Putnam-Evans C, Bricker T M
Department of Biology, East Carolina University, Greenville, NC 27858, USA.
Plant Mol Biol. 1997 Jun;34(3):455-63. doi: 10.1023/a:1005826411702.
CP 47, a component of photosystem II (PSII) in higher plants, algae and cyanobacteria, is encoded by the psbB gene. Site-specific mutagenesis has been used to alter a portion of the psbB gene encoding the large extrinsic loop E of CP 47 in the cyanobacterium Synechocystis 6803. Alteration of a lysine residue occurring at position 321 to glycine produced a strain with altered PSII activity. This strain grew at wild-type rates in complete BG-11 media (480 microM chloride). However, oxygen evolution rates for this mutant in complete media were only 60% of the observed wild-type rates. Quantum yield measurements at low light intensities indicated that the mutant had 66% of the fully functional PSII centers contained in the control strain. The mutant proved to be extremely sensitive to photoinactivation at high light intensities, exhibiting a 3-fold increase in the rate of photoinactivation. When this mutant was grown in media depleted of chloride (30 microM chloride), it lost the ability to grow photoautotrophically while the control strain exhibited a normal rate of growth. The effect of chloride depletion on the growth rate of the mutant was reversed by the addition of 480 microM bromide to the chloride-depleted BG-11 media. In the presence of glucose, the mutant and control strains grew at comparable rates in either chloride-containing or chloride-depleted media. Oxygen evolution rates for the mutant were further depressed (28% of control rates) under chloride-limiting conditions. Addition of bromide restored these rates to those observed under chloride-sufficient conditions. Measurements of the variable fluorescence yield indicated that the mutant assembled fewer functional centers in the absence of chloride. These results indicate that the mutation K321G in CP 47 affects PSII stability and/or assembly under conditions where chloride is limiting.
CP 47是高等植物、藻类和蓝细菌中光系统II(PSII)的一个组分,由psbB基因编码。位点特异性诱变已被用于改变蓝细菌集胞藻6803中编码CP 47大的外在环E的psbB基因的一部分。将位于321位的赖氨酸残基改变为甘氨酸产生了一株PSII活性改变的菌株。该菌株在完全BG-11培养基(480微摩尔/升氯化物)中以野生型速率生长。然而,该突变体在完全培养基中的放氧速率仅为观察到的野生型速率的60%。低光强下的量子产率测量表明,该突变体具有对照菌株中所含全功能PSII中心的66%。该突变体被证明在高光强下对光失活极其敏感,光失活速率增加了3倍。当该突变体在缺乏氯化物(30微摩尔/升氯化物)的培养基中生长时,它失去了光自养生长的能力,而对照菌株表现出正常的生长速率。向缺乏氯化物的BG-11培养基中添加480微摩尔/升溴化物可逆转氯化物缺乏对突变体生长速率的影响。在有葡萄糖存在的情况下,突变体和对照菌株在含氯化物或缺乏氯化物的培养基中以相当的速率生长。在氯化物限制条件下,突变体的放氧速率进一步降低(为对照速率的28%)。添加溴化物可将这些速率恢复到氯化物充足条件下观察到的速率。可变荧光产率的测量表明,在没有氯化物的情况下,突变体组装的功能中心较少。这些结果表明,CP 47中的K321G突变在氯化物限制的条件下影响PSII的稳定性和/或组装。