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51.
Silva Silvio S. Ribeiro JoÃo D. Felipe Maria G. A. Vitolo Michelle 《Applied biochemistry and biotechnology》1997,(1):557-564
Batch fermentations of sugar cane bagasse hemicellulosic hydrolysate treated for removing the inhibitors of the fermentation
were performed byCandida guilliermondii FTI20037 for xylitol production. The fermentative parameters agitation and aeration rate were studied aiming the maximization
of xylitol production from this agroindustrial residue. The maximal xylitol volumetric productivity (0.87 g/L h) and yield
(0.67 g/g) were attained at 400/min and 0.45 v.v.m. (KLa 27/h). According to the results, a suitable control of the oxygen input permitting the xylitol formation from sugar cane
bagasse hydrolysate is required for the development of an efficient fermentation process for large-scale applications. 相似文献
52.
Zanin Gisella M. Neitzel Ivo De Moraes Flavio F. 《Applied biochemistry and biotechnology》1993,(1):477-489
The axial dispersion of a liquid fluidized bed of controlled pore silica (CPS) particles has been determined by the pulse
tracer method. The CPS used was the same as for enzyme immobilization, having an average diameter of 0.436 mm and mean pore
size of 37.5 nm. The fluidization liquid is α-amylase liquefied manioc starch, 30% w/v, 45°C pH=4.5. Nominal bed porosities
tested were 0.7 and 0.8. The results show that the axial dispersion coefficient increases with greater superficial liquid
velocities. Various available correlations tested disagree with each other to a large extent and are unable to represent collected
experimental data. 相似文献
53.
Attempts to miniaturize electrophoresis (EP) to save time or enhance productivity and efficiency remains a challenge for science
and industry. Other advantages of miniaturization include: increased sensitivity, saving of reagents, greater yield of data,
and enabling studies where only small samples are available. Since electrophoresis that takes hours may be reduced to a matter
of minutes, the limitations of miniaturization in clinical, industrial, and research applications are evaluated. Clinical
electrophoresis (EP) on cellulose acetate media can be performed in 3.5 min instead of 20–45 min and on SDS polyacrylamide
gels in 15–30 min compared with conventional 3–8 h. 相似文献
54.
Comparison of different strains of the yeastYarrowia lipolytica for citric acid production from glucose hydrol 总被引:3,自引:0,他引:3
Maria Wojtatowicz Waldemar Rymowicz Helena Kautola 《Applied biochemistry and biotechnology》1991,31(2):165-174
Four commercial strains and two mutants of the yeast species Yarrowia lipolytica were screened using batch fermentation. Strain Y. lipolytica A-101-1.14 (induced with UV irradiation) was found to be the most suitable for citric acid production from glucose hydrol (39.9% glucose and 2.1% other sugars), a byproduct of glucose production from potato starch. The specific rate of total citric and isocitric acid production was 0.138 g/g.h, the yield on consumed glucose 0.93 g/g, and the productivity achieved was as high as 1.25 g/L.h. All of the tested yeast strains were able to utilize only the glucose from the glucose hydrol medium. Thus, some residual higher oligosaccharides remained in the process effluent. 相似文献
55.
Owen S. Jeong B. C. Poole P. S. Macaskie L. E. 《Applied biochemistry and biotechnology》1992,(1):693-707
Tributyl phosphate (TBP), a plasticizer and solvent, is used in nuclear fuel reprocessing, generating TBP wastes laden with
residual uranium. ACitrobacter sp. accumulated heavy metals via a phosphohydrolase(s) that precipitated metals with inorganic phosphate liberated from an
organic phosphate “donor” molecule (TBP). Mutant analysis suggested that TBP hydrolysis was not attributable to a previously
documented acid phosphatase (monoesterase). Purified monoesterase had little activity against phospho di- and triesters, had
no requirement for Mg2+ or Mn2+, and was EDTA-resistant. Conversely, TBP cleavage by immobilized cells was enhanced by Mg2+, and ininhibited by Mn2+ and EDTA. A separate phosphotri/diesterase was implicated. 相似文献
56.
Two amino acid analog resistant mutants of the cyanobacteriumAnabaena sp 287 were isolated after MNNG mutagenesis.Anabaena ST 16, a mutant resistant to the alanine analog D-α-aminobutyric acid andAnabaena ST 25, another mutant resistant to the histidine analog l,2,4-triazole-3-alanine, released alanine and histidine, respectively,
into the medium upon immobilization in alginic acid during diazotrophic growth in fluidized bed reactors. The rates of amino
acid production by the mutants were 4.3 μmol mg chl-1 h-1 of D-alanine byAnabaena ST 16 and 16.6 μnol mg chl-1 h-1 of L-histidine byAnabaena ST 25. Nitrogen fixation by the mutants was not affected by the extracellular amino acid concentration. While the radioactive
carbon flow was followed, the parent strain retained 93% of fixed14C and released only 7% into the medium. On the other hand,Anabaena ST 16 released 13% andAnabaena ST 25 released 29% into the medium. These mutants are beneficial in the production of radioactive amino acids using diazotrophic
photobiotechnology. 相似文献
57.
The growth ofBacillus amyloliquefaciens in the aqueous two-phase system, made up of polyethylene glycol, dextran, and water, was investigated. Generally,Bacillus partitions in the dextran phase, but the magnitude of the separation depends largely on the overall composition of polymers
in the phase system. The kinetics of growth ofBacillus amyloliquefaciens was studied in the polyethylene glycol-rich continuous phase, dextran-rich dispersed phase, and in the mixed phase. From
the kinetic data it appears that increasing the overall polymer composition causes the cells to adsorp at the interface. On
the other hand, partition measurements indicate that increasing polymer concentrations make the cell partitioning more one-sided.
This anomaly is explained by studying the interfacial adsorption of cells via dynamic surface tension measurements. 相似文献
58.
Kaster Jeffrey A. Michelsen Donald L. Velander William H. 《Applied biochemistry and biotechnology》1990,(1):469-484
A microbubble dispersion (MBD) was used to supply oxygen for aerobic fermentations in a standard 2 L stirred tank fermenter.
The microbubble dispersion was formed using only surfactants produced naturally. Growth rates ofSaccharomyces cerevisiae cultures were found to be equal or greater with MBD sparging than with gas sparging. The oxygen transfer coefficent with
MBD sparging was found to be 190/h and independent of impeller speed from 100–580 rpm. The oxygen transfer coefficient with
air sparging rose from 55 to 132/h over the same range of impeller speeds. Power requirements for the fermenter systems were
estimated. 相似文献
59.
Nguyen Huyen Rao A. Madhusudhan Phillips J. B. John Vijay T. Reed Wayne F. 《Applied biochemistry and biotechnology》1991,(1):843-853
We describe a technique to modify protein solubility and optimize enzyme activity in reversed micellar solutions. The technique
is based on the ability of hydrates of natural gas to form in the micro-aqueous phase. Clathrate hydrates are crystalline
inclusions of water and gas, and their formation in bulk water has traditionally been studied with relevance to natural gas
recovery. We have found that hydrates can form in the environment of the microaqueous pools of reversed micelles, and that
their extent of formation can be well controlled through the thermodynamic variables of temperature and pressure. Additionally,
formation of hydrates affects the size and aggregation number of the micelles, and thus influences the solubility and conformation
of encapsulated proteins. We demonstrate how the concept can be used in two applications: (i) protein extraction into reversed
micelles and subsequent recovery, and (ii) optimization of enzyme activity in reversed micelles. 相似文献
60.
A starter culture ofTrichoderma reesei (Rut-C30) prepared in a liquid fluidized bed reactor (LFBR) gave better growth and greater cellulase production in submerged
fermentation than a conventional shake flask inoculum. The LFBR starter was prepared by first coatingT. reesei spores to 0.25 mm size corncob (1.0x108g-1) in a medium containing 1.0% corncob, 0.5 gL-1 xylose and 0.1 gL-1 lactose in a balanced salt solution, then fluidizing the particles in the LFBR for 36 h to allow germination of the spores,
and covering the particles with an approx 30 μm thick biofilm. This biofilm that developed in constant adherence to the lignocellulosic
carrier, apparently became well adapted to grow rapidly on insoluble cellulose substrates (Solca Floc), and had the enzymes
of the cellulase complex induced for increased cellulase production.
The LFBR starter used in a stirred tank reactor (STR) gave 15 gL-1 biomass production and 6.5 IU mL-1 overall cellulase activity with a volumetric productivity of 64 IU L-1h-1 in a 5 d fermentation, compared with a 7 d shake flask inoculum that gave 11 gL-1 biomass and 3.2 IU mL-1 cellulase activity, with a volumetric productivity of 31IU L-1h-1. The LFBR starter culture retained its viability in dry storage for 6–9 mo. 相似文献