J Biotechnol 146(3):120–125PubMedCrossRef Wu S, Xu L, Huang R, Wang Q (2011) Improved biohydrogen production with an expression of codon-optimized hemH and lba genes in the chloroplast of Chlamydomonas reinhardtii. Bioresour Technol 102:2610–2616PubMedCrossRef Xiong J, Subramaniam S, Govindjee (1998) A knowledge-based three dimensional model of the photosystem II reaction center of Chlamydomonas reinhardtii. Photosynth Res 56(3):229–254CrossRef Xu F, Ma W, Zhu X {Selleck Anti-diabetic Compound Library|Selleck Antidiabetic Compound Library|Selleck Anti-diabetic Compound Library|Selleck Antidiabetic Compound Library|Selleckchem Anti-diabetic Compound Library|Selleckchem Antidiabetic Compound Library|Selleckchem Anti-diabetic Compound Library|Selleckchem Antidiabetic Compound Library|Anti-diabetic Compound Library|Antidiabetic Compound Library|Anti-diabetic Compound Library|Antidiabetic Compound Library|Anti-diabetic Compound Library|Antidiabetic Compound Library|Anti-diabetic Compound Library|Antidiabetic Compound Library|Anti-diabetic Compound Library|Antidiabetic Compound Library|Anti-diabetic Compound Library|Antidiabetic Compound Library|Anti-diabetic Compound Library|Antidiabetic Compound Library|Anti-diabetic Compound Library|Antidiabetic Compound Library|Anti-diabetic Compound Library|Antidiabetic Compound Library|buy Anti-diabetic Compound Library|Anti-diabetic Compound Library ic50|Anti-diabetic Compound Library price|Anti-diabetic Compound Library cost|Anti-diabetic Compound Library solubility dmso|Anti-diabetic Compound Library purchase|Anti-diabetic Compound Library manufacturer|Anti-diabetic Compound Library research buy|Anti-diabetic Compound Library order|Anti-diabetic Compound Library mouse|Anti-diabetic Compound Library chemical structure|Anti-diabetic Compound Library mw|Anti-diabetic Compound Library molecular weight|Anti-diabetic Compound Library datasheet|Anti-diabetic Compound Library supplier|Anti-diabetic Compound Library in vitro|Anti-diabetic Compound Library cell line|Anti-diabetic Compound Library concentration|Anti-diabetic Compound Library nmr|Anti-diabetic Compound Library in vivo|Anti-diabetic Compound Library clinical trial|Anti-diabetic Compound Library cell assay|Anti-diabetic Compound Library screening|Anti-diabetic Compound Library high throughput|buy Antidiabetic Compound Library|Antidiabetic Compound Library ic50|Antidiabetic Compound Library price|Antidiabetic Compound Library cost|Antidiabetic Compound Library solubility dmso|Antidiabetic Compound Library purchase|Antidiabetic Compound Library manufacturer|Antidiabetic Compound Library research buy|Antidiabetic Compound Library order|Antidiabetic Compound Library chemical structure|Antidiabetic Compound Library datasheet|Antidiabetic Compound Library supplier|Antidiabetic Compound Library in vitro|Antidiabetic Compound Library cell line|Antidiabetic Compound Library concentration|Antidiabetic Compound Library clinical trial|Antidiabetic Compound Library cell assay|Antidiabetic Compound Library screening|Antidiabetic Compound Library high throughput|Anti-diabetic Compound high throughput screening| (2011) Introducing pyruvate oxidase into the chloroplast of Chlamydomonas reinhardtii increases

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and ferredoxin:NADP+-oxidoreductase (FNR) enzymes in vitro. Proc Natl Acad Sci USA 108(23):9396–9401PubMedCentralPubMedCrossRef”
“Introduction Algae are simple, photosynthetic, generally aquatic organisms that, like plants, use energy from sunlight to sequester carbon dioxide (CO2) from the atmosphere into biomass through BIX 1294 purchase photosynthesis. Plants evolved from ancient algae ancestors, and the photosynthetic machinery in both plants and algae originally came from the same source: cyanobacteria (Falcón et al. 2010; Fehling et al. 2007). Although algae and plants differ in many

ways, the fundamental processes, such as photosynthesis, that make them so distinguished among Earth’s organisms and this website valuable as crops, are the same. Certain strains of algae have been used for anthropogenic purposes for thousands of years, including as supplements and nutraceuticals (Kiple and Ornelas 2000) and in the fertilization of rice paddies (Tung and Shen 1985). As early as the 1940s, other strains were identified as possible fuel sources (Borowitzka 2013a) because of their ability to produce fuel or fuel precursor molecules. Large-scale production and cultivation systems, including photobioreactors and outdoor open Bay 11-7085 ponds, were developed in the early 1950s in the U.S., Germany, Japan, and the Netherlands (Borowitzka 2013b; Tamiya 1957). By the onset of the U.S. Department of Energy’s (DOE) aquatic species program (ASP) in the U.S. in 1980, various species of microalgae and cyanobacteria were being produced and farmed on commercial scales around the world, and had been for over 20 years, mostly for the health food and nutritional supplement industries (Borowitzka 2013b). Microalgae have evolved to be practically ubiquitous throughout the globe, and their varied distributions and evolutionary histories (Fehling et al. 2007) are reflected in extremely diverse metabolic capabilities between species (Andersen 2013).