- Describe how lipids are catabolized
- Describe how lipid catabolism can be used to identify microbes
- Describe how proteins are catabolized
- Describe how protein catabolism can be used to identify bacteria
Previous sections have discussed the catabolism of glucose, which provides energy to living cells, as well as how polysaccharides like glycogen, starch, and cellulose are degraded to glucose monomers. But microbes consume more than just carbohydrates for food. In fact, the microbial world is known for its ability to degrade a wide range of molecules, both naturally occurring and those made by human processes, for use as carbon sources. In this section, we will see that the pathways for both lipid and protein catabolism connect to those used for carbohydrate catabolism, eventually leading into glycolysis, the transition reaction, and the Krebs cycle pathways. Metabolic pathways should be considered to be porous—that is, substances enter from other pathways, and intermediates leave for other pathways. These pathways are not closed systems. Many of the substrates, intermediates, and products in a particular pathway are reactants in other pathways.
Triglycerides are a form of long-term energy storage in animals. They are made of glycerol
and three fatty acids
(see Figure 1 in Lipids
). Phospholipids compose the cell and organelle membranes of all organisms except the archaea. Phospholipid structure is similar to triglycerides
except that one of the fatty acids is replaced by a phosphorylated head group (see Figure 2 in Lipids
). Triglycerides and phospholipids
are broken down first by releasing fatty acid chains (and/or the phosphorylated head group, in the case of phospholipids) from the three-carbon glycerol backbone. The reactions breaking down triglycerides are catalyzed by lipases
and those involving phospholipids are catalyzed by phospholipases
. These enzymes contribute to the virulence of certain microbes, such as the bacterium Staphylococcus aureus
and the fungus Cryptococcus neoformans
. These microbes use phospholipases to destroy lipids and phospholipids in host cells and then use the catabolic products for energy (see Virulence Factors of Bacterial and Viral Pathogens
The resulting products of lipid catabolism, glycerol and fatty acids, can be further degraded. Glycerol can be phosphorylated to glycerol-3-phosphate and easily converted to glyceraldehyde 3-phosphate, which continues through glycolysis. The released fatty acids are catabolized in a process called β-oxidation
, which sequentially removes two-carbon acetyl groups from the ends of fatty acid chains, reducing NAD+
and FAD to produce NADH and FADH2
, respectively, whose electrons can be used to make ATP by oxidative phosphorylation. The acetyl groups produced during β-oxidation are carried by coenzyme A to the Krebs cycle, and their movement through this cycle results in their degradation to CO2
, producing ATP by substrate-level phosphorylation and additional NADH and FADH2
molecules (see Metabolic Pathways
for a detailed illustration of β-oxidation).
Other types of lipids can also be degraded by certain microbes. For example, the ability of certain pathogens, like Mycobacterium tuberculosis
, to degrade cholesterol contributes to their virulence. The side chains of cholesterol can be easily removed enzymatically, but degradation of the remaining fused rings is more problematic. The four fused rings are sequentially broken in a multistep process facilitated by specific enzymes, and the resulting products, including pyruvate, can be further catabolized in the Krebs cycle.
Think about It
- How can lipases and phospholipases contribute to virulence in microbes?
Proteins are degraded through the concerted action of a variety of microbial protease
enzymes. Extracellular proteases cut proteins internally at specific amino acid sequences, breaking them down into smaller peptides that can then be taken up by cells. Some clinically important pathogens can be identified by their ability to produce a specific type of extracellular protease. For example, the production of the extracellular protease gelatinase
by members of the genera Proteus
can be used to distinguish them from other gram-negative enteric bacteria. Following inoculation and growth of microbes in gelatin broth, degradation of the gelatin protein due to gelatinase production prevents solidification of gelatin when refrigerated. Other pathogens can be distinguished by their ability to degrade casein, the main protein found in milk. When grown on skim milk agar, production of the extracellular protease caseinase
causes degradation of casein, which appears as a zone of clearing around the microbial growth. Caseinase production by the opportunist pathogen Pseudomonas aeruginosa
can be used to distinguish it from other related gram-negative bacteria.
After extracellular protease degradation and uptake of peptides in the cell, the peptides can then be broken down further into individual amino acids by additional intracellular proteases, and each amino acid can be enzymatically deaminated to remove the amino group. The remaining molecules can then enter the transition reaction or the Krebs cycle.
Think about It
- How can protein catabolism help identify microbes?
Clinical Focus: Alex, Part 3
This example continues Alex’s story that started in Energy Matter and Enzymes
Because bacterial meningitis progresses so rapidly, Alex’s doctors had decided to treat him aggressively with antibiotics, based on empirical observation of his symptoms. However, laboratory testing to confirm the cause of Alex’s meningitis was still important for several reasons. N. meningitidis
is an infectious pathogen that can be spread from person to person through close contact; therefore, if tests confirm N. meningitidis
as the cause of Alex’s symptoms, Alex’s parents and others who came into close contact with him might need to be vaccinated or receive prophylactic antibiotics to lower their risk of contracting the disease. On the other hand, if it turns out that N. meningitidis
is not the cause, Alex’s doctors might need to change his treatment.
The clinical laboratory performed a Gram stain on Alex’s blood and CSF samples. The Gram stain showed the presence of a bean-shaped gram-negative diplococcus. The technician in the hospital lab cultured Alex’s blood sample on both blood agar and chocolate agar, and the bacterium that grew on both media formed gray, nonhemolytic colonies. Next, the technician performed an oxidase test on this bacterium and determined that it was oxidase positive. Last, he examined the repertoire of sugars that the bacterium could use as a carbon source and found that the bacterium was positive for glucose and maltose use but negative for lactose and sucrose use. All of these test results are consistent with characteristics of N. meningitidis
- What do these test results tell us about the metabolic pathways of N. meningitidis?
- Why do you think that the hospital used these biochemical tests for identification in lieu of molecular analysis by DNA testing?
We’ll return to Alex’s example in later pages.
Key Concepts and Summary
- Collectively, microbes have the ability to degrade a wide variety of carbon sources besides carbohydrates, including lipids and proteins. The catabolic pathways for all of these molecules eventually connect into glycolysis and the Krebs cycle.
- Several types of lipids can be microbially degraded. Triglycerides are degraded by extracellular lipases, releasing fatty acids from the glycerol backbone. Phospholipids are degraded by phospholipases, releasing fatty acids and the phosphorylated head group from the glycerol backbone. Lipases and phospholipases act as virulence factors for certain pathogenic microbes.
- Fatty acids can be further degraded inside the cell through β-oxidation, which sequentially removes two-carbon acetyl groups from the ends of fatty acid chains.
- Protein degradation involves extracellular proteases that degrade large proteins into smaller peptides. Detection of the extracellular proteases gelatinase and caseinase can be used to differentiate clinically relevant bacteria.
Which of the following molecules is not produced during the breakdown of phospholipids?
- acetyl groups
- fatty acids
Answer a. Glucose is not produced during the breakdown of phospholipids?
Caseinase is which type of enzyme?
- extracellular protease
- intracellular protease
Answer c. Caseinase is a extracellular protease.
Which of the following is the first step in triglyceride degradation?
- removal of fatty acids
- breakage of fused rings
- formation of smaller peptides
Answer a. The removal of fatty acids is the first step in triglyceride degradation.
Fill in the Blank
The process by which two-carbon units are sequentially removed from fatty acids, producing acetyl-CoA, FADH2
, and NADH is called ________.
The process by which two-carbon units are sequentially removed from fatty acids, producing acetyl-CoA, FADH2, and NADH is called β-oxidation.
The NADH and FADH2
produced during β-oxidation are used to make ________.
The NADH and FADH2 produced during β-oxidation are used to make ATP by oxidative phosphorylation.
________ is a type of medium used to detect the production of an extracellular protease called caseinase.
Skim milk agar is a type of medium used to detect the production of an extracellular protease called caseinase.
Think about It
- How are the products of lipid and protein degradation connected to glucose metabolism pathways?
- What is the general strategy used by microbes for the degradation of macromolecules?
- Do you think that β-oxidation can occur in an organism incapable of cellular respiration? Why or why not?
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