Both animal fats and plant oils are made up of glycerol and fatty acids. It is actually a carboxylic acid that contains a hydrocarbon chain and also a terminal carboxyl group. It can be either in saturated or unsaturated form. I hope that this answer has come to your help.
New borns getting breast milk would need parental nutrition
The statement 'a cell poisoned by a substance that inactivates the Golgi body would have immediate difficulty in the synthesis of lipids' is TRUE. It is a fundamental organelle.
<h3>What is the Golgi apparatus?</h3>
The Golgi apparatus is an organelle present in eukaryotic cells that function for transporting, altering the composition, and packaging of different biomolecules.
The Golgi apparatus processes and sorts biomolecules such as proteins, and different types of lipids.
The different types of lipids that are modified in the Golgi apparatus include glycolipids and sphingomyelin.
Learn more about the Golgi apparatus here:
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Answer:
true
Explanation:
Most detected neutron stars are pulsars, and emit radio-frequency electromagnetic radiation.
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There are three types of galactosemia depending on enzyme deficiency.
<span>1. <span>Classic galactosemia which is an inborn autosomal recessive metabolic disorder which is caused by a deficiency of the enzyme galactose-1-phosphate uridylyltransferase. Classic galactosemia will result in accumulation of galactose-1-phosphate, galactose, and its derivatives, galactitol and galactonate.</span></span>
<span>2. Galactokinase deficiency is also an autosomal recessive metabolic disorder which results in accumulation of galactose and galactitol because </span><span>conversion of galactose to </span>galactose-1-phosphate <span> by </span><span>galactokinase is decreased</span>.
<span>3. <span>Galactose epimerase deficiency is an autosomal recessive disorder which is a result of a deficiency of the enzyme galactose epimerase. This disorder leads to the accumulation of galactose and galactose-1-phosphate.</span></span>
