%0 Journal Article
%T Construction of copper-induced gene expression platform in Synechocystis sp. PCC6803<br>集胞藻PCC6803铜离子诱导表达平台的构建
%A GAO Hong
%A TANG Qing
%A XU Xu-Dong
%A <br>高宏
%A 唐蜻
%A 徐旭东
%J 水生生物学报
%D 2007
%I 
%X In Synechocystis sp. PCC6803,gene knock-out is the most straightforward and effective method to reveal the physiological function of a gene.Nevertheless,insertion mutants could not be generated for those genes essential to survival.In order to elucidate the function of such genes in Synechocystis sp.PCC6803,a copper-induced gene expression platform was constructed using the promoter of petE(PpetE).PpetE from Synechocystis sp.PCC6803 and the beta-galactosidase gene(lacZ) from E.coli GM48 were cloned respectively by doing polymerase chain reaction(PCR),and the PpetE was positioned upstream of lacZ.The PpetE-lacZ construct was integrated into the genome of Synechocystis sp.PCC6803 via homologous recombinations.The expression of beta-galactosidase gene was found to be controllable by adjusting the concentration of Cu2+ in medium. In a range from 6 to 400nmol/L,Cu2+ induced the expression of beta-galactosidase in an S-shaped curve,but when the concentration of Cu2+ in medium was below 6nmol/L or above 400nmol/L,the activity of beta-galactosidase was either too low to be detected or too high to be regulated.This copper-induced gene expression platform can be used in the control of some indispensable genes in Synechocystis sp.PCC6803: cells survived in the presence of Cu2+,so that the physiological effect of a gene could be observed when Cu2+ is removed.
%K PpetE
%K lacZ<br>集胞藻
%K 铜离子
%U http://www.alljournals.cn/get_abstract_url.aspx?pcid=90BA3D13E7F3BC869AC96FB3DA594E3FE34FBF7B8BC0E591&jid=256651267D5D2E4520A7707D05E98747&aid=257033980792ED7E&yid=A732AF04DDA03BB3&vid=59906B3B2830C2C5&iid=0B39A22176CE99FB&sid=CA4FD0336C81A37A&eid=5B5B75F4854B8331&journal_id=1000-3207&journal_name=水生生物学报&referenced_num=0&reference_num=12