Design and characterization of molecular tools for a Synthetic Biology approach towards developing cyanobacterial biotechnology

被引:248
作者
Huang, Hsin-Ho [1 ]
Camsund, Daniel [1 ]
Lindblad, Peter [1 ]
Heidorn, Thorsten [1 ]
机构
[1] Uppsala Univ, Dept Photochemistry & Mol Sci, Angstrom Labs, SE-75120 Uppsala, Sweden
关键词
GREEN FLUORESCENT PROTEIN; CAMP RECEPTOR PROTEIN; SYNECHOCYSTIS SP PCC-6803; BROAD-HOST-RANGE; HIGH COPY NUMBER; GENE-EXPRESSION; PROMOTER RECOGNITION; CONJUGAL TRANSFER; ESCHERICHIA-COLI; RESISTANCE GENES;
D O I
10.1093/nar/gkq164
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cyanobacteria are suitable for sustainable, solar-powered biotechnological applications. Synthetic biology connects biology with computational design and an engineering perspective, but requires efficient tools and information about the function of biological parts and systems. To enable the development of cyanobacterial Synthetic Biology, several molecular tools were developed and characterized: (i) a broad-host-range BioBrick shuttle vector, pPMQAK1, was constructed and confirmed to replicate in Escherichia coli and three different cyanobacterial strains. (ii) The fluorescent proteins Cerulean, GFPmut3B and EYFP have been demonstrated to work as reporter proteins in cyanobacteria, in spite of the strong background of photosynthetic pigments. (iii) Several promoters, like P-rnpB and variants of P-rbcL, and a version of the promoter P-trc with two operators for enhanced repression, were developed and characterized in Synechocystis sp. strain PCC6803. (iv) It was shown that a system for targeted protein degradation, which is needed to enable dynamic expression studies, is working in Synechocystis sp. strain PCC6803. The pPMQAK1 shuttle vector allows the use of the growing numbers of BioBrick parts in many prokaryotes, and the other tools herein implemented facilitate the development of new parts and systems in cyanobacteria.
引用
收藏
页码:2577 / 2593
页数:17
相关论文
共 74 条
[1]   Redox control of ntcA gene expression in Synechocystis sp PCC 6803.: Nitrogen availability and electron transport regulate the levels of the NtcA protein [J].
Alfonso, M ;
Perewoska, I ;
Kirilovsky, D .
PLANT PHYSIOLOGY, 2001, 125 (02) :969-981
[2]   Redox control of psbA gene expression in the cyanobacterium Synechocystis PCC 6803.: Involvement of the cytochrome b6/f complex [J].
Alfonso, M ;
Perewoska, I ;
Kirilovsky, D .
PLANT PHYSIOLOGY, 2000, 122 (02) :505-515
[3]   CONSTRUCTION OF A SYNECHOCYSTIS PCC6803 MUTANT SUITABLE FOR THE STUDY OF VARIANT HEXADECAMERIC RIBULOSE-BISPHOSPHATE CARBOXYLASE OXYGENASE ENZYMES [J].
AMICHAY, D ;
LEVITZ, R ;
GUREVITZ, M .
PLANT MOLECULAR BIOLOGY, 1993, 23 (03) :465-476
[4]  
Andersen JB, 1998, APPL ENVIRON MICROB, V64, P2240
[5]   SPECIFIC-PURPOSE PLASMID CLONING VECTORS .2. BROAD HOST RANGE, HIGH COPY NUMBER, RSF1010-DERIVED VECTORS, AND A HOST-VECTOR SYSTEM FOR GENE CLONING IN PSEUDOMONAS [J].
BAGDASARIAN, M ;
LURZ, R ;
RUCKERT, B ;
FRANKLIN, FCH ;
BAGDASARIAN, MM ;
FREY, J ;
TIMMIS, KN .
GENE, 1981, 16 (1-3) :237-247
[6]   Interactions of CcdB with DNA gyrase - Inactivation of GyrA, poisoning of the gyrase-DNA complex, and the antidote action of CcdA [J].
Bahassi, EM ;
O'Dea, MH ;
Allali, N ;
Messens, J ;
Gellert, M ;
Couturier, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (16) :10936-10944
[7]  
Becker E., 1997, J. Bacteriol, V179, P5947, DOI [DOI 10.1128/JB.179.18.5947-5950.1997, 10.1128/jb.179.18.5947-5950.1997]
[8]   A COMPLEMENTATION ANALYSIS OF RESTRICTION AND MODIFICATION OF DNA IN ESCHERICHIA COLI [J].
BOYER, HW ;
ROULLAND.D .
JOURNAL OF MOLECULAR BIOLOGY, 1969, 41 (03) :459-&
[9]  
BROSIUS J, 1985, J BIOL CHEM, V260, P3539
[10]   Transcription activation by catabolite activator protein (CAP) [J].
Busby, S ;
Ebright, RH .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 293 (02) :199-213