Utilization and characterization of photosynthetic bacteria rhodobacter sphaeroides for bioelectricity generation

2015 ◽  
Author(s):  
Man Tung Wong
1991 ◽  
Vol 7 (Supple) ◽  
pp. 821-824
Author(s):  
SUNAO YAMAZAKI ◽  
NAOYUKI KOBAYASHI ◽  
AKIRA OKUBO ◽  
TOSHIO SATO ◽  
YUZURU TOZAWA ◽  
...  

2021 ◽  
Vol 20 (1) ◽  
Author(s):  
Xiaomin Wu ◽  
Guang Ma ◽  
Chuanyang Liu ◽  
Xin-yuan Qiu ◽  
Lu Min ◽  
...  

Abstract Background Pinene is a monoterpene, that is used in the manufacture of fragrances, insecticide, fine chemicals, and renewable fuels. Production of pinene by metabolic-engineered microorganisms is a sustainable method. Purple non-sulfur photosynthetic bacteria belong to photosynthetic chassis that are widely used to synthesize natural chemicals. To date, researches on the synthesis of pinene by purple non-sulfur photosynthetic bacteria has not been reported, leaving the potential of purple non-sulfur photosynthetic bacteria synthesizing pinene unexplored. Results Rhodobacter sphaeroides strain was applied as a model and engineered to express the fusion protein of heterologous geranyl diphosphate synthase (GPPS) and pinene synthase (PS), hence achieving pinene production. The reaction condition of pinene production was optimized and 97.51 μg/L of pinene was yielded. Then, genes of 1-deoxy-d-xylulose 5-phosphate synthase, 1-deoxy-d-xylulose 5-phosphate reductoisomerase and isopentenyl diphosphate isomerase were overexpressed, and the ribosome binding site of GPPS-PS mRNA was optimized, improving pinene titer to 539.84 μg/L. Conclusions In this paper, through heterologous expression of GPPS-PS, pinene was successfully produced in R. sphaeroides, and pinene production was greatly improved by optimizing the expression of key enzymes. This is the first report on pinene produce by purple non-sulfur photosynthetic bacteria, which expands the availability of photosynthetic chassis for pinene production.


1988 ◽  
Vol 149 (5) ◽  
pp. 476-479 ◽  
Author(s):  
Michael Duchrow ◽  
Stefan Heitefuss ◽  
Jutta Kalkus ◽  
Michael Hoppert ◽  
Friedrich Giffhorn

1988 ◽  
Vol 66 (5) ◽  
pp. 442-448 ◽  
Author(s):  
Rafael Picorel ◽  
Gabriel Gingras

We have developed a simple and efficient method, using a mixed detergent system of sodium dodecyl sulfate and Triton X-100, for the preparative isolation of theB875 complex from Rhodobacter sphaeroides 2.4.1. As a bonus, the method allows the preparation of both the B875 and B800-850 complexes from the same batch of chromatophores. The preparations are spectrally pure, as indicated by absorption and circular dichroism spectroscopy. The latter method suggests that the Qy band of the B875 complex is due to weakly interacting bacteriochlorophyll molecules. Protein and pigment analysis shows that the B875 complex contains 2 mol of bacteriochlorophyll and 2 mol of sphaeroidene per mol of apoprotein (12 266 g), whereas the B800-850 complex contains 3 mol of bacteriochlorophyll and 1 mol of sphaeroidene per mol of apoprotein (11 497 g). While these stoichiometries are in accord with currently accepted models, they disagree with their published experimental basis. Phosphatidyl choline, phosphatidyl ethanolamine, phosphatidyl glycerol, and diphosphatidyl glycerol were found to be present in the B875 complex.


Gene ◽  
1988 ◽  
Vol 70 (1) ◽  
pp. 139-151 ◽  
Author(s):  
Tai Tsu-Ning ◽  
Mark D. Moore ◽  
Samuel Kaplan

BioHydrogen ◽  
2007 ◽  
pp. 123-131
Author(s):  
Lyudmila Vasilyeva ◽  
Masato Miyake ◽  
Masayuki Hara ◽  
Eiju Nakada ◽  
Satoshi Nishikata ◽  
...  

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