CIL:39986, Phaeocystis antarctica, algae. In Cell Image Library ...

• Main Authors: Moisan, Tiffany, Sosinsky, Gina, Buitenhuys, Casey, Ellisman, Mark
• Format: Dataset
• Language: unknown
• Published: UC San Diego Library Digital Collections 2021
• Subjects: Phaeocystis antarctica; Chloroplast; thylakoid membrane organization; algae; photosynthetic electron transport chain; thylakoid; Antarc*; Antarctica
• Online Access: https://dx.doi.org/10.6075/j0gh9j4s; https://library.ucsd.edu/dc/object/bb9188821b

Preparation: glutaraldehyde fixed tissue; osmium tetroxide fixed tissue; tissue in epoxy resin embedment Relation to intact cell: microtome-sectioned tissue Imaging mode: illumination by electrons; detection of electrons Parameter imaged: electron density Source of contrast: stain with broad specificity Visualization methods: lead salt; uranyl salt; cationic colloidal gold Processing history: recorded image Data qualification: Processed ... : Culture conditions. Cultures of colonial P. antarctica (CCMP 1374) were grown semi-continuously for 5-8 generations in f/2 medium (Guillard and Ryther 1962) under continuous blue light at 4°C at irradiances of 14 and 259 µmol quanta m-2 s-1. Specific growth rate. Specific growth rate was estimated by a linear regression of loge transformed daily determinations of in vivo fluorescence intensity (n=2) measured with a Turner Model 10 fluorometer. Sample preparation for electron microscopy. P. antarctica colonies were fixed on ice with a 2% glutaraldehyde and 1.3% osmium tetroxide solution for 30 minutes and rinsed in distilled water. Cells were dehydrated through a series of ethanol: water washes (25:75, 50:50, 75:25, 95:5), three 100% ethanol washes and finally through three washes of 100% acetone. Cells were pelleted and fixed in an Epon resin. The fixation process lends itself to a breakup of the colonial matrix and we were able to examine P. antarctica individual colonial cells using electron tomography. ...