何永兴-凯发k8官方网娱乐官方

凯发k8官方网娱乐官方的联系方式

  • 职  称: 教授
  • 所在部门: 生物物理所
  •  办公室: 天演楼217
  • 联系电话: 0931-8912563
  • 传真号码:
  • 电子邮件: [email protected]
  • 个人凯发k8官方网娱乐官方主页:
学习经历

2011/02-2013/02,加州大学伯克利分校,生物化学与分子生物学系(定量生物学研究所qb3),博士后

2005/09-2010/12,中国科大,生化与分子生物系,博士

2001/09-2005/07,中国科大,生命科学院,学士

 

工作经历

2013/03-2020/12,兰州大学生命科学学院,副教授

2020/12-至今, 兰州大学生命科学学院,教授

社会工作
研究方向

实验室主要致力于研究农业微生物次生代谢物合成的调控机制和对环境的适应性机制。目前已建立较为成熟的蛋白质组学和结构生物学平台,欢迎对生物信息学、蛋白质组学及微生物学感兴趣的同学报考本实验室研究生!

项目成果

国家自然科学基金委面上项目:吲哚调节荧光假单胞菌耐药性及莫匹罗星合成的分子机制研究(31971422),执行时间:2020/01-2023/12

国家自然科学基金委面上项目:毒素-抗毒素mqsra调控荧光假单胞菌抗药性的分子机制研究(31972319),执行时间:2020/01-2023/12

国家自然科学基金委面上项目:植物根际促生菌pseudomonas-fluorescems 2p24感受与影响类黄酮的分子机制研究,执行时间:2018/01-2021/12

国家自然科学基金委青年项目:荧光假单胞杆菌中的抗生素dapg合成酶的晶体结构及其催化机理,2014/01-2016/12

甘肃省自然科学基金面上项目:黄酮类物质对雄激素受体信号转导的拮抗机制研究,2019年/01-2020/12

国家自然科学基金委面上项目:2,4-dapg及mapg作为荧光假单胞菌信号分子的作用机制,执行时间:2020/01-2023/12 承担经费:22万

荣誉、获奖

2019年甘肃医学科技奖一等奖,排名5/9

2019年甘肃省科技进步二等奖,排名7/10

教学及指导研究生情况

讲授《生物信息学》《蛋白质组学》《结构生物学》等

 

发表论文及专著

发表论文(#通讯作者):

li dy, han jt, zhang my, yan x, zhang n, ge h, wang z#, he yx#. the two-component system rsta/rstb regulates expression of multiple efflux pumps and influences anaerobic nitrate respiration in pseudomonas fluorescens. msystems. 2021 nov 2;6(6):e0091121

feng y, lu y, li j, zhang h, li z, feng h, deng x, liu d, shi t, jiang w, he yx#, zhang j#, wang z#. design, synthesis and biological evaluation of novel o-aminobenzamide derivatives as potential anti-gastric cancer agents in vitro and in vivo. eur j med chem. 2022 jan 5;227:113888

song y*, zhang sp*, luo g, shen y, li c, zhu y, huang q, mou x, tang x, liu t, wu s, tong a, he yx#, bao r#. type ii antitoxin higa is a key virulence regulator in pseudomonas aeruginosa. acs infect dis. 2021 oct 8;7(10):2930-2940

han jt, zhu y, pan db, xue hx, wang s, peng y, liu h#, he yx#, yao x#. discovery of pentapeptide-inhibitor hits targeting fkbp51 by combining computational modeling and x-ray crystallography. comput struct biotechnol j. 2021 jul 21;19:4079-4091

zhang sp, feng hz, et al. feng hy#, he yx# proteomic analysis reveals the mechanism of different environmental stress -induced tolerance of pseudomonas aeruginosa pao1 to monochloramine disinfection. j hazard mater. 2021 sep 5;417:126082.

han jt, li dy, zhang my, yu xq, jia xx, xu h, yan x, jia wj, niu s, kempher ml, tao x, he yx#. emhr is an indole-sensing transcriptional regulator responsible for the indole-induced antibiotic tolerance in pseudomonas fluorescens. environ microbiol. 2021 apr;23(4):2054-2069

li t*, song y*, et al. he yx, bao r. molecular basis of the versatile regulatory mechanism of htra-type protease algw from pseudomonas aeruginosa. mbio. 2021 feb 23;12(1):e03299-20. 

song y, luo g, zhu y, li t, li c, he l, zhao n, zhao c, yang j, huang q, mu x, tang x, kang m, wu s, he yx#, bao r#. pseudomonas aeruginosa antitoxin higa functions as a diverse regulatory factor by recognizing specific pseudopalindromic dna motifs. environ microbiol. 2021 mar;23(3):1541-1558

zhang sp, feng hz, wang q, kempher ml, quan sw, tao x, niu s, wang y, feng hy#, he yx#. bacterial type ii toxin-antitoxin systems acting through post-translational modifications. comput struct biotechnol j. 2020 dec 11;19:86-93. 

guo dd*, luo lm* et al. he yx# the regulator pltz regulates a novel antibiotic efflux pump pltijknop of pseudomonas aeruginosa atcc 27853 in response to the antimicrobial 2,4-diacetylphloroglucinol. front microbiol. 2020 jul 8;11:1423

yu xq*, yan x*. et al. he yx# flavonoids repress production of antifungal 2,4-dapg but potentially facilitate root colonization of the rhizobacterium pseudomonas fluorescens. environ microbiol. 2020 dec;22(12):5073-5089

zhang sp, wang q, quan sw, yu xq, wang y, guo dd, peng l, feng hy#, he yx# type ii toxin-antitoxin system in bacteria: activation, function and mode of action. biophysical reports. 2020

na m, zhang s, liu j, ma s, han y, wang y, he yx, chen h, chen x. determination of pathogenic bacteria-bacillus anthrax spores in environmental samples by ratiometric fluorescence and test paper based on dual-emission fluorescent silicon nanoparticles. j hazard mater. 2020 mar 15;386:121956

zhang zy, bai hh, guo z, li hl, he yt, duan xl, suo zw, yang x, he yx, hu xd. mglur5/erk signaling regulated the phosphorylation and function of glycine receptor α1ins subunit in spinal dorsal horn of mice. plos biol. 2019 aug 21;17(8)

han jt*, zhang sp*, jia wj, zhang z, wang y, he yx#. discovery and structural analysis of a phloretin hydrolase from the opportunistic human pathogen mycobacterium abscessus. febs journal. 2019 

wang y*, zhang sp*, zhang my, kempher ml, guo dd, han jt, tao x, wu y, zhang lq, he yx#. the antitoxin mqsa homolog in pseudomonas fluorescens 2p24 has a rewired regulatory circuit through evolution. environ microbiol. 2019 

zhao jh, chen jh, wang y, wang zp#, he yx#. the putative compatible solute-binding protein prox from mycobacterium tuberculosis h37rv: biochemical characterization and crystallographic data. acta crystallogr f struct biol commun. 2018 apr 1;74(pt 4):231-235.

yan x, yang r, zhao rx, han jt, jia wj, li dy, wang y, zhang n, wu y, zhang lq#, he yx#. the transcriptional regulator phlh modulates 2,4-diacetylphloroglucinol biosynthesis in response to the biosynthetic intermediate and end product. appl environ microbiol. 2017 aug 18

li l, zhu y, zhou s, an x, zhang y, bai q, he yx#, liu h#, yao xj#. experimental and theoretical insights into the inhibition mechanism of prion fibrillation by resveratrol and its derivatives. acs chem neurosci. 2017 aug 17

sun c, yan k, han jt, tao l, lv mh, shi t, he yx, wierzba m, tax fe, li j.scanning for new bri1 mutations via tilling analysis. plant physiol. 2017 jul;174(3):1881-1896.

nan q, qian d, niu y, he yx, tong s, niu z, ma j, yang y, an l, wan d, xiang y. plant actin-depolymerizing factors possess opposing biochemical properties arising from key amino acid changes throughout evolution. plant cell. 2017 jan 25

wu d, tao x, chen zp, han jt, jia wj, zhu n, li x, wang zp#, he yx#the environmental endocrine disruptor p-nitrophenol interacts with fkbp51, a positive regulator of androgen receptor and inhibits androgen receptor signaling in human cells. j hazard mater. 2016 apr 15;307:193-201

 

 

 

其它信息

欢迎对蛋白质组学、微生物学及合成生物学感兴趣的同学报考本实验室研究生!

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