Abstract: A touch display screen and a touch display apparatus are disclosed. The touch display screen comprises: an array substrate and a color film substrate disposed box to box; a group of first electrode lines disposed on the array substrate or the color film substrate; a group of second electrode lines disposed on the array substrate or the color film substrate and arranged as crossing the group of first electrode lines; a conductive shielding layer with high-resistance transparency, disposed on the color film substrate and located above the group of first electrode lines and the group of second electrode lines. Because the resistance value of the conductive shielding layer with high resistance and transparency is high, a projected field signal between the first electrode lines and the second electrode lines may pass through the conductive shielding layer to ensure a realizability of touch operations.

Abstract: The present disclosure provides a capacitive in-cell touch panel and a display apparatus, wherein touch sensing electrodes are set on a color filter substrate, a common electrode layer connected as a whole plane on a TFT array substrate is divided into strips to be used as touch driving electrodes, and metal driving electrodes directly electrically connected to the corresponding touch driving electrodes are set on the TFT array substrate so as to reduce resistance of the touch driving electrodes. The embodiments of the disclosure can save the production cost and improve the production efficiency. Moreover, the touch function and the display function are driven in a time division manner, and thus the production cost can be further reduced, and the picture quality and touch accuracy can be enhanced.

Abstract: Embodiments of the present invention disclose a capacitive in-cell touch panel, a driving method thereof and a display device. Touch sensing electrodes extended along the row direction of pixel units are arranged on a color filter substrate; a thin-film transistor (TFT) array substrate adopts a dual gate structure, that is, two gate signal lines are disposed between every two adjacent rows of pixel units; every two adjacent columns of pixel units are taken as a group of pixel unit columns and share a data signal line disposed between the two pixel unit columns, so that the positions of a part of data signal lines can be saved; and touch driving electrodes for achieving the touch function are arranged at the saved positions of the data signal lines.

Abstract: A capacitive in cell touch panel, its driving method and a display device, in which, on the TFT array substrate, a pixel structure in which two adjacent rows of pixel units form one pixel unit group and two gate signal lines are disposed between the two rows of pixel units of the pixel unit group is adopted. Positions of gate signal lines between adjacent pixel unit groups can be saved by modifying positions of gate signal lines of two adjacent rows of pixel units and TFT switches. As such, touch driving lines with touch function can be set at the saved positions for gate signal lines and touch sensing electrodes can be disposed on the color filter substrate and extend in the column direction of the pixel units to realize touch function while ensuring high aperture ratio.

Abstract: The present invention discloses a capacitive in cell touch panel and display device, wherein touch sensing electrodes are provided on a color filter substrate, the whole common electrode layer of the TFT array substrate is segmented into a plurality of strip-shaped structures functioning as touch driving electrodes, and the touch driving electrodes are driven in a time-sharing manner to achieve the touch function and the display function in a time-sharing manner. Since in the touch panel according to the present invention, structure of the common electrode layer of the TFT array substrate is altered to form the touch driving electrodes, it is not necessary to add a new film on the existing TFT array substrate and only an additional process needs to be added to segment the whole common electrode layer into a plurality of strip-shaped structures, reducing the production cost and increasing the production efficiency.

Abstract: A capacitive in-cell touch screen panel and a display apparatus are disclosed in present disclosure. At least one touch control inducting electrode is disposed on the color film substrate and at least one touch control driving electrode is disposed on the TFT array substrate. Each of the touch control driving electrodes overlaps with multiple sets of gate lines in the TFT array substrate, respectively, and each of the touch control driving electrodes comprises touch control driving sub-electrodes disposed along the row direction and a driving control unit is disposed at the connection of each of the touch control driving sub-electrodes and each set of gate lines.

Abstract: An embodiment of the disclosure discloses an in-cell touch panel having advantages such as a simple structure and a low cost. The in-cell touch panel comprises: a first substrate and a second substrate arranged oppositely, wherein a plurality of gate lines arranged horizontally are formed on the first substrate; the in-cell touch panel further comprises: a plurality of touch driving lines arranged horizontally; a plurality of touch sensing lines arranged vertically; and a plurality of touch scanning TFTs, wherein each touch scanning TFT has a gate connected to one gate line, a source connected to a touch driving circuit, and a drain connected to one touch driving line, the one gate line is only connected to the gate of one touch scanning TFT; wherein, the number of the gate lines?the number of the touch scanning TFTs?the number of the touch driving lines.

Abstract: The present invention relates to genetically engineered micro-organisms for the combined production of 1,3-propanediol (PDO), 2,3-butanediol (BDO), and polyhydroxypropionic acid (PHP) by fermentation. In particular, the invention relates to a genetically engineered micro-organism suitable for combined production of PDO, BDO and PHP by fermentation, characterized in that: compared with corresponding wild-type starting micro-organism, the D-lactate dehydrogenase gene in the genetically engineered micro-organism is deleted or functionally inactivated, and the genetically engineered micro-organism comprises a heterogenous polynucleotide encoding the Coenzyme A-dependent Aldehyde dehydrogenase and a heterogenous polynucleotide encoding the Polyhydroxyalkanoate synthase. Methods for the construction of such micro-organisms, and methods for combined production of PDO, BDO and PHP by fermentation of a genetically engineered bacterium are also taught.

Abstract: The invention discloses a method for producing 1,3-propanediol, comprising the steps of: using crude glycerol, a by-product during the biodiesel production, without further treatment, as the substrate for production of 1,3-propanediol; inoculating a 1,3-propanediol-producing strain in a seed medium containing crude glycerol, a by-product from biodiesel production; adding the seed culture into a fermentation medium containing crude glycerol, a by-product from biodiesel production, and fermenting; maintaining pH in a range of 6.8 to 8.0; and in the end of the fermentation, isolating and purifying 1,3-propanediol.

Abstract: The present invention relates to genetically engineered micro-organisms for the combined production of 1,3-propanediol (PDO), 2,3-butanediol (BDO), and polyhydroxypropionic acid (PHP) by fermentation. In particular, the invention relates to a genetically engineered micro-organism suitable for combined production of PDO, BDO and PHP by fermentation, characterized in that: compared with corresponding wild-type starting micro-organism, the D-lactate dehydrogenase gene in the genetically engineered micro-organism is deleted or functionally inactivated, and the genetically engineered micro-organism comprises a heterogenous polynucleotide encoding the Coenzyme A-dependent Aldehyde dehydrogenase and a heterogenous polynucleotide encoding the Polyhydroxyalkanoate synthase. Methods for the construction of such micro-organisms, and methods for combined production of PDO, BDO and PHP by fermentation of a genetically engineered bacterium are also taught.

Abstract: The present invention relates to genetically engineered micro-organisms for the combined production of 1,3-propanediol (PDO), 2,3-butanediol (BDO), and polyhydroxypropionic acid (PHP) by fermentation. In particular, the invention relates to a genetically engineered micro-organism suitable for combined production of PDO, BDO and PHP by fermentation, characterized in that: compared with corresponding wild-type starting micro-organism, the D-lactate dehydrogenase gene in the genetically engineered micro-organism is deleted or functionally inactivated, and the genetically engineered micro-organism comprises a heterogenous polynucleotide encoding the Coenzyme A-dependent Aldehyde dehydrogenase and a heterogenous polynucleotide encoding the Polyhydroxyalkanoate synthase. Methods for the construction of such micro-organisms, and methods for combined production of PDO, BDO and PHP by fermentation of a genetically engineered bacterium are also taught.

Abstract: The invention discloses a method for producing 1,3-propanediol and 2,3-butanediol from raw starch materials, including the following steps: 1) Candida krusei or Hansenula Arabitolgens Fang are inoculated into a fermentation medium with the saccharifying liquid of the raw starches as a carbon source; the yeast cells are cultured on an aerobic condition until glucose-consuming-rate is significantly reduced, and then fermented anaerobically to a glucose concentration from 5 to 10 g/L; the fermentation broth is collected and filtered to remove the yeast cells in the broth, and the resultant filtrate is glycerin fermentation broth; 2) Klebsiella, Clostridium butyricum, or Clostridium pasteurianum are inoculated into a fermentation medium in which the glycerin fermentation broth obtained from step 1) serves as a carbon source; the bacteria are fermented anaerobically for 30-32 hours, and then fermented aerobically when the production rate of 1,3-propanediol decreased obviously, and the fermentation was stopped when

Abstract: The present invention relates to methods and genetically engineered micro-organisms for the combined production of PDO, BDO, and PHP by fermentation. The micro-organism is characterized in that its D-lactate dehydrogenase gene has been deleted or functionally inactivated, and it comprises heterogenous polynucleotides encoding the Coenzyme A-dependent Aldehyde dehydrogenase and the Polyhydroxyalkanoate synthase.

Abstract: The invention discloses a method for producing 1,3-propanediol, comprising the steps of: using crude glycerol, a by-product during the biodiesel production, without further treatment, as the substrate for production of 1,3-propanediol; inoculating a 1,3-propanediol-producing strain in a seed medium containing crude glycerol, a by-product from biodiesel production; adding the seed culture into a fermentation medium containing crude glycerol, a by-product from biodiesel production, and fermenting; maintaining pH in a range of 6.8 to 8.0; and in the end of the fermentation, isolating and purifying 1,3-propanediol.

Abstract: The invention discloses a method for producing 1,3-propanediol and 2,3-butanediol from raw starch materials, including the following steps: 1) Candida krusei or Hansenula Arabitolgens Fang are inoculated into a fermentation medium with the saccharifying liquid of the raw starches as a carbon source; the yeast cells are cultured on an aerobic condition until glucose-consuming-rate is significantly reduced, and then fermented anaerobically to a glucose concentration from 5 to 10 g/L; the fermentation broth is collected and filtered to remove the yeast cells in the broth, and the resultant filtrate is glycerin fermentation broth; 2) Klebsiella, Clostridium butyricum, or Clostridium pasteurianum are inoculated into a fermentation medium in which the glycerin fermentation broth obtained from step 1) serves as a carbon source; the bacteria are fermented anaerobically for 30-32 hours, and then fermented aerobically when the production rate of 1,3-propanediol decreased obviously, and the fermentation was stopped when