Konomi K, Furuya M, Yamamoto K T, Yokota T, Takahashi N
Department of Biology, Faculty of Science, University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113, Japan.
Plant Physiol. 1982 Jul;70(1):307-10. doi: 10.1104/pp.70.1.307.
Soyasaponin I, a triterpenoid saponin isolated from etiolated pea (Pisum sativum cv. Alaska) shoots and identified as Pfr killer, was examined for its effects on spectral properties of undegraded pea phytochrome. When soyasaponin I in concentrations of 100 micromolar or lower was added to Pr in the dark, the spectrum of Pr was not significantly affected, whereas in the presence of 120 micromolar or higher concentrations the absorption maximum of Pr shifted from 666 to 658 nanometer with slight decrease of absorbance. After a brief exposure of the mixture to red light, the increase in absorbance at 666 nanometers that occurs in the dark was inhibited at 26 micromolar and higher soyasaponin I concentrations; the maximum effect being reached at about 180 micromolar. The decrease in absorbance at 724 nanometers in the dark after red light irradiation was somewhat inhibited by 60 micromolar and totally prevented by 410 micromolar soyasaponin I. When P(658) was irradiated with red light in the presence of 220 micromolar or higher soyasaponin I concentrations, a bleached form (P(bl)) was produced instead of Pfr. P(bl) showed no dark spectral changes, and the phototransformation of P(bl) to P(658) required a significantly high irradiance of far-red light. When the saponin was added to Pfr in the dark, none of the above-described spectral changes occurred, although the same effects were observed after the mixture was exposed briefly to far-red light followed by red light.
大豆皂苷I是一种从黄化豌豆(豌豆品种阿拉斯加)芽中分离出来的三萜皂苷,被鉴定为Pfr杀手,研究了其对未降解豌豆光敏色素光谱特性的影响。当在黑暗中将浓度为100微摩尔或更低的大豆皂苷I添加到Pr中时,Pr的光谱没有受到显著影响,而在120微摩尔或更高浓度存在下,Pr的吸收最大值从666纳米移至658纳米,吸光度略有下降。将混合物短暂暴露于红光后,在黑暗中666纳米处吸光度的增加在大豆皂苷I浓度为26微摩尔及更高时受到抑制;在约180微摩尔时达到最大效果。红光照射后黑暗中724纳米处吸光度的下降在60微摩尔时受到一定抑制,在410微摩尔大豆皂苷I时完全被阻止。当在220微摩尔或更高浓度的大豆皂苷I存在下用红光照射P(658)时,产生的是漂白形式(P(bl))而不是Pfr。P(bl)在黑暗中没有光谱变化,并且P(bl)向P(658)的光转化需要显著高的远红光辐照度。当在黑暗中将皂苷添加到Pfr中时,上述光谱变化均未发生,尽管在混合物短暂暴露于远红光后再暴露于红光后观察到了相同的效果。