Page 114 - Algae Anatomy, Biochemistry, and Biotechnology
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Anatomy                                                                      97
























                 FIGURE 2.66 A S. compressa zygote in bright field microscopy (a), and under fluorescence microscopy (b)
                 labeled with anti-rhodopsin antibody. The two arrows point to the cell membrane layer of the cell in which
                 photoreceptive protein are located. (Bar: 2 mm.)


                 protein was identified in the zygote membrane (Figure 2.66b). Because no eyespot can be detected
                 in these algal stages, the shading function is assigned to the whole cell body.
                     In the Haptophyta, the eyespot is present only in some species of the order Pavlovales. It con-
                 sists of a single layer of globules situated at the anterior end of one of the chloroplast, beneath the
                 posteriorly directed flagellum, at the level of its emersion from the cell. In these algae the photo-
                 receptor has not been yet localized, but we can presume it is positioned inside the membrane in
                 close association with the eyespot.
                     In the Cryptophyta, the presence of an eyespot is limited to a small number of species belonging
                 to the genus Chroomonas. The eyespot is situated in the center of the cell, within a conical lobe of
                 the chloroplast. It consists of a single layer of about 35 closely packed globules, attached to the
                 chloroplast envelope and the endoplasmic reticulum. Also in these algae the photoreceptive pro-
                 teins should be located inside the plasma membrane overlaying the eyespot.
                     In the Dinophyta, the eyespot is chloroplastic in Peridiniun sp., consisting of a layer of globules
                 under the chloroplast envelope, situated behind the longitudinal sulcus, and truly extraplastidic in
                 Woloszynskia coronata, where it consists of an irregular cluster of globules located beneath the
                 sulcus, and immediately adjacent to the subthecal microtubules. In the latter, neither connection
                 with the chloroplast nor membranes surrounding the eyespot are present. Glenodinium foliaceum
                 and Peridinium balticum possess another type of eyespot. It is a roughly triangular body situated
                 behind the sulcus and it is an independent structure bounded by a three-membrane envelope. Basi-
                 cally, there are two layers of pigmented globules, separated by a vesicle of granular material. The
                 eyespot can fold back upon itself, making more layers. In Amphidinium lacustre the eyespot is an
                 elongated structure located along the right edge of the sulcus. Its color is a shade of greenish-yellow
                 rather than the red-orange, commonly found in eyespot; it consists of up to six flat rows of brick-like
                 units, each row contained in a vesicle bounded by a unit membrane. No data exist on the photo-
                 receptor location in these dinoflagellates, but the assumption is the same made for the Haptophyta
                 and Cryptophyta, that is, photoreceptive proteins must be located inside the plasma membrane close
                 to the eyespot. A separate case is that of Alexandrium hiranoi and Gymnodinium mikimotoi. Both
                 dinoflagellates show phototactic responses but lack a detectable eyespot, hence the shading func-
                 tion is performed by the cell body.
                     In Chlorophyta such as Haematococcus sp., Spermatozopsis sp., and Dunaliella sp., the eyespot
                 is situated on one side of the cell, sometimes slightly protruding beyond the cell surface, as in the
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