In this work, the functions of promoter fragments of two potential salt-tolerance related genes of Spirulina (Spirulina platensis Geitl.) were studied using green fluorescent protein gene (gfp) as a reporter. The promoter structures of two salt-tolerance related genes of Spirulina were predicted using online promoter prediction software. pMD18-T and pUC18 vectors were used to clone the promoter sequences as well as the gfp gene and kanamycine resistance (kan) gene. The fragments containing pro-gfp-kanr were further cloned into pKW1188 vector and the resulting recombinant plasmids were then transformed into a host strain Synechocystis sp. (Synechocystis pevalekii Ercegovic) PCC6803. The resulting bacterial strains were grown under various concentrations of salinity for defining time intervals. The bacterial fluorescence was observed using laser confocal microscope. Our results showed that the transgenic bacteria grown at different concentrations of salinity for various periods produced varying fluorescence intensities. The bacteria treated with NaCl at the concentrations of 0.4mol/L to 0.6mol/L for 6 to 8 h showed the strongest fluorescent intensity. From the result of high salt induced expression of gfp, we predicted that the genes under control of these two promoters are likely to play important roles in the salt tolerance of Spirulina. Accordingly, we believed that a research platform for the studying functions of the promoters of the salt-tolerance related genes in Spirulina has been developed with the gfp as a reporter, the kanr gene as the selection marker, and Synechocystis. sp. PCC6803 as the expression host.
LI Pan-Pan, YONG Jing-Ru, JI Yun-Ling, ZHANG Ying, DIAO Liang, JIA Shi-Lin, LI Dong, WANG Hui-Li, BAO Ji-Yu, LI Pei-Zhen
. Functional analysis of promoter fragments of salt-tolerance related genes in Spirulina[J]. Hereditas(Beijing), 2011
, 33(10)
: 1134
-1140
.
DOI: 10.3724/SP.J.1005.2011.01134
[1] Thomas DJ, Sullivan SL, Price AL, Zimmerman SM. Common freshwater cyan bacteria grow in 100% CO2. Astrobiology, 2005, 5(1): 66-74.
[2] Ayachi S, El Abed A, Dhifi W, Marzouk B. Chlorophylls, proteins and fatty acids amounts of arthrospira platensis growing under saline conditions. Pak J Biol Sci, 2007, 10(14): 2286-2291.
[3] Wiangnon K, Raksajit W, Incharoensakdi A. Presence of a Na+-stimulated P-type ATPase in the plasma membrane of the alkaliphilic halotolerant cyano-bacterium Aphanothece halophytica. FEMS Microbiol Lett, 2007, 270(1): 139-145.
[4] 方孝东, 林栖凤, 李冠一, 屈良鹄. 盐藻线粒体GIY-YIG族归巢内切酶基因受到盐胁迫时增强转录. 中国生物化学与分子生物学报, 2003, 10(5): 625-629.
[5] Fisher M, Gokhman I, Pick U, Zamir A. A structurally novel transferring-like protein accumulates in the plasma membrane of the unicellular green alga Dunaliella salina grown in high salinities. J Biol Chem, 1997, 272(3): 1565-1570.
[6] Fisher M, Zamir A, Pick U. Iron uptake by the halotolerant alga Dunaliella is mediated by a plasma membrane transferrin. J Biol Chem, 1998, 273(28): 17553-17558.
[7] Http://www.kazusa.or.jp/cyanobase/synechocystis/index.html.
[8] 毛云翔, 张宝红, 杨官品, 张学成. 节旋藻 (螺旋藻) 高分子量DNA的两种制备方法. 海洋科学, 2003, 27(2): 32-36.
[9] 徐旭东, 王业勤, 黎尚豪. 鱼腥藻-大肠杆菌启动子CAT探测载体的构建. 中国科学院研究生院学报, 1993, 10(2): 203-209.
[10] 迪芬巴赫 CW, 德维克斯勒 GS. PCR实验技术指南. 黄培堂, 俞炜源, 陈添弥, 等译. 北京: 科学出版社, 1998: 380-415.
[11] McClure WR. Mechanism and control of transcription initiation in Prokaryotes. Ann Rev Biochem, 1985, 54: 171-204.
[12] Williams JGK. Construction of specific mutations in photosystem II photosynthetic reaction center by genetic engineering methods in Synechocystis 6803. Methods Enzymol, 1988, 167: 766-778.
[13] Hautefort I, Proença MJ, Hinton JCD. Single-copy green fluorescent protein gene fusions allow accurate measurement of Salmonella gene expression in vitro and during infection of mammalian cells. Appl Environ Microbiol, 2003, 69(12): 7480-7491.