Matsubayashi Y, Sakagami Y
Department of Applied Biological Sciences, Nagoya University, Chikusa, Japan.
Proc Natl Acad Sci U S A. 1996 Jul 23;93(15):7623-7. doi: 10.1073/pnas.93.15.7623.
Proliferation of dispersed plant cells in culture is strictly dependent on cell density, and cells in a low-density culture can only grow in the presence of conditioned medium (CM). No known plant hormones have been able to substitute for CM. To quantify the mitogenic activity of CM, we examined conditions for the assay system using mechanically dispersed mesophyll cells of Asparagus officinalis L. and established a highly sensitive bioassay method. By use of this method, the mitogenic activity of CM prepared from asparagus cells was characterized: it was heat-stable, susceptible to pronase digestion, and resistant to glycosidase treatment. On the basis of these results, the mitogenic activity in CM was purified 10(7)-fold by column chromatography, and two factors named phytosulfokine-alpha and -beta (PSK-alpha and PSK-beta) were obtained. By amino acid sequence analysis and mass spectrometry, the structures of these two factors were determined to be sulfated pentapeptide (H-Tyr(SO3H)-Ile-Tyr(SO3H)-Thr-Gln-OH) and sulfated tetrapeptide (H-Tyr(SO3H)-Ile-Tyr(SO3H)-Thr-OH). PSK-alpha and PSK-beta were prepared by chemical synthesis and enzymatic sulfation. The synthetic peptides exhibited the same activity as the natural factors, confirming the structure for PSK-alpha and PSK-beta mentioned above. This is the first elucidation of the structure of a conditioned medium factor required for the growth of low-density plant cell cultures.
培养中分散的植物细胞增殖严格依赖于细胞密度,低密度培养中的细胞只有在条件培养基(CM)存在时才能生长。尚无已知植物激素能够替代CM。为了量化CM的促有丝分裂活性,我们使用芦笋机械分散的叶肉细胞研究了检测系统的条件,并建立了一种高灵敏度的生物检测方法。通过使用该方法,对芦笋细胞制备的CM的促有丝分裂活性进行了表征:它对热稳定,易受链霉蛋白酶消化,且对糖苷酶处理有抗性。基于这些结果,通过柱色谱法将CM中的促有丝分裂活性纯化了10^7倍,获得了两种因子,分别命名为植物磺肽素-α和-β(PSK-α和PSK-β)。通过氨基酸序列分析和质谱分析,确定这两种因子的结构分别为硫酸化五肽(H-Tyr(SO3H)-Ile-Tyr(SO3H)-Thr-Gln-OH)和硫酸化四肽(H-Tyr(SO3H)-Ile-Tyr(SO3H)-Thr-OH)。PSK-α和PSK-β通过化学合成和酶促硫酸化制备。合成肽表现出与天然因子相同的活性,证实了上述PSK-α和PSK-β的结构。这是首次阐明低密度植物细胞培养生长所需的条件培养基因子的结构。