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THE PLANT CELL, Vol 5, Issue 12 1853-1863, Copyright © 1993 by American Society of Plant Biologists
Synechocystis sp PCC 6803 Strains Lacking Photosystem I and Phycobilisome Function
G. Shen, S. Boussiba and WFJ. Vermaas
Department of Botany and Center for the Study of Early Events in Photosynthesis, Arizona State University, Tempe, Arizona 85287-1601
To design an in vivo system allowing detailed analysis of photosystem II
(PSII) complexes without significant interference from other pigment
complexes, part of the psaAB operon coding for the core proteins of
photosystem I (PSI) and part of the apcE gene coding for the anchor protein
linking the phycobilisome to the thylakoid membrane were deleted from the
genome of the cyanobacterium Synechocystis sp strain PCC 6803. Upon
transformation and segregation at low light intensity (5 [mu]E m-2 sec-1),
a PSI deletion strain was obtained that is light tolerant and grows
reasonably well under photoheterotrophic conditions at 5 [mu]E m-2 sec-1
(doubling time ~28 hr). Subsequent inactivation of apcE by an erythromycin
resistance marker led to reduction of the phycobilin-to-chlorophyll ratio
and to a further decrease in light sensitivity. The resulting
PSI-less/apcE- strain grew photoheterotrophically at normal light intensity
(50 [mu]E m-2 sec-1) with a doubling time of 18 hr. Deletion of apcE in the
wild type resulted in slow photoautotrophic growth. The remaining
phycobilins in apcE- strains were inactive in transferring light energy to
PSII. Cells of both the PSI-less and PSI-less/apcE- strains had an
approximately sixfold enrichment of PSII on a chlorophyll basis and were as
active in oxygen evolution (on a per PSII basis) as the wild type at
saturating light intensity. Both PSI-less strains described here are highly
appropriate both for detailed PSII studies and as background strains to
analyze site- and region-directed PSII mutants in vivo.
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