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1.
Amplification of phleomycin induced death and DNA breakdown by caffeine in Escherichia coli 总被引:2,自引:0,他引:2
G. W. Grigg 《Molecular & general genetics : MGG》1970,107(2):162-172
Summary Caffeine enhanced the degradation of DNA to acid soluble fragments in cultures of Escherichia coli exposed to Phleomycin (2 g/ml). Enhancement was particularly striking with stationary phase cultures, which normally exhibit negligible DNA breakdown when treated with 2 g/ml of Phleomycin. There is little DNA breakdown or death in UVR strains treated with phleomycin (2 g/ml) during exponential growth but when caffeine was present as well as Phleomycin, the kinetics of DNA breakdown and the amounts of DNA degraded were identical in all cultures tested including those of UVR, EXR, B/r type and B strains and equal to the maximum rate observed (with an EXR strain) in the absence of caffeine (ca. 1.7 % per min). High concentrations of Phleomycin (10 g/ml) had the same effect as the caffeine+Phleomycin (2 g/ml) combination and produced a uniform pattern of DNA breakdown in all strains tested. Caffeine did not seem to increase permeability of the bacterial coat. Given to the cells before exposure to Phleomycin it was ineffective in enhancing DNA breakdown. On the other hand, exposure of the bacteria to Phleomycin for a period of 40 min at 37° followed by caffeine was as effective as adding the two drugs together.Caffeine increased the efficiency of Phleomycin as an antibiotic for both growing and stationary phase cultures of e. coli B. It is suggested that caffeine aids the cooperative denaturation of DNA initiated by the attachment of Phleomycin molecules to thymine bases. This would allow single strand-specific endonucleases to attack the DNA and initiate DNA breakdown and cell death.This paper is dedicated to charlotte Auerbach on the occasion of her official retirement. 相似文献
2.
M. Hühn 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1985,70(4):383-389
Summary Theoretical studies on the optimal numbers of components in mixtures (for example multiclonal varieties or mixtures of lines) have been performed according to phenotypic yield stability (measured by the parameter variance). For each component i, i = 1, 2,..., n, a parameter ui with 0 ui 1 has been introduced reflecting the different survival and yielding ability of the components. For the stochastic analysis the mean of each ui is denoted by u
1 and its variance by
i
2
For the character total yield the phenotypic variance V can be explicitly expressed dependent on 1) the number n of components in the mixture, 2) the mean
of the
i
2
3) the variance of the
i
2
4) the ratio
and 5) the ratio
i
2
/2 where denotes the mean of the u
i and
u
2
is the variance of the u
j. According to the dependence of the phenotypic stability on these factors some conclusions can be easily derived from this V-formula. Furthermore, two different approaches for a calculation of necessary or optimal numbers of components using the phenotypic variance V are discussed: A. Determination of optimal numbers in the sense that a continued increase of the number of components brings about no further significant effect according to stability. B. A reduction of b % of the number of components but nevertheless an unchanged stability can be realized by an increase of the mean of the u
i by 1% (with
and
u
2
assumed to be unchanged). Numerical results on n (from A) and 1 (from B) are given. Computing the coefficient of variation v for the character total yield and solving for the number n of components one obtains an explicit expression for n dependent on v and the factors 2.-5. mentioned above. In the special case of equal variances,
i
2
=
o
2
for each i, the number n depends on v, x = (0/)2 and y = (u/)2. Detailed numerical results for n = n (v, x, y) are given. For x 1 and y 1 one obtains n = 9, 20 and 79 for v = 0.30, 0.20 and 0.10, respectively while for x 1 and arbitrary y-values the results are n = 11, 24 and 95.This publication is an extended version of a lecture given at the 1984-EUCARPIA meeting (Section Biometrics in Plant Breeding) in Stuttgart-Hohenheim (Federal Republic of Germany) 相似文献
3.
David H. Foster 《Biological cybernetics》1972,11(4):223-229
An experiment is described which shows in operation the program set out in Foster (1972a) for the investigation of the invariance transformations of visual recognition. The concern in the present study is with the Lie group of rotations SO(2), and a certain centrally located foveal Landolt ring. By presenting to the visual system this Landolt ring and a rotated image in rapid succession, one attempted to induce a specified rotation-type phi-motion. Two subjects were employed. Both reported the existence of the required type of phi-motion for rotations 0 of the Landolt ring about the visual axis with -2/72/7. By appealing to the basic Proposition 2 of Foster (1972 a), the conclusion is reached that the visual system appears capable of effecting upon a certain centrally located foveal annulus the local 1-parameter group of rotations about the visual axis 0, [–2/7,2/7]. 相似文献
4.
Yoshiharu Matahira Atsushi Tashiro Toshinari Sato Hirokazu Kawagishi Taichi Usui 《Glycoconjugate journal》1995,12(5):664-671
N-acetylhexosaminidase fromNocardia orientalis catalysed the synthesis of lacto-N-triose II glycoside (-d-GlcNAc-(1-3)--d-Gal-(1-4)--d-Glc-OMe,3) with its isomers -d-GlcNAc-(1-6)--d-Gal-(1-4)--d-Glc-OMe (4) and -d-Gal-(1-4)-[-d-GlcNAc-(1-6)]--d-Glc-OMe (5) throughN-acetylglucosaminyl transfer fromN,N-diacetylchitobiose (GlcNAc2) to methyl -lactoside. The enzyme formed the mixture of trisac-charides3, 4 and5 in 17% overall yield based on GlcNAc2, in a ratio of 20:21:59. Withp-nitrophenyl -lactoside as an acceptor, the enzyme also producedp-nitrophenyl -lacto-N-trioside II (-d-GlcNAc-(1-3)--d-Gal-(1-4)--d-Glc-OC6H4NO2-p,6) with its isomers -d-GlcNAc-(1-6)--d-Gal-(1-4)--d-Glc-OC6H4NO2-p (7) and -d-Gal-(1-4)-[-d-GlcNAc-(1-6)]--d-Glc-OC6H4NO2-p (8). In this case, when an inclusion complex ofp-nitrophenyl lactoside acceptor with -cyclodextrin was used, the regioselectivity of glycosidase-catalysed formation of trisaccharide glycoside was substantially changed. It resulted not only in a significant increase of the overall yield of transfer products, but also in the proportion of the desired compound6.Abbreviations GlcNAc2
2-acetamido-2-deoxy--d-glucopyranosyl-(1-4)-2-acetamido-2-deoxy-d-glucose
- NAHase
N-acetylhexosaminidase
- -CD
-cyclodextrin 相似文献
5.
The presence of active mitochondria and oxidative metabolism is shown to be essential to maintain low inhibition levels by ethanol of the growth rate (), fermentation rate (v) or respiration rate () of Saccharomyces cerevisiae wild type strain S288C. Cells which have respiratory metabolism show K
i (ethanol inhibition constant) values for , v and , higher (K
i>1 M) than those of petite mutants or grande strains grown in anaerobiosis (K
i=0.7 M). In addition, the relationship between or v and ethanol concentration is linear in cells with respiratory metabolism and exponential in cells lacking respiration. When functional mitochondria are transferred to petite mutants, the resulting strain shows K
i values similar to those of the grande strain and the inhibition of and v by increasing ethanol concentrations becomes linear. 相似文献
6.
A. Reißland 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1978,123(1):71-84
Summary Trichobothria of the house spidersTegenaria atrica (C.L. Koch) andTegenaria derhami (Scopoli) were stimulated by linear deflection of the hair from its resting position to one side. The pulse response of the receptor cell was analyzed. At angular deflection velocities of 10–21 deg/ms the receptor begins to discharge at an angle of 3 degrees. While the mean pulse rate remains constant during deflections of 10–210–1deg/ms the pulse train may be interrupted by repeated breaks. Discharge continues when the hair is bent proximally beyond the bothrium edge. When the hair is bent distally and touches the bothrium edge, however, discharge ceases. Responsible for this phenomenon seems to be an asymmetry of hair suspension. — Repeated deflection leads to logarithmically ascending latency curves and logarithmically falling curves of the pulse numbers. The function coefficients depend on velocities and repetition rates of the deflections. The adaptational effect is heightened by preceding stationary deflection in the direction of the dynamical stimulus. The mean pulse rate as a function of hair deflection velocity increases logarithmically. The mean pulse rate as a function of hair movement direction obeys a cosine law, provided that a given velocity and a definite deflection angle are used.Supported by grants of the Deutsche Forschungsgemeinschaft given to Prof. Dr. P. Görner in the field of the Schwerpunktprogramm RezeptorphysiologieThe present paper is part of a doctoral thesis. My thanks are due to Prof. Dr. P. G6rner for the theme, many valuable discussions and his constant readiness to help. 相似文献
7.
Donat-P. Häder 《Archives of microbiology》1984,140(1):34-39
UV-B irradiation has a detrimental effect on the survival of populations of the filamentous cyanobacterium, Phormidium uncinatum, at levels slightly higher than those currently measured at the surface of the earth. The organisms are not damaged or killed by UV-B radiation at 300 nm of 200 Wm-2 for up to 20 h; but slightly increased levels of UV-B irradiation (2 h of 200 Wm-2 at 300 nm) drastically impair motility, phototactic orientation and photophobic responses. These photosynthetic organisms require a narrow light intensity range for growth so that any decrease in their ability to actively search for and move into areas of favorable light conditions is bound to affect the survival of a population. The fluorescence yield of both phycobilins and chlorophyll is not altered even after 20 h of UV-B irradiation (200 Wm-2 at 270 nm) indicating that UV-B at that dose does not affect the photosynthetic apparatus. The organisms are killed either by too bright intensities which bleach the photosynthetic pigments or by the lack of energy when they are unable to avoid moving into dark areas. 相似文献
8.
Control of yeast fed-batch process through regulation of extracellular ethanol concentration 总被引:3,自引:3,他引:0
At high growth rates, the biomass yield of bakers yeast (Saccharomyces cerevisiae) decreases due to the production of ethanol. For this reason, it is standard industrial practice to use a fed-batch process whereby the specific growth rate, , is fixed at a level below the point of ethanol production, i.e., crit. Optimally, growth should be maintained at crit, but in practice, this is difficult because crit is dependent upon strain and culture conditions. In this work, growth was maintained at a point just above crit by regulating ethanol concentration in the bioreactor. The models used for control design are shown, as are the experimental results obtained when this strategy was implemented. This technique should be applicable to all microorganisms that exhibit an overflow type metabolism. 相似文献
9.
Antonio Moretti Glenn A. Bennett Antonio Logrieco Antonio Bottalico Marian N. Beremand 《Mycopathologia》1995,131(1):25-29
Forty-three strains ofFusarium moniliforme isolated from infected maize and sorghum plants in Italy were assayed for their ability to produce fertile crosses with A and F mating population tester strains, in relation to their ability to produce fumonisins on maize substrate. Most of the strains isolated from maize (ear and stalk rot and maize-based feed), producing fumonisin B1 (FB1) and B2 (FB2) (up to 4,100 and 855 mg/kg, respectively), belonged to the A mating population. All of the strains isolated from sorghum belonged to the F mating population and produced little or no FB1 and FB2. This is the first report of the occurrence of mating population F in Europe. Our data on strains from Italy are consistent with previous studies from the United States that found significant differences in sexual fertility and fumonisin production between strains from maize and sorghum. 相似文献
10.
Sarah Ehrlich-Rogozinski Antonio De Maio Halina Lis Nathan Sharon 《Glycoconjugate journal》1987,4(4):379-390
The interaction of125I-labeledErythrina cristagalli agglutinin (ECA) with neutral glycosphingolipids on thin layer chromatograms was examined by the overlay technique followed by radioautography. The lectin bound topara-globoside with a sensitivity about 10 times higher than to lactosylceramide or globoside, in agreement with the specificity of the lectin forN-acetyllactosamine. The lower limit of detection ofpara-globoside was about 0.66 nmol. The specific binding of ECA to this glycolipid was confirmed by a highly sensitive enzyme-linked lectin assay (ELLA), utilizing the horseradish peroxidase-avidin-biotin system for detection of bound lectin. Overlays of neutral glycosphingolipid extracts from human erythrocyte membranes and from human granulocytes with ECA demonstrated that the lectin can be employed for the detection of small amounts ofpara-globoside in biological materials also in the presence of excess globoside. No staining was obtained when thin layer chromatograms of neutral glycosphingolipid extracts from rabbit erythrocyte membranes were overlayed with125I-ECA. Afterin situ treatment of the chromatograms with -galactosidase, the lectin bound to several components, one of which had a mobility corresponding to that of the pentahexosylceramide Gal3Gal4GlcNAc3Gal4Glc1Cer, the major neutral glycosphingolipid of rabbit erythrocytes, thus providing further evidence for the specificity of ECA forpara-globoside.Abbreviations GSL
glycosphingolipid(s)
- CDH
lactosylceramide, Gal4Glc1Cer
- CTH
trihexosylceramide, Gal4Gal4Glc1Cer
- GLOB
globoside, GalNac3Gal4Gal4Glc1Cer
- PG
para-globoside, Gal4GlcNAc3Gal4Glc1Cer
- AsGM1
asialo-GM1, Gal3GalNAc4Gal4Glc1Cer
- FORS
Forsmann antigen, GalNAc3GalNAc3Gal4Gal4Glc1Cer
- CPH
pentahexosylceramide, Gal3Gal4GlcNAc3Gal4Glc1Cer
- ECA
Erythrina cristagalli agglutinin
- SBA
soybean agglutinin
- PBS
phosphate-buffered saline
- PVP-40
polyvinylpyrrolidone M.W. 40000
- BSA
bovine serum albumin
- HRP-avidin
horseradish peroxidase conjugated to avidin
- ELLA
enzyme-linked lectin assay
- ELISA
enzyme-linked immunosorbent assay
- PMNL
polymorphonuclear leukocytes
- HPTLC
high performance thin layer chromatography 相似文献
11.
Structures of mitochondrial bc
1 complex have been reported based on four different crystalforms by three different groups. In these structures, the extrinsic domain of the Rieske [2Fe–2S]protein, surprisingly, appeared at three different positions: the c
1 position, where the [2Fe–2S]cluster exists in close proximity to the heme c
1; the b position, where the [2Fe–2S] clusterexist in close proximity to the cytochrome b; and the intermediate position where the[2Fe–2S] cluster exists in between c
1 and b positions. The conformational changes betweenthese three positions can be explained by a combination of two rotations; (1) a rotation of theentire extrinsic domain and (2) a relative rotation between the cluster-binding fold and thebase fold within the extrinsic domain. The hydroquinone oxidation and the electron bifurcationmechanism at the QP binding pocket of the bc
1 complex is well explained using theseconformational changes of the Rieske [2Fe–2S] protein. 相似文献
12.
D. Lerche 《The Journal of membrane biology》1976,27(1):193-205
Summary By means of a laser-interferometrical method diffusion layers at the interface of a noncharged cellulose membrane are studied. These layers are induced by a concentration difference between the NaCl solutions separated by the membrane. The temporal and local shift of the NaCl concentration in the diffusion layers were measured. A steady-state concentration profile could be obtained for times of 121 sect
0484 sec. The concentration profiles at any time (t
0900) are not a linear function of the membrane surface, but could be fitted to a quadratic function. The thickness of the diffusion layers is also a function of time and its stationary value in this system is (575±49)×10–6 m. The role of concentration polarization for the determination of phenomenological thermodynamic coefficients of membranes is discussed and a new method is suggested, which excludes the difficulties of the concentration polarization in the diffusion layers at the membrane. 相似文献
13.
Summary We have used two different methods to study the rates of RNA polymerase subunit synthesis in haploid Escherichia coli K12, and a KLF10 rpoB,C
+ merodiploid derivative, when grown in glucose-minimal medium at 37°C. Our results indicate that the haploid strain produces , , and in the molar ratios, 1.01:0.99:2.90:0.26; and that all these subunits are reasonably stable during subsequent growth. The merodiploid produces at the same rate as the haploid, and at a 42% higher rate, and sigma at twice the rate. Some 40% of the newly synthesised and is degraded within one hour; the residuum is as stable as in the haploid. is stable throughout. By contrast, sigma is subject to a marked and continuous turnover in the merodiploid. These results are discussed in terms of gene dosage and regulatory effects. 相似文献
14.
Jacques Raymond Brahim Mimouni Jean-Louis Azanza 《Plant Systematics and Evolution》1994,193(1-4):69-79
The seed storage globulins from sixHelianthus and four hybrids were studied using mono and bidimensional gel SDS electrophoresis (+ 2 mercaptoethanol). The polypeptide composition of each subunit was determined. Different pairs are specifically expressed according to the species studied. Three typical patterns were discriminated. All the studied species exhibit five subunits: two of them are expressed in all the species (11 and 22). The subunit corresponding to the 11 pair is present inH. petiolaris and in the three populations ofH. annuus studied. The 2b2 pair is common toH. annuus andH. argophyllus. H. petiolaris presents two specific 2a2 and 44 pairs andH. annuus a specific 33 pair. InH. argophyllus 11 33 or 44 are never observed but are replaced by 13 and 31 pairs. Some globulins, poorly represented, are of forms but present chains of higher molecular weights (in the range 54–56 kDa). Expressing variations in the banding patterns between these species by the use of a similarity index reveals complete identity between the three populations ofH. annuus. Identity between the twoH. petiolaris studied is also observed.H. annuus andH. argophyllus appear to be closer to each other thanH. petiolaris concerning the seed storage globulins. 相似文献
15.
Gabor L. Igloi Andreas Meinke István D?ry Hans K?ssel 《Molecular & general genetics : MGG》1990,221(3):379-394
Summary The genes (rpo B/C1/C2) coding for the , , subnits of maize (Zea mays) chloroplast RNA polymerase have been located on the plastome and their nucleotide sequences established. The operon is part of a large inversion with respect to the tobacco and spinach chloroplast genomes and is flanked by the genes trnC and rps2. Notable features of the nucleotide sequence are the loss of an intron in rpoC1, and an insertion of approximately 450 by in rpOC2 compared to the dicotyledons tobacco, spinach and liver-wort. The derived amino acid sequence of this additional monocotyledon specific sequence is characterized by acidic heptameric repeat units containing stretches of glutamic acid, tyrosines and leucines with regular spacing. Other structural motifs, such as a nucleotide binding domain in the subunit and a zinc finger in the subunit, are compared at the amino acid level throughout the RNA polymerase subunits with the enzymes from other organisms in order to identify functionally important conserved regions.The sequence data presented in this paper will appear in the EMBL/Gen Bank/DDBJ Nucleotide Databases under the accession number X17318 相似文献
16.
Zusammenfassung Durch Untersuchung der Einwirkung von Röntgenstrahlen (50–200 kR) auf Carboxyl-14C-, 2-14C- und14CH3-markiertes Methionin sowie auf nicht radioaktivmarkiertes Methionin konnte festgestellt werden, daß folgende Umwandlungsprodukte entstehen: Methioninsulfoxyd (MSO),-Hydroxy--methylmercaptobuttersäure (HMMB),-Methylmercaptopropionsäure (MMP) und Homocystein (HO).MSO und die als Zwischenstufe vermutete-Methylmercapto--ketobuttersäure konnten nicht nachgewiesen werden. Außerdem wurde in keinem Versuch eine Abspaltung die S-CH3-Gruppe (z. B. zu-Aminobuttersäure) und eine Bildung von Methioninsulfon gefunden, die von anderen Autoren nach Einwirkung hoher Dosen beschrieben wurde. Bei einer Dosis 50 kR. konnte als Umwandlungsprodukt nur MSO festgestellt werden.Die Einwirkung von H2O2 auf Methionin liefert qualitativ die gleichen Umwandlungsprodukte, jedoch unterscheiden sich die Mengenverhältnisse der gebildeten Produkte deutlich von den Werten, die nach Bestrahlung erhalten werden.Der Deutschen Forschungsgemeinschaft danken wir für eine Sachbeihilfe. 相似文献
17.
Fumito Matsuura Masaya Ohta Khoichi Murakami Yujirou Matsuki 《Glycoconjugate journal》1993,10(3):202-213
Structures of the Asn linked oligosaccharides of quail egg-yolk immunoglobulin (IgY) were determined in this study. Asn linked oligosaccharides were cleaved from IgY by hydrazinolysis and labelled withp-aminobenzoic acid ethyl ester (ABEE) afterN-acetylation. The ABEE labelled oligosaccharides were then fractionated by a combination of Concanavalin A-agarose column chromatography and anion exchange, normal phase and reversed phase HPLC before their structures were determined by sequential exoglycosidase digestion, methylation analysis, HPLC, and 500 MHz1H-NMR spectroscopy. Quail IgY contained only neutral oligosaccharides of the following categories: the glucosylated oligomannose type (0.6%, Glc1-3Glc1-3Man9GlcNAc2; 35.6%, Glc1-3Man7–9GlcNAc2). oligomannose type (15.0%, with the structure Man5–9GlcNAc2) and biantennary complex type with core structures of-Man1-3(-Man1-6)Man1-4GlcNAc1-4GlcNAc (9.9%),-Man1-3(GlcNAc1-4)(-Man1-6)Man1-4GlcNAc1-4GlcNAc (25.1%) and-Man1-3(GlcNAc1-4)(-Man1-6)Man1-4GlcNAc1-4(Fuc1-6)GlcNAc (11.4%). Although never found in mammalian proteins, glucosylated oligosaccharides (Glc1Man7–9GlcNAc2) have been located previously in hen IgY.Abbreviations IgG, IgM, IgA, IgY
immunoglobulin G, M, A and Y, respectively
- ABEE
p-aminobenzoic acid ethyl ester 相似文献
18.
The crystal structure of mitochondrial F1-ATPase indicatesthat the and subunits fold into a structure defined by threedomains: the top -barrel domain, the middle nucleotide-binding domain,and the C-terminal -helix bundle domain (Abraham et al.1994); Bianchet et al., 1998). The -barrel domains of the and subunits form a crown structure at the top ofF1, which was suggested to stabilize it (Abraham et al.1994). In this study. the role of the -barrel domain in the and subunits of the yeast Saccharomyces cerevisiae F1,with regard to its folding and assembly, was investigated. The -barreldomains of yeast F1 and subunits were expressedindividually and together in Escherichia coli. When expressedseperately, the -barrel domain of the subunit formed a largeaggregate structure, while the domain of the subunit waspredominately a monomer or dimer. However, coexpression of the -barreldomain of subunit domain. Furthermore, the two domains copurified incomplexes with the major portion of the complex found in a small molecularweight form. These results indicate that the -barrel domain of the and subunits interact specifically with each other and thatthese interactions prevent the aggregation of the -barrel domain of the subunit. These results mimic in vivo results and suggest thatthe interactions of the -barrel domains may be critical during thefolding and assembly of F1. 相似文献
19.
Electrolyte leakage was measured in hardened and nonhardened leaves of three potato species, Solanum tuberosum L., S. acaule Bitt. and S. commersonii Dun., and one interspecific cross, Alaska Frostless (S. acaule x S. tuberosum) when exposed to various subzero temperatures. The leaves were undercooled (no ice present) from 0°C to -12.5°C for 45 min and to-4°C for up to 10 d. Regardless of the degree of undercooling no injury was observed in any of the potatoes, hardened or nonhardened, for up to 12 h. After 5 d, however, electrolyte leakage was observed in hardened S. tuberosum, S. acaule and S. commersonii, and in nonhardened Alaska Frostless. After 10 d exposure all potatoes, hardened and nonhardened, showed a significant amount of electrolyte leakage as compared to their controls kept at 0°C for 10 d.Scientific Journal Series Paper No. 13842 of the Minnesota Agricultural Experiment Station, St. Paul, Minn 相似文献
20.
Fumiaki Nakatsubo T. Kent Kirk Mikio Shimada Takayoshi Higuchi 《Archives of microbiology》1981,128(4):416-420
The degradation of the phenylcoumaran substructure model compound methyl dehydrodiconiferyl alcohol by the white-rot wood decay fungus Phanerochaete chrysosporium was investigated using culture conditions optimized for lignin oxidation. Initial attack was in the cinnamyl alcohol side chain, which was oxidized to a glycerol structure. This was subsequently converted by loss of the two terminal carbon atoms, C and C, to yield a C-aldehyde structure, which was further oxidized to the C-acid compound. The next detected intermediate, a phenylcoumarone, was produced by double bond formation between C and C, and oxidation of the C-alcohol to an aldehyde group. Further oxidation of C to an acid yielded the next intermediate. The final identified degradation product was veratric acid. No products from the 5-substituted aromatic ring, and no phenolic products, were found. The initial glycerol-containing intermediate was a mixture of the threo and erythro forms, and no optical activity could be found, suggesting that its formation might have involved nonstereospecific C-C epoxidation followed by non-enzymatic hydrolysis of the epoxide.Abbreviations TLC
thin layer chromatography
- LDA
lithium diisopropyl amide
- DDQ
2,3-dichloro-5,6-dicyanobenzoquinone
- MS
mass spectrometry
- UV
ultraviolet spectroscopy 相似文献