Effect of short term cold stress on rice seedlings

A method was developed for exposing riceseedlings to low temperatures for shortperiods. These seedlings were from 70F₉ inbred lines derived originallyfrom a hybrid of a salt tolerant cultivar,which provided a source of resistance toabiotic stress, and a non salt tolerantcultivar as the other parent. Seedlingswere grown hydroponically in a warm growthroom then placed in the air above afreezing bath for 6 hours at –0.2 ^°C,–1.0 ^°C or –2.0 ^°C beforereturning them to the growth room for a7–10 day period. Seedling survival in theinbred lines of rice was compared afterexposure to these temperature treatments toidentify the presence of low temperaturetolerance. An average survival of 93%occurred 7days after exposures to –0.2, and–1.0 ^°C and a survival of 35% afteran exposure of –2.0 ^°C. The non-salttolerant parent cultivar was killed byexposure to –2.0 ^°C but the salttolerant parent survived. The effect of lowtemperature exposure was examined in moredetail in lines selected for lowtemperature tolerance and susceptibility.Alterations to the total leaf proteinprofile, including fragmentation ofRubisco, were observed in these lines butno obvious difference was detected betweensusceptible and tolerant individuals.     

水稻Rubisco及其活化酶的免疫金标定位

采用免疫胶体金标记电镜技术对水稻叶片中的Rubisco及其活化酶进行细胞器定位,结果表明Rubisco主要分布于叶绿体,Rubisco活化酶特异性分布于叶绿体和线粒体中,预示Rubisco活化酶可能具有除活化钝化态Rubisco以外的其他功能.     

Isolation and characterization of the rbcS genes from a sterile mutant of Ulva pertusa (Ulvales,Chlorophyta) and transient gene expression using the rbcS gene promoter

We isolated two different genomic DNAs (UprbcS1 and UprbcS2) encoding the small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase and portions of the 5′- and 3′-flanking regions from sterile Ulva pertusa Kjellman. The UprbcS1 and UprbcS2 genes had three introns in the coding region. Each predicted UprbcS polypeptide was a 180-amino-acid (AA) residue including a 38-AA transit peptide, although the 104th AA residue was replaced. The nucleotide sequences of UprbcS cDNAs isolated from a cDNA library corresponded to that of the UprbcS1 gene, suggesting that the UprbcS1 gene was predominantly expressed in sterile U. pertusa compared to UprbcS2. Southern blot analysis showed that each UprbcS gene was a single-copy gene in the sterile U. pertusa genome. Northern hybridization indicated that the expression of UprbcS was induced and repressed by dark and light treatments, respectively. When sterile U. pertusa cells were transformed with an expression vector containing the UprbcS1 promoter and terminator sequences fused with the green fluorescent protein (GFP) gene, GFP fluorescence was observed in the cells transformed. These results suggest that the UprbcS1 gene promoter is light regulated and highly active in the sterile U. pertusa cells and is available for genetic transformation system in the alga.