Erickson Harold P
Department of Cell Biology, Duke University Medical Center, Durham, NC, United States.
Front Microbiol. 2021 May 10;12:664704. doi: 10.3389/fmicb.2021.664704. eCollection 2021.
The cytoplasm of bacteria is maintained at a higher osmolality than the growth medium, which generates a turgor pressure. The cell membrane (CM) cannot support a large turgor, so there are two possibilities for transferring the pressure to the peptidoglycan cell wall (PGW): (1) the CM could be pressed directly against the PGW, or (2) the CM could be separated from the PGW by a periplasmic space that is isoosmotic with the cytoplasm. There is strong evidence for gram-negative bacteria that a periplasm exists and is isoosmotic with the cytoplasm. No comparable studies have been done for gram-positive bacteria. Here I suggest that a periplasmic space is probably essential in order for the periplasmic proteins to function, including especially the PBPs that remodel the peptidoglycan wall. I then present a semi-quantitative analysis of how teichoic acids could support a periplasm that is isoosmotic with the cytoplasm. The fixed anionic charge density of teichoic acids in the periplasm is ∼0.5 M, which would bring in ∼0.5 M Na neutralizing ions. This approximately balances the excess osmolality of the cytoplasm that would produce a turgor pressure of 19 atm. The 0.5 M fixed charge density is similar to that of proteoglycans in articular cartilage, suggesting a comparability ability to support pressure. An isoosmotic periplasm would be especially important for cell division, since it would allow CM constriction and PGW synthesis to avoid turgor pressure.
细菌的细胞质渗透压维持在高于生长培养基的水平,从而产生膨压。细胞膜(CM)无法承受较大的膨压,因此将压力传递至肽聚糖细胞壁(PGW)有两种可能方式:(1)细胞膜可直接挤压肽聚糖细胞壁;(2)细胞膜可通过与细胞质等渗的周质空间与肽聚糖细胞壁分离。有确凿证据表明革兰氏阴性菌存在周质空间且与细胞质等渗。对于革兰氏阳性菌尚未开展类似研究。在此我认为周质空间对于周质蛋白发挥功能可能至关重要,尤其是对于重塑肽聚糖壁的青霉素结合蛋白(PBPs)。接着我对磷壁酸如何支持与细胞质等渗的周质进行了半定量分析。周质中磷壁酸的固定阴离子电荷密度约为0.5 M,这会引入约0.5 M的Na⁺中和离子。这大致平衡了细胞质中会产生19个大气压膨压的过量渗透压。0.5 M的固定电荷密度与关节软骨中的蛋白聚糖相似,表明其具有类似的承受压力能力。等渗周质对于细胞分裂尤为重要,因为它能使细胞膜收缩和肽聚糖细胞壁合成避免膨压。