Klut M E, Bisalputra T, Antia N J
Department of Botany, University of British Columbia, Vancouver, Canada.
Histochem J. 1988 Jan;20(1):35-40. doi: 10.1007/BF01745967.
Sixteen fluorochromes were tested for the cytochemical characterization of two dinoflagellates (Amphidinuim carterae, Prorocentrum micans) and one chlorophycean flagellate (Dunaliella tertiolecta). Depending on the fluorochrome used, various cellular components (including the plasma membrane, thecal plates, pusule, trichocysts, nucleus, lipid bodies and vacuoles) were revealed. The different colours obtained from single or double fluorochrome staining enabled the differentiation and identification of most cellular components. Protoplasmic staining with Fluorescein diacetate suggested the occurrence of esterases in the three phytoflagellates. Rhodamine B, Neutral Red, FluoroBora P and Nile Blue revealed extensive occurrence of lipoid bodies in A. carterae, but Nile Blue showed considerable difference from the other stains in the inclusion size and intracellular location of these bodies. Chlortetracycline binding, and its inhibition by the Ca2+ionophore A23187, indicated that the plasma membrane, pusule system and trichocysts contain sites of Ca2+ binding. Calcofluor White ST proved superior to Congo Red and Lucifer Yellow in elucidating structural details of the thecal plates of P. micans. While Acridine Orange revealed the presence of surface-coat acidic polysaccharides, the fluoresceinated lectins established their glycoconjugate nature in all the three flagellates. Possible mechanisms of fluorochrome uptake are discussed.
对16种荧光染料进行了测试,以对两种甲藻(卡特双鞭甲藻、海洋原甲藻)和一种绿藻鞭毛虫(杜氏盐藻)进行细胞化学特征分析。根据所使用的荧光染料,可显示出各种细胞成分(包括质膜、板片、液泡、刺丝囊、细胞核、脂质体和液泡)。通过单荧光染料或双荧光染料染色获得的不同颜色能够区分和识别大多数细胞成分。用荧光素二乙酸酯进行原生质染色表明这三种植物性鞭毛虫中存在酯酶。罗丹明B、中性红、氟硼P和尼罗蓝显示卡特双鞭甲藻中大量存在脂质体,但尼罗蓝在这些脂质体的包涵体大小和细胞内位置方面与其他染料有显著差异。金霉素结合及其被Ca2+离子载体A23187抑制表明质膜、液泡系统和刺丝囊含有Ca2+结合位点。在阐明海洋原甲藻板片的结构细节方面,荧光增白剂ST比刚果红和荧光素黄更具优势。虽然吖啶橙显示存在表面包被酸性多糖,但荧光素化凝集素确定了所有这三种鞭毛虫中它们的糖缀合物性质。讨论了荧光染料摄取的可能机制。