Optical fourier processing
    1.
    发明授权
    Optical fourier processing 失效
    光学加工

    公开(公告)号:US5854710A

    公开(公告)日:1998-12-29

    申请号:US709994

    申请日:1996-09-09

    CPC分类号: G02B5/23 G02B27/46 G03H1/16

    摘要: The invention relates to systems and methods for optical Fourier processing and logic operations based on the discovery that the photoinduced anisotropy of photochromic materials such as bacteriorhodopsin, organic fulgides, azo and fluorescent dyes, phycobiliproteins, rhodopsins, and their analogs, is dependent on the intensity of a polarized actinic beam that illuminates the material and the intensity profile of one or more input beams. This intensity dependence can be used to implement a simple, real-time, self-adaptive optical processing, i.e., spatial filtering, system for Fourier processing of optical input images. This optical processing system can be used to process a wide variety of optical input images, from projected still images to live motion picture images.

    摘要翻译: 本发明涉及用于光学傅立叶处理和逻辑运算的系统和方法,其基于以下发现:光致变色材料如细菌视紫红质,有机游离基,偶氮和荧光染料,藻胆蛋白,视紫红质及其类似物的光致各向异性取决于强度 的一个偏振光束,其照亮一个或多个输入光束的材料和强度分布。 该强度依赖性可以用于实现简单的实时自适应光学处理,即用于光输入图像的傅立叶处理的空间滤波系统。 该光学处理系统可以用于处理从投影的静止图像到活动电影图像的各种各样的光学输入图像。

    Enzyme-catalyzed modifications of macromolecules in organic solvents
    3.
    发明授权
    Enzyme-catalyzed modifications of macromolecules in organic solvents 失效
    大分子在有机溶剂中的酶催化修饰

    公开(公告)号:US06210936B1

    公开(公告)日:2001-04-03

    申请号:US09165043

    申请日:1998-10-01

    IPC分类号: C12P762

    CPC分类号: C12P7/625

    摘要: Protease enzyme from Bacillus subtilis and Bacillus sp. Catalyzes the acylation of organic solvent-insoluble macromolecules in isooctane solution containing vinyl esters of fatty acids, lactones or lactides as acyl donors. The reaction occurs only when the enzyme is solubilized via ion-pairing with the anionic surfactant dioctylsulfosuccinate, sodium salt (AOT). Enzyme based acylation was demonstrated in macromolecules such as silk proteins. These macromolecules are reactive either as cryogenically milled powder suspended in the organic solvent or as a thin film deposited onto ZnSe slides. This selective acylation approach represents the first attempt at using enzymes to modify organic-insoluble macromolecules in nonaqueous media.

    摘要翻译: 来自枯草芽孢杆菌和芽孢杆菌的蛋白酶 催化有机溶剂不溶性大分子在含有脂肪酸,内酯或丙交酯的乙烯基酯作为酰基供体的异辛烷溶液中的酰化反应。 仅当酶通过与阴离子表面活性剂二辛基磺基琥珀酸盐钠盐(AOT)的离子配对溶解时才发生反应。 在大分子如丝蛋白中证明了酶的酰化作用。 这些大分子作为悬浮在有机溶剂中的低温研磨粉末或沉积在ZnSe载片上的薄膜是反应性的。 这种选择性酰化方法代表了在非水介质中使用酶来修饰有机不溶性大分子的第一次尝试。

    Enzyme-catalyzed modifications of macromolecules in organic solvents

    公开(公告)号:US06448050B1

    公开(公告)日:2002-09-10

    申请号:US09639412

    申请日:2000-08-14

    IPC分类号: C12P762

    CPC分类号: C12P7/625

    摘要: Protease enzyme from Bacillus subtilis and Bacillus sp. Catalyzes the acylation of organic solvent-insoluble macromolecules in isooctane solution containing vinyl esters of fatty acids, lactones or lactides as acyl donors. The reaction occurs only when the enzyme is solubilized via ion-pairing with the anionic surfactant dioctylsulfosuccinate, sodium salt (AOT). Enzyme based acylation was demonstrated in macromolecules such as silk proteins. These macromolecules are reactive either as cryogenically milled powder suspended in the organic solvent or as a thin film deposited onto ZnSe slides. This selective acylation approach represents the first attempt at using enzymes to modify organic-insoluble macromolecules in nonaqueous media.

    Enzyme-catalyzed synthesis of macromolecules in organic solvents
    7.
    发明授权
    Enzyme-catalyzed synthesis of macromolecules in organic solvents 失效
    有机溶剂中大分子的酶催化合成

    公开(公告)号:US5981240A

    公开(公告)日:1999-11-09

    申请号:US173607

    申请日:1998-10-02

    IPC分类号: C12P7/62 C12N9/50

    CPC分类号: C12P7/625

    摘要: A method is described for a simple, fast and efficient synthesis of homopolymers and copolymers by the enzymatic ring opening polymerization of lactones and lactides. The enzyme used is an ion paired protease. The advantage of this enzymatic system is in using small amount of enzyme per monomer and lower reaction time. Homopolymers and copolymers are synthesized with molecular weights between 1000 and 4600 daltons, and dispersity as low as 1.1. The monomer conversion after 4 days, for reactions catalyzed by protease S, has reached 100%. Different initiators are used to control the rate and degree of polymerization. Synthesis of block copolymers with defined block size and crystallinity are described in this invention. These biodegradable and bioerodable polyesters and copolyesters with controlled molecular weight, dispersity and crystallinity have applications in medical, drug, cosmetic and food industries.

    摘要翻译: 描述了通过内酯和丙交酯的酶开环聚合简单,快速和有效地合成均聚物和共聚物的方法。 使用的酶是离子配对蛋白酶。 该酶系统的优点在于每单体使用少量酶,反应时间较短。 合成均聚物和共聚物的分子量为1000至4600道尔顿,分散度低至1.1。 4天后,由蛋白酶S催化反应的单体转化率达到100%。 不同的引发剂用于控制聚合速率和聚合度。 本发明描述了具有确定的嵌段大小和结晶度的嵌段共聚物的合成。 这些具有可控分子量,分散性和结晶度的可生物降解和生物侵蚀性聚酯和共聚酯可用于医疗,药物,化妆品和食品工业。

    Chemiluminescence-based method for rapid and sensitive in-situ detection
of organophosphorus compounds and metal ions
    8.
    发明授权
    Chemiluminescence-based method for rapid and sensitive in-situ detection of organophosphorus compounds and metal ions 失效
    基于化学发光的方法,用于快速和灵敏地原位检测有机磷化合物和金属离子

    公开(公告)号:US5846753A

    公开(公告)日:1998-12-08

    申请号:US445565

    申请日:1995-05-30

    IPC分类号: C12Q1/42 C07D305/14 C12Q1/44

    CPC分类号: C12Q1/42 C12Q2334/00

    摘要: A method of detecting the presence of a substance being monitored in a medium, selected from the group of substances including organophosphorus compounds and the metal ions Zn, Be and Bi, including the steps of: providing a 1,2-dioxetane phenyl phosphate compound; providing a phosphatase that catalytically degrades the 1,2-dioxetane phenyl phosphate compound to produce light, the catalytic activity of the phosphatase toward 1,2-dioxetane phenyl phosphate compound being altered by the substance being monitored; exposing the 1,2-dioxetane phenyl phosphate compound and the phosphatase together to a medium which may contain the substance being monitored; detecting light produced after the exposing step; and determining, from the detected light, the presence and concentration in the medium of the substance being monitored.

    摘要翻译: 一种检测在包括有机磷化合物和金属离子Zn,Be和Bi的物质组中的介质中被监测物质的存在的方法,包括以下步骤:提供1,2-二氧环乙烷苯基磷酸酯化合物; 提供催化降解1,2-二氧杂环丁烷苯基磷酸酯化合物以产生光的磷酸酶,磷酸酯对正在监测的物质的1,2-二氧环乙烷苯基磷酸酯化合物的催化活性改变; 将1,2-二氧环乙烷苯基磷酸酯化合物和磷酸酶一起暴露于可能含有被监测物质的介质中; 检测曝光步骤后产生的光; 并且从检测到的光中确定被监测物质的介质中的存在和浓度。

    Enzyme-catalyzed modifications of macromolecules in organic solvents
    10.
    发明授权
    Enzyme-catalyzed modifications of macromolecules in organic solvents 失效
    大分子在有机溶剂中的酶催化修饰

    公开(公告)号:US06455285B1

    公开(公告)日:2002-09-24

    申请号:US09639411

    申请日:2000-08-14

    IPC分类号: C12P762

    CPC分类号: C12P7/625

    摘要: Protease enzyme from Bacillus subtilis and Bacillus sp. Catalyzes the acylation of organic solvent-insoluble macromolecules in isooctane solution containing vinyl esters of fatty acids, lactones or lactides as acyl donors. The reaction occurs only when the enzyme is solubilized via ion-pairing with the anionic surfactant dioctylsulfosuccinate, sodium salt (AOT). Enzyme based acylation was demonstrated in macromolecules such as silk proteins. These macromolecules are reactive either as cryogenically milled powder suspended in the organic solvent or as a thin film deposited onto ZnSe slides. This selective acylation approach represents the first attempt at using enzymes to modify organic-insoluble macromolecules in nonaqueous media.

    摘要翻译: 来自枯草芽孢杆菌和芽孢杆菌的蛋白酶 催化有机溶剂不溶性大分子在含有脂肪酸,内酯或丙交酯的乙烯基酯作为酰基供体的异辛烷溶液中的酰化反应。 仅当酶通过与阴离子表面活性剂二辛基磺基琥珀酸盐钠盐(AOT)的离子配对溶解时才发生反应。 在大分子如丝蛋白中证明了酶的酰化作用。 这些大分子作为悬浮在有机溶剂中的低温研磨粉末或沉积在ZnSe载片上的薄膜是反应性的。 这种选择性酰化方法代表了在非水介质中使用酶来修饰有机不溶性大分子的第一次尝试。