Regulation of the steady-state levels of B800-850 complexes in Rhodobacter capsulatus by light and oxygen

• Main Author: Zucconi, Anthony
• Language: English
• Published: University of British Columbia 2010
• Subjects: Rhodobacter capsulatus; Peptides > Physiological effect; Peptides > physiology; Light > Physiological effect; Photosynthesis > Regulation
• Online Access: http://hdl.handle.net/2429/28362

Photosynthetic organisms exhibit a variety of responses to changes in light intensity, including differential biosynthesis of chlorophyll-protein complexes. Cultures of Rhodobacter capsulatus grown anaerobically with a low intensity of light (2 W/m²) contained about four times as much B800-850 light harvesting complex as cells grown under high light intensity (140 W/m²). The mRNA transcripts encoding B800-850 beta and alpha peptides were analyzed by Northern blot, S1 nuclease protection and capping with guanylyl transferase. It was found that the steady-state levels of B800-850 mRNAs in high light-grown cultures was about four times as great as in cells grown under low light intensity. Therefore the lesser amounts of mature B800-850 peptide gene products found in cells grown with high light intensity were the result of a posttranscriptional regulatory process. It was also found that there were two polycistronic messages encoding the B800-850 peptides. These messages shared a common 3' terminus but differed in their 5' end segments as a result of transcription initiation at two discrete sites. Moreover the half life of B800-850 mRNAs was about 10 minutes in cells grown with high light and approximately 19 minutes in low light-grown cultures. Transcriptional and translational fusions were constructed between the B800-850 transcription initiation region (from this point on referred to as the puc transcription initiation region; see Fig. 1) and the Escherichia coli lacZ gene. From these studies it was concluded that the rates of transcription initiation of the puc (B800-850) genes was higher in cells grown with high light illumination than in low light-grown cultures, and that the relative amount of B800-850 complexes under these conditions was controlled by a translational or a posttranslational mechanism. The translational and transcriptional fusions were also used for examination of oxygen regulated expression of the puc genes. === Science, Faculty of === Microbiology and Immunology, Department of === Graduate