Green P B, Erickson R O, Buggy J
Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania 19104.
Plant Physiol. 1971 Mar;47(3):423-30. doi: 10.1104/pp.47.3.423.
Several levels of control of elongation rate are revealed through the detailed study of responses of the Nitella internode to abrupt shifts in turgor. The immediate response, which apparently reflects the physical state of the cell, is approximately described by the equation r = (P - Y)m where r is rate, P is pressure, Y is the wall's yielding threshold, and m is related to the wall's apparent fluidity (reciprocal viscosity). Because P and Y are in the range 5 to 6 atmospheres, and (P - Y) is roughly 0.2 atmosphere, elongation rate is initially extremely sensitive to changes in P. A small step-down in turgor (0.7 atmosphere) stops growth, and a similar rise greatly accelerates it. These initial responses are, however, soon (15 minutes) compensated by changes in Y. An apparent metabolism-dependent reaction (azide-sensitive) lowers Y; strain hardening (azide-insensitive) raises it. These two opposing processes, acting on Y, serve as a governor on (P - Y), tending to maintain it at a given value despite changes in P. This ability to compensate is itself a function of turgor. Turgor step-downs are less and less well compensated, leading to lower rate, as turgor falls from 5 atmospheres to about 2 atmospheres where growth appears not to resume. This is the lowest attainable yield value, Y(1). The turgor dependency of compensation reflects a turgor requirement of the Y-lowering ("wall-softening") process. Thus the relation between steady state, r(s), and turgor is an indirect one, derived from time-dependent alterations of the cell wall. This relationship superficially resembles the instantaneously valid one in that, roughly, r(s) = (P - Y(1))m(s). Y(1) and m(s), however, have much lower values than Y and m. The duality of the elongation rate versus turgor relation and the prominent role of Y in regulating rate are the major features of growth control in Nitella.
通过对丽藻节间对膨压突然变化的反应进行详细研究,揭示了伸长率的几个控制水平。直接反应显然反映了细胞的物理状态,大约由方程r = (P - Y)m描述,其中r是速率,P是压力,Y是细胞壁的屈服阈值,m与细胞壁的表观流动性(倒数粘度)有关。由于P和Y在5至6个大气压的范围内,且(P - Y)约为0.2个大气压,伸长率最初对P的变化极为敏感。膨压小幅下降(0.7个大气压)会停止生长,类似的上升则会极大地加速生长。然而,这些初始反应很快(15分钟)就会被Y的变化所补偿。一种明显的依赖代谢的反应(对叠氮化物敏感)会降低Y;应变硬化(对叠氮化物不敏感)会提高Y。这两个作用于Y的相反过程,起到了对(P - Y)的调节作用,尽管P发生变化,仍倾向于将其维持在给定值。这种补偿能力本身是膨压的函数。随着膨压从5个大气压降至约2个大气压,膨压下降得到的补偿越来越少,导致生长速率降低,此时生长似乎无法恢复。这是可达到的最低屈服值Y(1)。补偿的膨压依赖性反映了降低Y(“细胞壁软化”)过程对膨压的需求。因此,稳态伸长率r(s)与膨压之间的关系是间接的,源自细胞壁随时间的变化。这种关系表面上类似于即时有效的关系,大致为r(s) = (P - Y(1))m(s)。然而,Y(1)和m(s)的值比Y和m低得多。伸长率与膨压关系的二元性以及Y在调节速率中的突出作用是丽藻生长控制的主要特征。