Cells Flashcards
(68 cards)
Describe The Nuclear Envelope
Continuous Double membrane that surrounds the cell
Describe The Nucleoplasm
Makes up the bulk of nucleus and contains chromatin
What is the function of nuclear pores
Allow passage of ribosomes and messenger RNA
Describe the nucleolus
Dark centre within nucleoplasm it manufactures ribosomes
What are the Differences of smooth and rough endoplasmic reticulum
•Rough has ribosomes on and is involved in synthesis of protein
•Smooth synthesises carbohydrates and lipids
What are the similarities of smooth and rough endoplasmic reticulum
•Both consist of flattened sacks and tubules to increase surface area
•both are connected to the outer membrane of the nucleus
What are the structures of a mitochondria
•double membrane
•Cristae (folded inner membrane)
•Matrixm
Describe the mitrochondria cristae
Folded inner membrane needed to increase surface area for attachment of enzymes for respiration
Describe the mitochondria matrix
Makes up remainder of mitochondria and contains DNA ribosomes and enzymes for respiration
What are the structures of a chloroplast
•Chloroplast envelope (double membrane)
•thylakoids and grana
•lamella
•Stroma
Describe the thylakoid
Folded membranes containing chlorophyll pigment
Describe the grana
Stack of multiple thylakoids attached by lamella
Describe the stroma
Fluid filled matrix containing ribosomes to make enzymes for photosynthesis
Describe the Golgi apparatus’s job
Modifies, sorts, and packages proteins and lipids for secretion or delivery to other parts of the cell
What happen to proteins, carbohydrates and lipids in the Golgi body
Carbohydrates can be added and lipids and proteins are labelled them and forms vesicles and leave the cell
What are differences of transmission electron microscopes and scanning electron microscope
•scanning has a 3d image where cells are coated in a metal, no dissection needed
•Transmission has 2d image where cells are stained with Metal it has a higher resolution but cells need to be dissected
What are the steps of cell fractionation
Homogenisation.—>filtration—> Differential centrifugal
Negatives of transmission electron microscopes
Difficult to prepare the slide as needs to be cut thin for electrons to pass through, cells will be dead as it’s in a vacuum in black and white it’s also expensive
What are the steps to cell fractionation
Homogenisation—>filtration—>differential centrifugation
Describe the buffer solution used before cell fractionation
Is cold to prevent enzyme denaturing and slow down metabolic processes
•it has the same water potential as the cell to prevent it bursting
What happens during differential centrifugation
Cellular components are separated off by spinning samples at various speeds larger particles settle to bottom of tube first followed by lighter as speed increases
What is the order of the mitosis
Prophase—>Metaphase—> Anaphase —>Telophase
What happens during prophase
•Chromatin condense and form chromosome
•centrioles begin to form spindle fibres
• nuclear envelope breaks down
What happens during metaphase
Chromosome align along equatorial plate
Spindle fibres attach