软起动器的数字控制技术

首先提出了全数字电子软起动器的优势和应用特点,接着描述了软起动器的硬件组成—主回路、检测回路、显示模块、数字控制器,并且简单的介绍了它们在电路中的功能和作用。重点介绍了软件设计中的关键部分—斜坡电压控制算法、限流起动算法和六个晶闸管的顺序触发算法在Intel80C196KC单片机的实现,其中限流起动是用传统的控制方法PID来实现。     

高核酸高蛋白酵母选育及发酵生态学研究

通过紫外线嘧啶复合处理选育到一株高核酸高蛋白酵母，并进行了营子及其它培养条件的选择性试验，确定了优化的培养条件，摇瓶培养核酸１４．７５％，蛋白质含量达６３．６７％。１．５Ｌ发酵罐发酵试验能很好地重现摇瓶效果及冰箱保存活试验证明该菌株有好的遗传稳定性。     

磁控式异步电动机软起动器的开发与应用

详细介绍了将传统磁放大器用于异步电机降压起动、实现软起动功能的原理以及实际实现线路，是异步电机减压软起动技术领域的一项创新。     

起动用铅酸蓄电池试验需注意的几个问题

本文主要讨论了起动用铅酸蓄电池试验时的几个注意点以及对检验结果造成的影响。     

利用果胶粕生产固体发酵饲料

用黑曲霉和酵母将果胶粕（生产果胶的废渣）进行固体发酵,确定了合适的氮源,水分、ｐＨ、时间等发酵条件,生产出蛋白含量较高的饲料。     

重组肠激酶在甲醇酵母中高效表达的培养条件研究

对重组肠激酶在甲醇酵母中高效表达的发酵条件进行了优化，并在BiofloⅢ发酵罐中实现了高密度培养和高效表达。结果表明；温度30C，培养基pH6．0，当酵母密度达到200A600mm以上时，加入无水甲醇，控制甲醇的流加体积，使其终体积分数为1．0％～3．O％，继续诱导培养72h左右，酵母菌密度可达到150g／L，重组肠激酶总活性可达58kIU／L发酵液。     

Inhibitory effect of the adenovirus type 5 E1A protein expressed in the yeast system

The human adenovirus type 5 E1A, a tumor- suppressor gene[1], codes for two major related proteins of 243 amino acids (12S) and 289 amino acids (13S) by al-ternative splicing in two exons[2]. Studies have been shown that E1A can regulate expression of many genes and cell cycle[3]. Both in vitro and in vivo experiments indicated that E1A could induce tumor cells differentia-tion, convert tumor cells into an epithelial phenotype, in-hibit tumor cell growth and metastasis and strongly en-ha…     

Inhibitory effect of the adenovirus type 5 E1A protein expressed in the yeast system of the human tumor cell growth

Adenovirus 5 type E1A as a tumor suppressor gene can inhibit tumor growth and enhance the censitivity of chemotherapy and radiotherapy.E1A have the ability to integrate into the host genome,resulting in long-time expres-sion that induces Rb gene inactivation and animal cells im-mortalization.This prompted us to select the E1A protein for treatment of cancer in order to overcome the limitations of E1A gene therapy.Thus,we firstly comstructed E1A eu-caryotic expression vector (pPIC9/E1A),transformated the pichia pastoris yeast cells(GS115) and screened the high-expressing recombinant strains.The positive yeast strains were cultured in the shake flask,and induced for 3d.The crude E1A protein was purified using two steps of col-umu chromatography on HiTrap Q and HiTrap SP.The pu-rified E1A protein was identified by SDS-PAGE and Western blot.E1A protein was mostly located at cellular unclear when Cheriot delivered E1A protein into cells.The analysis in vitro indicated that the E1A protein arrested LN686 cell cycle at G2/M phase,and significantly inhibited the growth of LN686 tumor cells.The current studies firstly provided an experimental basis to further develop E1A protein for tumor treatment.     

番茄早疫病拮抗菌酵母的筛选

从几种果实表面附生微生物群中分离到120株酵母菌.通过平板筛选法(invitro),筛选出11株酵母菌对番茄早疫病(Alternariasolani)有拮抗作用.等体积混菌试验表明,11株酵母菌中有7株酵母菌,浓度为106、107和108CFU·ml-1时,能完全抑制105、104、103spores·ml-13种浓度的交链孢霉生长.通过果实接种试验法(invi vo)发现,酵母菌菌株L-1-6能够高度抑制3个品种番茄早疫病的发生,平均抑制率达到77.8%.     

饵料及日采收率对蒙古裸腹溞培养效果的影响

~~饵料及日采收率对蒙古裸腹溞培养效果的影响@史海东$浙江海洋学院海洋与渔业研究所,浙江省海洋水产研究所!浙江舟山316100 @辛俭$浙江海洋学院海洋与渔业研究所,浙江省海洋水产研究所!浙江舟山316100 @王海岳$岱山县岱西镇人民政府!浙江岱山316200 @毛国民$浙江海洋学院海洋与渔业研究所,浙江省海洋水产研究所!浙江舟山316100 @姚海富$浙江海洋学院海洋与渔业研究所,浙江省海洋水产研究所!浙江舟山316100~~~~~~浙江省科技厅科研计划项目(021102111)…