Control of light-dependent keto carotenoid biosynthesis in Nostoc 7120 by the transcription factor NtcA.

In Nostoc PCC 7120, two different ketolases, CrtW and CrtO are involved in the formation of keto carotenoids from ß-carotene. In contrast to other cyanobacteria, CrtW catalyzes the formation of monoketo echinenone whereas CrtO is the only enzyme for the synthesis of diketo canthaxanthin. This is the major photo protective carotenoid in this cyanobacterium. Under high-light conditions, basic canthaxanthin formation was transcriptionally up-regulated. Upon transfer to high light, the transcript levels of all investigated carotenogenic genes including those coding for phytoene synthase, phytoene desaturase and both ketolases were increased. These transcription changes proceeded via binding of the transcription factor NtcA to the promoter regions of the carotenogenic genes. The binding was absolutely dependent on the presence of reductants and oxo-glutarate. Light-stimulated transcript formation was inhibited by DCMU. Therefore, photosynthetic electron transport is proposed as the sensor for high-light and a changing redox state as a signal for NtcA binding.

Multiple ketolases involved in light regulation of canthaxanthin biosynthesis in Nostoc punctiforme PCC 73102.

In the genome of Nostoc punctiforme PCC 73102, three functional ß-carotene ketolase genes exist, one of the crtO and two of the crtW type. They were all expressed and their corresponding enzymes were functional inserting 4-keto groups into ß-carotene as shown by functional pathway complementation in Escherichia coli. They all synthesized canthaxanthin but with different efficiencies. Canthaxanthin is the photoprotective carotenoid of N. punctiforme PCC 73102. Under high-light stress, its synthesis was enhanced. This was caused by up-regulation of the transcripts of two genes in combination. The first crtB-encoding phytoene synthase is the gate way enzyme of carotenogenesis resulting in an increased inflow into the pathway. The second was the ketolase gene crtW148 which in high light takes over ß-carotene conversion into canthaxanthin from the other ketolases. The other ketolases were down-regulated under high-light conditions. CrtW148 was also exclusively responsible for the last step in 4-keto-myxoxanthophyll synthesis.

First dinuclear B(II) monocations with bridging guanidinate ligands: synthesis and properties.

Reaction between the diborane (4) B2Cl2(NMe2)2 and Li(hpp) (hpp-=1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidinate) leads to [(Me2N)B(mu-hpp)] 2. This species can be protonated by HCl.OEt2 to give [(Me2HN)B(mu-hpp)]2Cl2 featuring two B(II) cations with direct B-B bonding. The unsymmetrical monocation [(Me2N)B2(mu-hpp)2(NHMe2)]+ is also obtained. [(Me2HN)B(mu-hpp)]2Cl2 eliminates NHMe2 in a slow reaction leading to [ClB2(mu-hpp)2(NHMe2)]Cl and ultimately, presumably, to [ClB(mu-hpp)]2. We report the crystal structures of the two monocations [ClB2(mu-hpp)2(NHMe2)]Cl and [(Me2N)B2(mu-hpp)2(NHMe2)]Cl. The experimental results are accompanied by some quantum chemical density-functional theory calculations.