Microbiology and Immunology

(Axel Boer) #1
WORLD OF MICROBIOLOGY AND IMMUNOLOGY Conjugation

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compost piles are occasionally agitated or “turned over” to
mix the contents, allow oxygen to diffuse throughout the
material (efficient decomposition requires the presence of
oxygen) and to disperse some of the heat. The ideal blend of
microorganisms can be established and maintained by the
addition of waste material to the compost pile so as to not let
the pile become enriched in carbon or nitrogen. A proper ratio
is about 30 parts carbon to one part nitrogen by weight.
Thermophilic bacteria present at this stage of decompo-
sition include Bacillus stearothermophilusand bacteria of the
genus Thermus. A variety of thermophilic fungi are present as
well. These include Rhizomucor pusills, Chaetomium ther-
mophile, Humicola insolens, Humicola lanuginosus, Thermo-
ascus aurabtiacus, and Aspergillus fumigatus.
Thermophilic activity decomposes protein, fat, and car-
bohydrates such as the cellulose that makes up plants and
grass. As this phase of decomposition ends, the temperature
drops and once again the lower-temperature microbes become
dominant. The decomposition of the complex materials by the
thermophilic organisms provides additional nutrients for the
continued decomposition by the mesophilic populations.
Microbiological composting is becoming increasingly
important as space for waste disposal becomes limited. Some
30% of yard and household waste in the United States is
compostable. An average household can decompose about
700 pounds of material per year. If such waste is added to
landfills intact, the subsequent decomposition produces
methane gas and acidic run-off, both of which are environ-
mentally undesirable.

See alsoChemoautotrophic and chemolithotrophic bacteria;
Economic uses and benefits of microorganisms; Soil forma-
tion, involvement of microorganisms

COMPOUND MICROSCOPE•seeMICROSCOPE

AND MICROSCOPY

CONDITIONAL LETHAL MUTANT•see

MICROBIAL GENETICS

CONFIRMED TESTS•seeLABORATORY TECHNIQUES

IN MICROBIOLOGY

CONFOCAL MICROSCOPY•seeMICROSCOPE AND

MICROSCOPY

CConjugationONJUGATION

Conjugation is a mechanism whereby a bacterium can transfer
genetic material to an adjacent bacterium. The genetic transfer
requires contact between the two bacteria. This contact is
mediated by the bacterial appendage called a pilus.
Conjugation allows bacteria to increase their genetic
diversity. Thus, an advantageous genetic trait present in a bac-

terium is capable of transfer to other bacteria. Without conjuga-
tion, the normal bacterial division process does not allow for the
sharing of genetic information and, except for mutationsthat
occur, does not allow for the development of genetic diversity.
A pilus is a hollow tube constructed of a particular pro-
tein. One end is anchored to the surface of a bacterium. The
other end is capable of binding to specific proteins on the sur-
face of another bacterium. A pilus can then act as a portal from
the cytoplasmof one bacterium to the cytoplasm of the other
bacterium. How the underlying membrane layers form chan-
nels to the bacterial cytoplasm is still unclear, although chan-
nel formation may involve what is termed a mating pair
formation (mpf) apparatus on the bacterial surface.
Nonetheless, once a channel has been formed, transfer
of deoxyribonucleic acid (DNA) from one bacterium (the
donor) to the other bacterium (the recipient) can occur.
Conjugation requires a set of F (fertility) genes.
Transfer of DNA from the genome of a bacterium can occur if
the F set of genes is integrated in the bacterial chromosome.
These F genes enter the pilus and literally drag the trailing
genome along behind. Often the pilus will break before the
transfer of the complete genome can occur. Thus, genes that
are located in the vicinity of the F genes will tend to be suc-
cessfully transferred in conjugation more often than genes
located far away from the F genes. This process was originally
discovered in Escherichia coli. Strains that exhibit a higher
than usual tendency to transfer genomic DNA are known as
High Frequency of Recombination(Hfr) strains.
Conjugation also involves transfer of DNA that is
located on a plasmid. A plasmid that contains the F genes is
called the F episome or F plasmid. Other genes on the episome
will be transferred very efficiently, since the entire episome
can typically be transferred before conjugation is terminated
by pilus breakage. If one of the genes codes for a disease caus-
ing factor or antibiotic resistancedeterminant, then episomal
conjugation can be a powerful means of spreading the genetic
trait through a bacterial population. Indeed, conjugation is the
principle means by which bacterial antibiotic resistance is
spread.
Finally, conjugation can involve the transfer of only a
plasmid containing the F genes. This type of conjugation is
also an efficient means of spreading genetic information to
other bacteria. In this case, as more bacteria acquire the F
genes, the proportion of the population that is capable of
genetic transfer via conjugation increases.
Joshua Lederbergdiscovered the process of conjuga-
tion in 1945. He experimented with so-called nutritional
mutants(bacteria that required the addition of a specific nutri-
ent to the growth medium). By incubating the nutritional
mutants in the presence of bacteria that did not require the
nutrient to be added, Lederberg demonstrated that the muta-
tion could be eliminated. Subsequently, another bacteriologist,
William Hayes, demonstrated that the acquisition of genetic
information occurred in a one-way manner (e.g., information
was passing from one bacterium into another), and that the
basis for the information transfer was genetic (i.e., mutants
were isolated in which the transfer did not occur).

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