姬芳玲

Associate Professor   Supervisor of Doctorate Candidates   Supervisor of Master's Candidates

Gender:Female

Alma Mater:大连理工大学

Degree:Doctoral Degree

School/Department:生物工程学院

Discipline:Bioengineering

Business Address:生物工程学院547房间

E-Mail:fanglingji@dlut.edu.cn


Paper Publications

LotS/LotR/Clp, a novel signal pathway responding to temperature, modulating protease expression via c-di-GMP mediated manner in Stenotrophomonas maltophilia FF11

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Indexed by:期刊论文

Date of Publication:2018-01-01

Journal:MICROBIOLOGICAL RESEARCH

Included Journals:PubMed、SCIE

Volume:214

Page Number:60-73

ISSN No.:0944-5013

Key Words:Stenotrophomonas maltophilia; Protease; Clp; Two-component system; Signal pathway; Low temperature

Abstract:Stenotrophomonas maltophilia as one of increasing food spoilage bacteria and fish pathogens has become a threat to aquiculture industry. A major factor contributing to the success of bacterium is its outstanding ability to secrete protease at low temperatures. Here, a cAMP receptor like protein (Clp) shows a positive regulation on this protease, named S. maltophilia temperature-response protease (SmtP). Interestingly, a two-component system, comprising of LotS sensor and LotR regulator, for low-temperature response is also confirmed to modulate SmtP expression with similar effect to Clp. Evidence is presented that LotS/LotR modulates smtP (coding SmtP) expression via Clp: clp promoter activity was reduced significantly at low temperatures and protease activity was partially restored by Clp overexpressed in /otS or lotR deletion strain. Furthermore, as a Clp negative effector, the binding ability of c-di-GMP with Clp is not impacted by temperature. c-di-GMP level was increased in S. maltophilia growing at high temperature, but not exhibited significantly in lotR deleted strain, these indicate that LotR is required for temperature modulating c-di-GMP level, although the synthesis or degradation activity of c-di-GMP by LotR was not detected. These findings suggest that LotS/LotR/Clp play an important role in responding to temperature stimuli via c-di-GMP mediated manner.

Pre One:Studies on structure-function relationships of acetolactate decarboxylase from Enterobacter cloacae

Next One:Structural and enzymatic characterization of acetolactate decarboxylase from Bacillus subtilis.

Profile

诚邀有志于探索生命科学前沿的优秀学子,携手推动相关领域的科学研究与创新!

       本团队现面向对生物工程、生物医用材料、免疫学、生物信息学、生物学及医学研究等领域感兴趣、热爱科学研究的同学,招收硕士和博士研究生。

 

       姬芳玲,工学博士,副教授,博士生导师,国际磁共振学会会员,美国化学会ACS会员,中国生物材料学会血液净化材料分会委员。研究方向为重大疾病(自身免疫性疾病)发生发展机制、(纳米)抗体的结构与功能、淋巴细胞分离及细胞异质性研究。主持国家自然科学基金2项,省部级基金1项,参加国家重点项目1项。研究成果发表在Angew. Chem.Analytical ChemistryActa Biomaterialia Bioconjugate Chemistry等国际一流期刊。已授权中国发明专利3项。

       2006年本科毕业于大连理工大学,获生物工程工学学士学位。2013年研究生毕业于大连理工大学,获生物化工工学博士学位。攻读博士学位期间,获得国家留学基金委资助,前往美国匹兹堡大学医学部结构生物学系进行博士联合培养,联合培养博士导师美国国家科学院院士、英国皇家化学学会会士Angela M. Gronenborn 教授。2013年12月入职大连理工大学生命科学与技术学院。荣获2020年全国高校生命科学类微课教学比赛三等奖。辽宁省普通高等教育(本科)教学成果奖二等奖(排名第六)大连理工大学优秀教育教学成果一等奖(排名第六)。2022年入选辽宁省首届优秀研究生导师团队成员。主译并由高等教育出版社出版Damien Nevoltris和Patrick Chames编著的《抗体工程》(第三版)。指导本科生荣获全国大学生生命科学竞赛二等奖、指导“大学生创新创业训练计划”国家级、省级和校级等项目。

 

工作及教育经历

2022/12至今,大连理工大学,生物工程学院,博士生导师

2018/12至今,大连理工大学,生物工程学院,副教授

2013/12-2018/11,大连理工大学,生命科学与技术学院,讲师

2013/08-2013/11,大连理工大学,生命科学与技术学院,师资博士后

2010/09-2012/10,美国匹兹堡大学医学部结构生物学系,联合培养博士

2006/09-2013/07,大连理工大学,生物化工专业,博士学位(保研)

2002/09-2006/07,大连理工大学,生物工程专业,学士学位