天津科技大學(xué)生物工程學(xué)院導(dǎo)師:劉逸寒

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天津科技大學(xué)生物工程學(xué)院導(dǎo)師:劉逸寒

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天津科技大學(xué)生物工程學(xué)院導(dǎo)師:劉逸寒 正文

[導(dǎo)師姓名]
劉逸寒

[所屬院校]
天津科技大學(xué)

[基本信息]
導(dǎo)師姓名:劉逸寒
性別:男
人氣指數(shù):1769
所屬院校:天津科技大學(xué)
所屬院系:生物工程學(xué)院
職稱:副教授
導(dǎo)師類型:
招生專業(yè):藥理學(xué)
研究領(lǐng)域:[1]酶制劑開發(fā)與應(yīng)用:酶分子的挖掘與進(jìn)化,酶基因高效表達(dá)系統(tǒng)的構(gòu)建與優(yōu)化,酶蛋白發(fā)酵工藝...

[通訊方式]
辦公電話:022-60601958
電子郵件:lyh@tust.edu.cn
通訊地址:天津經(jīng)濟(jì)技術(shù)開發(fā)區(qū)第十三大街29號天津科技大學(xué)生物工程學(xué)院

[個(gè)人簡述]
代表性專利:[1] 劉逸寒,路福平,樊帥,徐艷靜,胡博,王春霞,王建玲.一種耐酸性高溫α-淀粉酶及其基因工程菌和制備方法,ZL201210246909.6.[2] 劉逸寒,王正祥,路福平,王春霞,王建玲.一種耐高溫α-淀粉酶及其制備方法和應(yīng)用,ZL201510004498.3.[3] 劉逸寒,路福平,薄嘉鑫,王春霞,王建玲.一種細(xì)胞表面展示磷脂酶D酵母全細(xì)胞催化劑催化制備磷脂酰絲氨酸的方法,ZL201110206069.6.[4] 路福平,劉逸寒,張濤,劉曉光,王正祥,王春霞,王建玲.一種磷脂酶A2突變體及其制備方法,ZL201410279966.3.[5] 路福平,劉逸寒,張濤,劉曉光,王正祥,王春霞,王建玲.sn-2位為二十二碳六烯酸的磷脂酰絲氨酸的制備方法,ZL201410279967.8.[6] 路福平,劉逸寒,劉敏堯,劉靚,樊帥,王春霞,王建玲.堿性蛋白酶高產(chǎn)菌株及其所產(chǎn)的堿性蛋白酶,ZL201210417021.4.[7] 路福平,劉逸寒,鄭宏臣,樊帥,王春霞 王建玲.一種耐高溫高堿木聚糖酶及其基因工程菌和制備方法,ZL201210470064.9.[8] 路福平,劉逸寒,藺松,王春霞,王建玲.一種抑制枯草芽孢桿菌谷氨酰胺轉(zhuǎn)胺酶活性的多肽及其篩選方法和應(yīng)用,ZL201210585268.7.[9] 路福平,劉逸寒,鄭宏臣,王春霞,王建玲.一種耐高溫木聚糖酶的高產(chǎn)菌株及利用該菌發(fā)酵產(chǎn)耐高溫木聚糖酶的方法及得到的酶,ZL201110282029.X.[10] 李玉,荊瑋,劉逸寒,劉曉光,王穩(wěn)航,路福平.一種β-葡萄糖苷酶產(chǎn)生菌及利用該菌轉(zhuǎn)化制備京尼平的方法,ZL201110243864.2.[11] 路福平,劉逸寒,劉敏堯,劉靚,薄嘉鑫,王春霞,王建玲.一種低溫堿性蛋白酶及其制備方法,ZL201110220386.3.[12] 路福平,劉逸寒,薄嘉鑫,王春霞,王建玲.高活力磷脂酶D及細(xì)胞表面展示磷脂酶D酵母全細(xì)胞催化劑的制備,ZL201110206481.8.[13] 路福平,郝育杰,劉逸寒,王春霞,肖靜,周浩,蔣彥潔,王珊.一種堿性果膠酶基因工程菌培養(yǎng)條件的優(yōu)化方法,ZL200910070737.X[14] 路福平,杜連祥,劉逸寒,李玉,王建玲,王春霞.高溫耐酸性α-淀粉酶的突變株及其構(gòu)建方法,ZL200810053625.9.[15] 路福平,杜連祥,李濤,史文玉,劉逸寒.采用無機(jī)膜實(shí)現(xiàn)微生物原位分離發(fā)酵的方法,ZL200610015378.4.獲獎(jiǎng)情況[1] 一種耐酸性高溫α-淀粉酶及其基因工程菌和制備方法.2017年度天津市專利獎(jiǎng)金獎(jiǎng),排名第1.[2] 新型半纖維素酶創(chuàng)制關(guān)鍵技術(shù)的開發(fā)與應(yīng)用.2016年度中國輕工業(yè)聯(lián)合會(huì)科學(xué)技術(shù)進(jìn)步獎(jiǎng)二等獎(jiǎng),排名第1.[3] 耐高溫α-淀粉酶的定向進(jìn)化及其耐酸突變體在枯草芽孢桿菌中的表達(dá).2013年度天津市優(yōu)秀博士學(xué)位論文.[4] 重大淀粉酶品的創(chuàng)制綠色制造及其應(yīng)用.2013年度國家技術(shù)發(fā)明獎(jiǎng)二等獎(jiǎng),排名第6.[5] 一種耐高溫高堿木聚糖酶及其基因工程菌和制備方法.2016年度天津市專利獎(jiǎng)優(yōu)秀獎(jiǎng),排名第2.[6] 高溫耐酸性α-淀粉酶的突變株及其構(gòu)建方法.2015年度天津市專利獎(jiǎng)優(yōu)秀獎(jiǎng),排名第3.[7] 果醋釀造的關(guān)鍵技術(shù)及產(chǎn)業(yè)化.2014年度中國商業(yè)聯(lián)合會(huì)全國商業(yè)科技進(jìn)步獎(jiǎng),排名第5.[8] 高產(chǎn)脂肪酶菌株的選育及發(fā)酵工藝優(yōu)化.2014年度臨沂市科技進(jìn)步獎(jiǎng)二等獎(jiǎng),排名第2.

[科研工作]
以第一作者先后發(fā)表各類科技論文30余篇,其中SCI收錄22篇EI收錄1篇,獲得國家授權(quán)發(fā)明專利15項(xiàng)。代表性學(xué)術(shù)論文:[1]Liu YH* Li MJ Huang L Gui S Jia LB Zheng D Fu Y Zhang YT Rui JQ Lu FP*. Cloning expression and characterisation of phospholipase B from Saccharomyces cerevisiaeand its application in the synthesis of l-alpha-glyceryl phosphorylcholine and peanut oil degumming[J]. Biotechnology & Biotechnological Equipment doi.org/10.1080/13102818.2018.1455536.[2]Liu YH* Liu H Huang L Gui S Zheng D Jia LB Fu Y Lu FP*. Improvement in thermostability of an alkaline lipase I fromPenicillium cyclopiumby directed evolution[J]. RSC Advances 2017 7:38538-38548.[3] Liu YH* Huang L Jia LB Gui S Fu Y Zheng D Guo W Lu FP*. Improvement of the acid stability of Bacillus licheniformisalpha amylase by site-directed mutagenesis[J]. Process Biochemistry 2017 58:174-180.[4]Liu YH Huang L Guo W Jia LB Fu Y Gui S Lu FP*. Cloning expression and characterization of a thermostable and pH-stable laccase fromKlebsiella pneumoniaeand its application to dye decolorization[J]. Process Biochemistry 2017 53:125-134.[5] Liu YH Huang L Li MJ Liu H Guo W Gui S Niu JL Lu FP*. Characterization of the recombinant porcine pancreas phospholipase A2expressed in Pichia pastorisGS115 and its application to synthesis of 2-DHA-PS[J]. Process Biochemistry 2016 51(10):1472-1478.[6] Huang L1 Liu YH1 Liu XG Ban LT Wang Y Liu MJ Lu FP*. Functional expression of Trametes versicolor thermotolerant laccase variant in Pichia pastoris[J]. Biotechnology & Biotechnological Equipment 2016 30(2):261-269. (Co-first author)[7] Liu YH Huang L Liu WG Guo W Zheng HC WangJL Lu FP*. Studies on properties of the xylanbinding domain and linker sequence of xylanase XynG1-1 from Paenibacillus campinasensisG1-1[J]. Journal of Industrial Microbiology & Biotechnology 2015 42(12):1591-1599.[8]Liu YH Zhang T Qiao J Liu XG Bo JX Wang JL Lu FP*. High-yield phosphatidylserine production via yeast surface display of phospholipase D from Streptomyces chromofuscuson Pichia pastoris[J]. Journal of Agricultural and Food Chemistry 2014 62(23):5354-5360.[9]Liu YH Lin S Zhang XQ Liu XG Wang JL Lu FP*. A novel approach for improving the yield of Bacillus subtilistransglutaminase in heterologous strains[J]. Journal of Industrial Microbiology & Biotechnology 2014 41(8):1227-1235.[10]Liu YH Zhang T Zhang ZM Sun TY Wang JL Lu FP*. Improvement of cold adaptation of Bacillus alcalophilusalkaline protease by directed evolution[J]. Journal of Molecular Catalysis B: Enzymatic 2014 106:117-123.[11]Liu YH Fan S Liu XG Zhang ZM Wang JL Wang ZX* Lu FP*. A highly active alpha amylase from Bacillus licheniformis: directed evolution enzyme characterization and structural analysis[J]. Journal of Microbiology and Biotechnology 2014 24(7):898-904.[12]Liu YH Lin S Liu K Liu XG Zhang XQ Wang HB Lu FP*. High-level expression of the Streptomyces mobaraenseCICC11018 transglutaminase in Corynebacterium glutamicum ATCC13032[J]. Applied Biochemistry and Microbiology 2014 50(5):456-462.[13]Zheng HC1 Liu YH1 Sun MZ Han Y Wang JL Sun JS Lu FP*. Improvement of alkali stability and thermostability of Paenibacillus campinasensisFamily-11 xylanase by directed evolution and site-directed mutagenesis[J]. Journal of Industrial Microbiology & Biotechnology 2014 41(1):153-162. (Co-first author)[14]Wang YP1 Liu YH1 Wang ZX Lu FP*. Influence of promoter and signal peptide on the expression of pullulanase in Bacillus subtilis[J]. Biotechnology Letters 2014 36(9):1783-1789. (Co-first author)[15]Zhang Y1 Liu YH1 Li Y Liu XG Lu FP*. Extracellular expression of pullulanase from Bacillus naganoensisin Escherichia coli[J]. Annals of Microbiology 2013 63(1):289-294. (Co-first author)[16]Liu YH Hu B Xu YJ Bo JX Fan S Wang JL Lu FP*. Improvement of the acid stability of Bacillus licheniformisalpha amylase by error-prone PCR[J]. Journal of Applied Microbiology 2012 113(3):541-549.[17]Liu YH Chen GQ Wang JL Hao YJ Li M Li Y Hu B Lu FP*. Efficient expression of an alkaline pectate lyase gene from Bacillus subtilisand the characterization of the recombinant protein[J]. Biotechnology Letters 2012 34(1):109-115.[18]Zheng HC1 Liu YH1 Liu XG Han Y Wang JL Lu FP*. Overexpression of a Paenibacillus campinasensisxylanase in Bacillus megateriumand its applications to biobleaching of cotton stalk pulp and saccharification of recycled paper sludge[J]. Bioresource Technology 2012 125:182-187. (Co-first author)[19]Zheng HC1 Liu YH1 Liu XG Wang JL Han Y Lu FP*. Isolation purification and characterization of a thermostable Xylanase from a novel Strain Paenibacillus campinasensis G1-1[J]. Journal of Microbiology and Biotechnology 2012 22(7):930-938. (Co-first author)[20]Liu YH Lu FP* Chen GQ Snyder CL Sun J Li Y Wang JL Xiao J. High-level expression purification and characterization of a recombinant medium-temperature α-amylase from Bacillus subtilis[J]. Biotechnology Letters 2010 32(1):119-124.[21]Liu YH Lu FP* Li Y Yin XB Wang Y Gao C. Characterisation of mutagenised acid-resistant alpha-amylase expressed in Bacillus subtilisWB600[J]. Applied microbiology and biotechnology 2008 78(1):85-94. [22]Liu YH Lu FP* Li Y Wang JL Gao C. Acid stabilization of Bacillus licheniformisalpha amylase through introduction of mutations[J]. Applied microbiology and biotechnology 2008 80(5):795-803.[23]Liu YH Xu YJ Fan S BO JX Wang JL Lu FP*. Study on the influencing conditions in the electro-transformation efficiency of Bacillus licheniformisATCC14580[J]. Lecture Notes in Electrical Engineering 2014 251(3):1845-1853.

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