Encyclopedia of Evolution.pdf - Online Reading Center
Encyclopedia of Evolution.pdf - Online Reading Center
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