E. A. Doisy Department of Biochemistry, St. Louis University School of Medicine, St. Louis, Missouri 63104.
Plant Physiol. 1986 May;81(1):161-6. doi: 10.1104/pp.81.1.161.
Fractionation of Papaver bracteatum Arya II Lindl. latex on Renografin step gradients revealed that 43% of the dopamine was compartmentalized along with alpha-mannosidase (40%) in vacuoles sedimenting in the 2% fraction. Twenty-two percent of the dopamine was in the supernatant, but a corresponding amount (18%) of alpha-mannosidase was also present suggesting vacuole breakage during isolation. By subcellular fractionation of protoplasts from cultured P. bracteatum cells, the 1,000g sedimenting organelles have been identified as the major site of accumulation of the morphinan alkaloid, thebaine (99+/-0.8%), and the benzophenanthridine alkaloid, sanguinarine (96+/-3%). Although the 1,000g pellet also contained 33+/-4% of the total alkaloid precursor, dopamine, and half of the total vacuolar marker enzyme, alpha-mannosidase, 62+/-10% of the amine was localized in the 100,000g supernatant. A differential distribution of the alkaloids was discovered upon resolution of the lysed protoplasts on Renografin step gradients. Over 40% of the dopamine was in the supernatant with 15% in a 2% Renografin band. The remainder was evenly distributed in denser fractions of the gradient. The 4 to 8% interface, previously found to contain the largest amount of thebaine and small amounts of sanguinarine and dopamine, has been shown to be enriched in vacuoles by electron microscopy. Using a histofluorescence method, dopamine compartmentation in vacuoles of intact cultured cells was corroborated. In summary, dopamine, sanguinarine, and thebaine occur in vacuoles of different densities. A large fraction of the total dopamine in cultured cells was found in the 100,000g supernatant along with 37% of the alpha-mannosidase suggesting that the amine may be sequestered in more fragile vacuoles than the alkaloids. The possibility that some dopamine may be cytosolic cannot be ruled out.
从罂粟花乳状液经葡聚糖梯度离心,43%的多巴胺与α-甘露糖苷酶(40%)一起被分隔到 2%的组份中。22%的多巴胺存在于上清液中,但相应数量(18%)的α-甘露糖苷酶也存在,这表明在分离过程中出现了液泡破裂。通过培养的罂粟细胞原生质体的亚细胞分级分离,1000g 沉淀的细胞器被鉴定为吗啡生物碱蒂巴因(99+/-0.8%)和苯并菲啶生物碱血根碱(96+/-3%)的主要积累部位。虽然 1000g 沉淀也含有 33+/-4%的总生物碱前体多巴胺和一半的总液泡标记酶α-甘露糖苷酶,但 62+/-10%的胺定位于 100000g 的上清液中。在瑞诺格雷梯度上裂解原生质体后,发现生物碱的分布存在差异。超过 40%的多巴胺在上清液中,15%在 2%的瑞诺格雷带中。其余部分均匀分布在梯度的较密部分。先前发现含有大量蒂巴因和少量血根碱和多巴胺的 4-8%界面,通过电子显微镜显示富含液泡。使用组织荧光法,证实了完整培养细胞中多巴胺在液泡中的分隔。总之,多巴胺、血根碱和蒂巴因存在于不同密度的液泡中。在培养细胞中,发现大量的多巴胺(总多巴胺的 37%)与α-甘露糖苷酶一起存在于 100000g 的上清液中,这表明这种胺可能被隔离在比生物碱更脆弱的液泡中。不能排除一些多巴胺可能存在于细胞质中的可能性。