Singh Abhay K, Sherman Louis A
Department of Biological Sciences, Purdue University, 1392 Lilly Hall of Life Sciences, West Lafayette, IN 47907, USA.
J Bacteriol. 2005 Apr;187(7):2368-76. doi: 10.1128/JB.187.7.2368-2376.2005.
The deletion of a gene coding for a histidine kinase (sll0750, Hik8) in the unicellular cyanobacterium Synechocystis sp. strain PCC 6803 resulted in a conditional lethal phenotype with a pleiotropic effect on the expression of genes involved in glucose metabolism. This mutant had comparable doubling times to wild type (WT) in continuous-light-grown photoautotrophic and mixotrophic cultures, whereas it grew poorly under mixotrophic conditions with different light and dark cycles. Growth was completely stopped, and cells eventually died, when the light duration was less than 6 h on a 24-h regimen. Northern blot analysis demonstrated that steady-state transcript levels of genes encoding key enzymes of glycolysis, gluconeogenesis, the oxidative pentose phosphate pathway, and glycogen metabolism were significantly altered in a strain with mutant hik8 (Deltahik8) grown with or without glucose. In some cases, differential expression was dependent on growth conditions (photoautotrophic versus mixotrophic). The enzyme activities of glucose-6-phosphate dehydrogenase, 6-phosphogluconate dehydrogenase, and phosphofructokinase were significantly reduced in Deltahik8 compared to WT. Glycogen determination indicated that Deltahik8 accumulated glycogen under mixotrophic conditions but was unable to utilize these reserves for heterotrophic growth. The results suggest that the loss of gap1 transcription in the absence of Hik8 was the key factor that rendered cells unable to catabolize glucose and grow heterotrophically. Additionally, the transcript levels of the phytochrome gene (cph1) and its cotranscribed response regulator gene (rcp1) were significantly reduced and its dark inducibility was lost in Deltahik8. The results demonstrated that Hik8 plays an important role in glucose metabolism and is necessary for heterotrophic growth.
在单细胞蓝藻集胞藻PCC 6803中,编码组氨酸激酶(sll0750,Hik8)的基因缺失导致了一种条件致死表型,对参与葡萄糖代谢的基因表达产生多效性影响。在连续光照培养的光合自养和混合营养培养中,该突变体与野生型(WT)的倍增时间相当,而在不同光照和黑暗周期的混合营养条件下生长较差。在24小时培养方案中,当光照时间少于6小时时,生长完全停止,细胞最终死亡。Northern印迹分析表明,在有或没有葡萄糖的情况下生长的突变体hik8(Deltahik8)菌株中,编码糖酵解、糖异生、氧化戊糖磷酸途径和糖原代谢关键酶的基因的稳态转录水平发生了显著变化。在某些情况下,差异表达取决于生长条件(光合自养与混合营养)。与WT相比,Deltahik8中葡萄糖-6-磷酸脱氢酶、6-磷酸葡萄糖酸脱氢酶和磷酸果糖激酶的酶活性显著降低。糖原测定表明,Deltahik8在混合营养条件下积累糖原,但无法利用这些储备进行异养生长。结果表明,在没有Hik8的情况下gap1转录的丧失是导致细胞无法分解代谢葡萄糖并进行异养生长的关键因素。此外,在Deltahik8中,光敏色素基因(cph1)及其共转录的响应调节基因(rcp1)的转录水平显著降低,并且其黑暗诱导性丧失。结果表明,Hik8在葡萄糖代谢中起重要作用,是异养生长所必需的。