of inhibition was found with the uptake of amino acids, adenine, uracil, and phosphate and sulfate anions. An increase of the acidification rate by dioctanoylglycerol also increased the rates of uptake of adenine and of glutamic acid. In contrast, a decrease of the membrane potential at pH 4.5 from a mean of -40 to -20 mV caused by 20 mm KC1 had no effect on the transport rates. The ATPase-deficient mutant S. cerevisiae pmal-105 showed a markedly lower uptake of all the above solutes as compared with the wild type, while its membrane potential and pH were unchanged.Other types of acidification (spontaneous upon suspension; K+ stimulated) did not affect the secondary uptake systems. 相似文献
16.
We found that species-specific differences exist among a variety of freshwater algae and cyanobacteria in the extent to which growth and photosynthesis are inhibited by vanadium. A major factor controlling the degree of inhibition by vanadium was the phosphorus state (P-sufficient vs. P-deficient) of the organisms. In P-sufficient cultures, vanadium was inhibitory when the vanadium concentration exceeded the phosphate concentration. In P-deficient cultures, the depression of photosynthesis by vanadium increased with increasing phosphorus deficiency. Our conclusion that vanadium competed with phosphate for uptake sites was supported by the following three observations: 1) the decreased influx of 32P-PO 4 into P-deficient cells in the presence of vanadium, 2) the amelioration of vanadium inhibition of photosynthesis by the addition of phosphate, and 3) the accumulation of vanadium by cells. At vanadium concentrations that severely inhibited growth, the cells of Scenedesmus obliquus (Turp.) Kruger were larger than normal and contained more vacuoles, lipid, and starch bodies than normal cells. Four-celled coenobia were replaced by unicells. Scenedesmus acutusf: alternans Hortobagyi cells from vanadium-inhibited cultures had 7.5 times more vanadium per cell than control cultures and contained numerous granules that did not stain for polyphosphate and may be composed of condensed vanadate molecules. The cellular P quota and turnover time of PO4in the medium are important regulators of the extent of inhibition by vanadium. 相似文献
17.
ROLF A. OLSEN 《Physiologia plantarum》1971,25(3):503-508
A venacin, the resistance factor in oat roots against Ophiobolus graminis var. graminis, and a related triterpeneglycoside, aescin, inhibited the uptake of K+ and Mg2+ in the fungal mycelium both in phosphate and succinate buffers. The uptake of the cations in Neurospora crassa was similarly inhibited when the inhibitors were dissolved in phosphate or acetatebuffer, while no decrease in the uptake of K+ and Mg2+ was observed when the inhibitors were dissolved in succinate buffer. The uptake of cations in Aspergillus niger and Pythium irregulare was more or less unaffected by aescin. The uptake of inorganic phosphate was in no case inhibited, but some decrease of the accumulation of inorganic phosphate in Ophiobolus graminis and Ncurospora crassa due to inhibitor treatment in phosphate buffer was observed. No accumulation of Ca2+ was observed in any of the tested fungi. 相似文献
18.
Charles L. Meyer Joseph W. Roos Eleftherios T. Papoutsakis 《Applied microbiology and biotechnology》1986,24(2):159-167
Summary When continuous, steady-state, glucose-limited cultures ofClostridium acetobutylicum were sparged with CO, the completely or almost completely acidogenic fermentations became solventogenic. Alcohol (butanol and ethanol) and lactate production at very high specific production rates were initiated and sustained without acetone, and little or no acetate and butyrate formation. In one fermentation, strong butyrate uptake without acetone formation was observed. Growth could be sustained even with 100% inhibition of H2 formation. Although CO gasing inhibited growth up to 50%, and H2 formation up to 100%, it enhanced the rate of glucose uptake up to 300%. TheY
ATP was strongly affected and mostly reduced with respect to its steady-state value. The results support the hypothesis that solvent formation is triggered by an altered electron flow. 相似文献
19.
Because photosynthetic rates in C4 plants are the same at normal levels of O2 (c, 20 kPa) and at c, 2 kPa O2 (a conventional test for evaluating photorespiration in C3 plants) it has been thought that C4 photosynthesis is O2 insensitive. However, we have found a dual effect of O2 on the net rate of CO2 assimilation among species representing all three C4 subtypes from both monocots and dicots. The optimum O2 partial pressure for C4 photosynthesis at 30 °C, atmospheric CO2 level, and half full sunlight (1000 μmol quanta m?2 s?1) was about 5–10 kPa. Photosynthesis was inhibited by O2 below or above the optimum partial pressure. Decreasing CO2 levels from ambient levels (32.6 Pa) to 9.3 Pa caused a substantial increase in the degree of inhibition of photosynthesis by supra-optimum levels of O2 and a large decrease in the ratio of quantum yield of CO2 fixation/quantum yield of photosystem II (PSII) measured by chlorophyll a fluorescence. Photosystem II activity, measured from chlorophyll a fluorescence analysis, was not inhibited at levels of O2 that were above the optimum for CO2 assimilation, which is consistent with a compensating, alternative electron How as net CO2 assimilation is inhibited. At suboptimum levels of O2, however, the inhibition of photosynthesis was paralleled by an inhibition of PSII quantum yield, increased state of reduction of quinone A, and decreased efficiency of open PSII centres. These results with different C4 types suggest that inhibition of net CO2 assimilation with increasing O2 partial pressure above the optimum is associated with photorespiration, and that inhibition below the optimum O2 may be caused by a reduced supply of ATP to the C4 cycle as a result of inhibition of its production photochemically. 相似文献
20.
Thomas Jahns 《Archives of microbiology》1994,161(3):207-214
The uptake of glutamine was studied in Bacillus pasteurii DSM 33. Only one uptake system was detected in the concentration range studied (between 1 and 100 M glutamine) which exhibited Michaelis-Menten saturation kinetics, with an apparent K
t of 10.7 (±3.5) M glutamine. The uptake was sodium-dependent (apparent K
t=0.2 mM Na+); none of several monovalent cations tested was able to replace sodium in the uptake reaction. Ionophores interfering with proton, sodium or potassium gradients across membranes strongly inhibited uptake of glutamine. Low uptake rates correlating with low potassium content and an acidic cytoplasm were measured in cells grown at high ammonium1 concentrations. Ammonium and other permeant amines as well as potassium stimulated the uptake reaction in these cells, leading to an increase of up to 100-fold in V
max without affecting the affinity of the uptake system. In cells grown at low concentrations of ammonium, an alkaline cytoplasm and both high glutamine uptake activities and potassium content were measured; the uptake reaction was not further stimulated by permeant amines or potassium in such cells. Growth of the strain was inhibited by Tris at high concentrations; this inhibition was relieved by the addition of increasing amounts of ammonium.Abbreviations CCCP
carbonylcyanide-m-chlorphenylhydrazone
- DCCD
dicyclohexylcarbodiimide
This work is dedicated to Prof. Dr. H. Kaltwasser on the occasion of his 60th birthday 相似文献