中国蔬菜
中國蔬菜
중국소채
CHINA VEGETABLES
2014年
5期
11-18
,共8页
王巧丽%梁燕%张振才%李翠%李云洲%王玲慧
王巧麗%樑燕%張振纔%李翠%李雲洲%王玲慧
왕교려%량연%장진재%리취%리운주%왕령혜
番茄%类胡萝卜素%E8启动子%CaMV 35S启动子%GUS染色
番茄%類鬍蘿蔔素%E8啟動子%CaMV 35S啟動子%GUS染色
번가%류호라복소%E8계동자%CaMV 35S계동자%GUS염색
Cherry tomato%Carotenoid%E8 promoter%CaMV 35S promoter%GUS
为了研究番茄LYC-B干扰对类胡萝卜素合成主要酶和主要代谢产物的影响,构建了果实特异性的番茄红素β-环化酶LYC-B干扰载体,并验证了其在不同颜色番茄果实中的有效性。依据X13437.1扩增番茄果实特异启动子E8,构建了果实特异性载体E8-pBI121,其在粉色、红色、绿色和紫色的番茄果实中均能表达。依据X86452.1扩增番茄LYC-B从61~861 bp 间长度为801 bp的片段LYC-B1和从480~781 bp 间长度为302 bp的片段 LYC-B2,构建了以CaMV 35S为启动子的LYC-B干扰表达载体pBI121-B1B2,以E8替换CaMV 35S,构建了果实特异性干扰载体E8-pBI121-B1B2。采用农杆菌注射法分别侵染番茄叶片和果实,GUS染色显示,pBI121-B1B2在叶片、果实和种子中均表达,E8-pBI121-B1B2只在果实和种子中表达。
為瞭研究番茄LYC-B榦擾對類鬍蘿蔔素閤成主要酶和主要代謝產物的影響,構建瞭果實特異性的番茄紅素β-環化酶LYC-B榦擾載體,併驗證瞭其在不同顏色番茄果實中的有效性。依據X13437.1擴增番茄果實特異啟動子E8,構建瞭果實特異性載體E8-pBI121,其在粉色、紅色、綠色和紫色的番茄果實中均能錶達。依據X86452.1擴增番茄LYC-B從61~861 bp 間長度為801 bp的片段LYC-B1和從480~781 bp 間長度為302 bp的片段 LYC-B2,構建瞭以CaMV 35S為啟動子的LYC-B榦擾錶達載體pBI121-B1B2,以E8替換CaMV 35S,構建瞭果實特異性榦擾載體E8-pBI121-B1B2。採用農桿菌註射法分彆侵染番茄葉片和果實,GUS染色顯示,pBI121-B1B2在葉片、果實和種子中均錶達,E8-pBI121-B1B2隻在果實和種子中錶達。
위료연구번가LYC-B간우대류호라복소합성주요매화주요대사산물적영향,구건료과실특이성적번가홍소β-배화매LYC-B간우재체,병험증료기재불동안색번가과실중적유효성。의거X13437.1확증번가과실특이계동자E8,구건료과실특이성재체E8-pBI121,기재분색、홍색、록색화자색적번가과실중균능표체。의거X86452.1확증번가LYC-B종61~861 bp 간장도위801 bp적편단LYC-B1화종480~781 bp 간장도위302 bp적편단 LYC-B2,구건료이CaMV 35S위계동자적LYC-B간우표체재체pBI121-B1B2,이E8체환CaMV 35S,구건료과실특이성간우재체E8-pBI121-B1B2。채용농간균주사법분별침염번가협편화과실,GUS염색현시,pBI121-B1B2재협편、과실화충자중균표체,E8-pBI121-B1B2지재과실화충자중표체。
The experiment will be conducted to research the specific impacts of lycopene β-cyclase interference on carotenoid metabolism,cherry tomato(Solanum lycopersicum L. var. cerasiforme Alef.) fruit-specific lycopene β-cyclase interference vector was constructed,and the validity in different color fruits were verified. Cherry tomato fruit-specific promoter E8 was amplified according to X13437.1 and fruit-specific vector of E8-pBI121 was constructed,which could be expressed in cherry tomato fruits of pink,red,green and purple colors. According to X86452.1,two different lycopene β-cyclase sequences B1 and B2 were amplified,LYC-B1 with 801 bp from 61 bp to 861 bp and LYC-B2 with 302 bp from 480 bp to 781 bp of LYC-B. The interference vector of pBI121-B1B2 with CaMV 35S promotor and the fruit-specific expression interference vectors of E8- pBI121-B1B2 with E8 promotor were constructed. E8-pBI121,pBI121-B1B2 and E8-pBI121-B1B2 were transferred into Agrobacterium tumefaciens GV3101 with the freeze-thaw method,then transformed into living cherry tomato fruits and leaves by injection. The results of GUS staining 7 days after injection showed that E8-pBI121 expressed in pink,red,green and purple cherry tomato fruits;pBI121-B1B2 expressed in leaves,fruits and seeds,while E8- pBI121-B1B2 expressed just in fruits and seeds.