水稻早衰突变体LS-es1的基因定位及候选基因分析
周纯1,焦然1,胡萍2,林晗1,胡娟1,徐娜1,吴先美2,饶玉春1,*(
),王跃星2,*()
),王跃星2,*()
Gene Mapping and Candidate Gene Analysis of Rice Early Senescence Mutant LS-es1
Chun Zhou1,Ran Jiao1,Ping Hu2,Han Lin1,Juan Hu1,Na Xu1,Xianmei Wu2,Yuchun Rao1,*(),Yuexing Wang2,*()
),Yuexing Wang2,*()
图4. 抽穗期水稻突变体LS-es1及其野生型(WT)叶片的过氧化氢酶(CAT) (A)、过氧化物酶(POD) (B)和超氧化物歧化酶(SOD) (C)活性以及丙二醛(MDA) (D)和过氧化氢(H2O2) (E)含量
*和**分别表示TP309与LS-es1在0.05和0.01水平上差异显著。
Figure 4. Catalase (CAT) (A), peroxisome (POD) (B), and superoxide dismutase (SOD) (C) activities and malondialdehyde (MDA) (D) and H2O2 (E) contents of LS-es1 and wild type (WT) at heading stage of rice
* and ** indicate significant differences between TP309 and LS-es1 at 0.05 and 0.01 level, respectively.
