A1 Refereed original research article in a scientific journal
OVER-PRODUCTION OF THE D1 PROTEIN OF PHOTOSYSTEM-II REACTION-CENTER IN THE CYANOBACTERIUM SYNECHOCOCCUS SP PCC-7942
Authors: SOITAMO AJ, ZHOU G, CLARKE AK, OQUIST G, ARO EM, GUSTAFSSON P
Publisher: KLUWER ACADEMIC PUBL
Publication year: 1994
Journal:: Plant Molecular Biology
Journal name in source: PLANT MOLECULAR BIOLOGY
Journal acronym: PLANT MOL BIOL
Volume: 26
Issue: 2
First page : 709
Last page: 721
Number of pages: 13
ISSN: 0167-4412
DOI: https://doi.org/10.1007/BF00013756
Abstract
The unicellular cyanobacterium Synechococcus sp. PCC 7942 has three psbA genes encoding two different forms of the photosystem II reaction centre protein D1 (D1:1 and D1:2). The level of expression of these psbA genes and the synthesis of D1:1 and D1:2 are strongly regulated under varying light conditions. In order to better understand the regulatory mechanisms underlying these processes, we have constructed a strain of Synechococcus sp. PCC 7942 capable of over-producing psbA mRNA and D1 protein. In this study, we describe the over-expression of D1:1 using a tac-hybrid promoter in front of the psbAI gene in combination with lacI(Q) repressor system. Over-production of D1:1 was induced by growing cells for 12 h at 50 mu mol photons m(-2) s(-1) in the presence of 40 or 80 mu g/ml IPTG. The amount of psbAI mRNA and that of D1:1 protein in cells grown with IPTG was three times and two times higher, respectively. A higher concentration of IPTG (i.e., 150 mu g/ml) did not further increase the production of the psbAI message or D1:1. The over-production of D1:1 caused a decrease in the level of D1:2 synthesised, resulting in most PSII reaction centres containing D1:1. However, the over-production of D1:1 had no effect on the pigment composition (chlorophyll a or phycocyanin/number of cells) or the light-saturated rate of photosynthesis. This and the fact that the total amounts of D1 and D2 proteins were not affected by IPTG suggest that the number of PSII centres within the membranes remained unchanged. From these results, we conclude that expression of psbAI can be regulated by using the tac promoter and lacI(Q) system. However, the accumulation of D1:1 protein into the membrane is regulated by the number of PSII centres.
The unicellular cyanobacterium Synechococcus sp. PCC 7942 has three psbA genes encoding two different forms of the photosystem II reaction centre protein D1 (D1:1 and D1:2). The level of expression of these psbA genes and the synthesis of D1:1 and D1:2 are strongly regulated under varying light conditions. In order to better understand the regulatory mechanisms underlying these processes, we have constructed a strain of Synechococcus sp. PCC 7942 capable of over-producing psbA mRNA and D1 protein. In this study, we describe the over-expression of D1:1 using a tac-hybrid promoter in front of the psbAI gene in combination with lacI(Q) repressor system. Over-production of D1:1 was induced by growing cells for 12 h at 50 mu mol photons m(-2) s(-1) in the presence of 40 or 80 mu g/ml IPTG. The amount of psbAI mRNA and that of D1:1 protein in cells grown with IPTG was three times and two times higher, respectively. A higher concentration of IPTG (i.e., 150 mu g/ml) did not further increase the production of the psbAI message or D1:1. The over-production of D1:1 caused a decrease in the level of D1:2 synthesised, resulting in most PSII reaction centres containing D1:1. However, the over-production of D1:1 had no effect on the pigment composition (chlorophyll a or phycocyanin/number of cells) or the light-saturated rate of photosynthesis. This and the fact that the total amounts of D1 and D2 proteins were not affected by IPTG suggest that the number of PSII centres within the membranes remained unchanged. From these results, we conclude that expression of psbAI can be regulated by using the tac promoter and lacI(Q) system. However, the accumulation of D1:1 protein into the membrane is regulated by the number of PSII centres.
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