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Method of determining the permeability of an underground medium from NMR logs of the permeability of rock fragments from the medium, based on prior calibration of the permeability resulting from these measurements, from direct measurements on rock fragments such as cuttings for example. The method mainly comprises measuring permeability (k) from rock fragments, measuring the signal produced by a device allowing NMR analysis of the rock fragments previously saturated with a protonated liquid (brine for example), obtaining optimum values for the parameters of a relation giving the permeability as a function of the NMR signal, and applying this relation to the well zones that have already been subjected to NMR logging but for which no direct permeability measurements are available. Applications: evaluation of a hydrocarbon reservoir for example.

Provided is a light-switchable gene expression system, comprising: a) a recombinant light-switchable transcription factor-encoding gene, said recombinant light-switchable transcription factor comprising a first polypeptide as the DNA bonding domain, a second polypeptide as the photosensitive domain, and a third polypeptide as the transcription regulatory domain; b) a target transcription unit comprising at least one reaction element recognized and bound by the first polypeptide, a promoter regulated by the third polypeptide and a nucleotide sequence to be transcribed. Also provided is an eukaryotic expression vector comprising said light-switchable gene expression system, and a method for regulating gene expression in a host cell by using the light-switchable gene expression system. Also provided is a reagent kit containing different elements of the light-switchable gene expression system. The light-switchable gene expression system has a quick, effective and powerful induction with little or no toxicity. It is safer than other inducers, and can spatiotemporally control gene expression.

A method of preparing a three-dimensional composite material includes the following steps: preparing polystyrene by soap-free emulsion polymerizing, obtaining polystyrene opal by a vertical deposition method, synthesizing MoP IO (molybdenum phosphide inverse opal), and compounding with quantum points CdS, so as to obtain a novel inorganic composite material, namely cadmium sulfide quantum dot-compounded MoP IO. The preparation method has the advantages that the MoP IO is prepared first, and the MoP IO is of a three-dimensional cyclic pore structure and has the photonic band gap feature, so that the MoP IO has better catalysis effect in light catalysis in comparison with that of common porous material; the MoP IO is compounded with the cadmium sulfide quantum dots, so that the light absorbing ability is enhanced, and the composite material capable of absorbing the visible light is obtained.

Provided is an optically controlled gene expression system of prokaryotic bacterium, comprising: a) a photosensitive recombinant transcription factor encoding gene, the photosensitive recombinant transcription factor is one fusion protein comprising a first polypeptide as the DNA bonding domain and a second polypeptide as the photosensitive domain; b) a target transcription unit comprising promoter or promoter-reaction element or reaction element-promoter containing at least one reaction element recognized/bound by the first polypeptide and the nucleic acid sequence to be transcribed. Also provided is a prokaryotic expression vector comprising said optically controlled gene expression system, and a method for regulating gene expression in a prokaryotic host cell by using the optically controlled gene expression system. Also provided is a reagent kit containing different components of the optically controlled gene expression system. The optically controlled gene expression system of prokaryotic bacterium has a quick, effective and powerful induction, is safer than other inducers, is of little or no toxicity, and can control gene expression both spatially and temporally, and can regulate many life processes of prokaryotic bacterium.

A method of preparing hollow molybdate composite microspheres includes steps of: (1) dissolving 1-4 mmol of MCl₂ in 20 ml of water to obtain a solution A and dissolving 1-4 mmol. of molybdic acid in 20 ml of water to obtain a solution B, followed by mixing the solution A and the solution B, in which M is Co, Ni, or Cu; (2) dissolving 10-40 mmol of urea in 40 ml of water, adding the mixed solution of step (1) and stirring uniformly; (3) placing the mixed solution of step (2) into a reaction vessel and reacting at 120-160° C. for 6-12 hours; (4) suction filtrating and water washing, followed by drying in a vacuum oven at 40-60° C.; (5) calcination at 350-500° C. for 2-4 hours in a Muffle furnace.

A NaY molecular sieve with an aluminum-rich surface is prepared using a process that includes the steps of: a. mixing a directing agent and a first silicon source to obtain a first mixture, wherein the directing agent has a molar composition of Na₂O: Al₂O₃: SiO₂: H₂O=(6-25): 1: (6-25): (200-400); b. mixing the first mixture obtained in the step a with a second silicon source, an aluminum source and water to obtain a second mixture; c. carrying out hydrothermal crystallization on the second mixture obtained in the step b, and collecting a solid product. Calculated as SiO₂, the weight ratio of the first silicon source to the second silicon source is 1: (0.01-12). The NaY molecular sieve has larger aluminum distribution gradient from the surface to the center of the particle than the conventional molecular sieve.

Packaging bag (100) comprising a pouch (1) for storing at least one substance, said pouch (1) being provided with an outlet (2) for extracting the substance and with inner layers (6a, 6b) partly attached to the pouch (1) and partly detached from said pouch (1) so to leave free strips (8a, 8b) at the outlet (2), said free strips (8a, 8b) being joinable together to obtain a sealed membrane (11) for closing a fillable aseptic housing (9) storing the substance, a spout (13) being located off said aseptic housing (9) and fixed to the pouch (1).

A resolution method of axial chiral enantiomers of lesinurad (2-(5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-ylthio)acetic acid) adopts inexpensive and readily available quinoline natural products and derivatives thereof, such as quinine, cinchonine, quinidine or cinconidine as resolving agents to react with lesinurad racemate in an organic solvent to form a salt, and the salt is dissociated by acidification so as to obtain optically pure (R)- or (S)-2-(5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-ylthio)acetic acid. The method can give axial chiral enantiomer of lesinurad in R configuration with a chiral purity ee of up to 100% and a total yield of 90% or more. The obtained axial chiral enantiomer of lesinurad in S configuration can reach a chiral purity ee of up to 99.9% and a total yield of 80% or more.

The invention discloses an arylpyrrolecarbonitrile compound for insecticidal use, a preparation method and use thereof, an agricultural insecticide and a method for controlling pests. The preparation method comprises the following preparation steps: (1) 2-p-chlorophenyl-4-bromo-5-trifluoromethyl-3-cyanopyrrole, 2-chloro-5-chloromethylthiazole and potassium carbonate are provided as reaction starting materials in a ratio of the amount of substance of 1:1:1.2, and starting materials are put into a three-necked bottle together with DMF; (2) the materials are reacted at 60 to 100° C. for 1 to 4 hours; (3) the reaction is stopped after the completion of the reaction of the starting materials is detected, the materials are cooled to room temperature and filtered by suction to give 4-bromo-2-(4-chlorophenyl)-1-(2-chloro-5-thiazolylmethyl)-5-trifluoromethylpyrrole-3-carbonitrile as a white solid. The compound of the invention has a simple synthesis route, the needed starting materials are cheap and easy to obtain, the product has low production cost and has excellent broad-spectrum insecticidal activity against such plants as rice, cabbage and tomato.

A sensor cartridge has a cartridge substrate comprising an optical substrate for optical detection of a target moiety in a sample fluid based on frustrated totalinternal reflection and at least one electric structure. This way, optical read-out and electrical functions, e.g. read-out, are combined in a single substrate, in a simple and cheap manner. Also a method of fabricating such sensor cartridge is provided.