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Encyclopedia of Evolution.pdf - Online Reading Center

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0 respiration, evolution <strong>of</strong><br />

There is some concern that the genetic basis <strong>of</strong> herbicide<br />

resistance, which has been put into crops by genetic engineering,<br />

could spread to wild weed species by crossbreeding (see<br />

hybridization). While this has not happened extensively, it<br />

has occurred: Herbicide resistance has been transferred from<br />

crops to weeds within the crucifer (mustard) family by crosspollination.<br />

Once the resistance genes are in the wild weed<br />

populations, natural selection will favor their spread whenever<br />

herbicides are used.<br />

An evolutionary understanding <strong>of</strong> medicine, public<br />

health, and agriculture demands that antibiotics, pesticides,<br />

and herbicides be used sparingly in order to minimize environmental<br />

contamination and to prevent the evolution <strong>of</strong><br />

resistance in the very species <strong>of</strong> organisms humans are trying<br />

to control. By restraining the use <strong>of</strong> chemical control agents,<br />

they will remain effective when they are really needed in an<br />

emergency.<br />

The dangerous emergence <strong>of</strong> bacteria, pests, and weeds<br />

that resist the chemicals that we use to control them has<br />

resulted from our overuse <strong>of</strong> chemical control agents. The<br />

overuse <strong>of</strong> antibiotics, pesticides, and herbicides resulted<br />

not only from overlooking the laws <strong>of</strong> ecology but also<br />

the laws <strong>of</strong> evolution. As noted in the Introduction to this<br />

encyclopedia, “what you don’t know about evolution can<br />

kill you.”<br />

Further <strong>Reading</strong><br />

Amábile-Cuevas, Carlos F. “New antibiotics and new resistance.”<br />

American Scientist 91 (2003): 138–149.<br />

Brookfield, J. F. Y. “The resistance movement.” Nature 350 (1991):<br />

107–108.<br />

Carson, Rachel. Silent Spring. New York: Houghton Mifflin, 1962.<br />

Department <strong>of</strong> Health and Human Services, Washington, D.C. “<strong>Center</strong>s<br />

for Disease Control and Prevention.” Available online. URL:<br />

http://www.cdc.gov. Accessed May 4, 2005.<br />

Enright, Mark C. “The evolutionary history <strong>of</strong> methicillin-resistant<br />

Staphylococcus aureus (MRSA). Proceedings <strong>of</strong> the National<br />

Academy <strong>of</strong> Sciences 99 (2002): 7,687–7,692.<br />

Hegde, Subray S., et al. “A fluoroquinolone resistance protein from<br />

Mycobacterium tuberculosis that mimics DNA.” Science 308<br />

(2005): 1,480–1,483. Summarized by Ferber, Dan. “Protein that<br />

mimics DNA helps tuberculosis bacteria resist antibiotics.” Science<br />

308 (2005): 1,393.<br />

Levy, Stuart B. “The challenge <strong>of</strong> antibiotic resistance.” Scientific<br />

American, March 1998, 32–39.<br />

Monnet, Dominique L., et al. “Antimicrobial drug use and methicillin-resistant<br />

Staphylococcus aureus, Aberdeen, 1996–2000.”<br />

Emerging Infectious Diseases 10 (2004): 1,432–1,441. Available<br />

online. URL: http://www.cdc.gov/ncidod/eid/vol10no8/02-0694.<br />

htm. Accessed May 4, 2005.<br />

Regoes, Roland R., and Sebastian Bonhoeffer. “Emergence <strong>of</strong> drugresistant<br />

influenza virus: Population dynamical considerations.”<br />

Science 312 (2006): 389–391.<br />

Smith, P., et al. “A new aspect <strong>of</strong> warfarin resistance in wild rats:<br />

Benefits in the absence <strong>of</strong> poison.” Functional Ecology 7 (1993):<br />

190–194.<br />

Stix, Gary. “An antibiotic resistance fighter.” Scientific American,<br />

April 2006, 80–83.<br />

Tiemersma, Edine W., et al. “Methicillin-resistant Staphylococcus<br />

aureus in Europe, 1999–2002. Emerging Infectious Diseases 10<br />

(2004): 1,627–1,634. Available online. URL: http://www.cdc.gov/<br />

ncidod/EID/vol10no9/04-0069.htm. Accessed May 4, 2005.<br />

WeedScience.org. “International Survey <strong>of</strong> Herbicide Resistant<br />

Weeds.” Available online. URL: http://www.weedscience.org/<br />

in.asp. Accessed May 4, 2005.<br />

Wenzel, Richard P., and Michael B. Edmond. “The impact <strong>of</strong> hospital-acquired<br />

bloodstream infections.” Emerging Infectious Diseases<br />

7 (2001): 174–177. Available online. URL: http://www.cdc.<br />

gov/ncidod/eid/vol7no2/wenzel.htm. Accessed October 7, 2005.<br />

respiration, evolution <strong>of</strong> Respiration is the process by<br />

which cells transfer energy from food molecules to ATP.<br />

ATP (adenosine triphosphate) is almost universally used as<br />

the molecule that puts energy directly into enzyme reactions.<br />

And since almost all biological reactions are controlled by<br />

enzymes, ATP is called the “energy currency <strong>of</strong> the cell.” Cellular<br />

respiration, which produces ATP, occurs in many bacteria<br />

(see bacteria, evolution <strong>of</strong>), and in the cytoplasm<br />

and mitochondria <strong>of</strong> eukaryotic cells (see eukaryotes, evolution<br />

<strong>of</strong>). Food molecules store energy over relatively long<br />

time periods, while ATP puts energy to immediate use. Therefore<br />

mitochondria are like power plants, which transfer the<br />

energy from long-term storage (coal, natural gas) into immediately<br />

available forms like electricity.<br />

The earliest bacteria, during the Archaean eon (see Precambrian<br />

time), were anaerobic: not only was there no oxygen<br />

gas in the environment, but oxygen gas would have been<br />

deadly to them. Their descendants are the anaerobic bacteria<br />

that today can only live in mud and in the intestines <strong>of</strong> animals.<br />

These bacteria, as well as a few anaerobic protists and<br />

invertebrates (see invertebrates, evolution <strong>of</strong>), use a set <strong>of</strong><br />

reactions called glycolysis to break down glucose sugar molecules<br />

and release some energy from them into ATP. In these<br />

organisms, glycolysis is followed by fermentation. In some<br />

cases, as with yeasts, fermentation produces ethyl alcohol (ethanol);<br />

in other cases, as with Lactobacillus bacteria that make<br />

milk into yogurt, fermentation produces lactic acid (lactate). In<br />

some cases, the cells <strong>of</strong> organisms that rely upon oxygen can<br />

revert temporarily to a dependence on glycolysis and fermentation,<br />

when oxygen is not available. Muscle cells, for example,<br />

can revert to fermentation when they work so fast that the<br />

blood cannot supply sufficient oxygen to them. Muscle pain<br />

results from the buildup <strong>of</strong> lactate, and the muscles develop<br />

an oxygen debt. The muscles stop working after a few minutes<br />

<strong>of</strong> emergency oxygen debt. Ethanol and lactate, however, still<br />

contain most <strong>of</strong> the energy that was in the original glucose.<br />

During the Proterozoic era <strong>of</strong> the Precambrian, cyanobacteria<br />

began producing oxygen gas, which gradually accumulated<br />

to become abundant in the oceans and atmosphere<br />

(see photosynthesis, evolution <strong>of</strong>). This was a crisis for<br />

anaerobic bacteria, which could survive only in the places<br />

where they are found today. However, at this time, some<br />

bacteria evolved a set <strong>of</strong> reactions (aerobic respiration) that<br />

not only tolerated oxygen gas but actually made use <strong>of</strong> it.<br />

A cycle <strong>of</strong> chemical reactions (the Krebs cycle or citric acid<br />

cycle) breaks down the product <strong>of</strong> glycolysis into carbon

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