Chapter 28 Protists
Lecture Outline
Overview: A World in a Drop
of Water
·
In
the past, taxonomists classified all protists in a single kingdom, Protista.
·
However,
it is now clear that Protista is in fact paraphyletic.
·
Some
protists are more closely related to plants, fungi, or animals than they are to
other protists.
·
As
a result, the kingdom Protista has been abandoned.
°
Various
lineages are recognized as kingdoms in their own right.
·
Scientists
still use the convenient term protist
informally to refer to eukaryotes that are not plants, animals, or fungi.
Concept 28.1 Protists are an extremely diverse assortment of
eukaryotes
·
Protists
exhibit more structural and functional diversity than any other group of
organisms.
·
Most
protists are unicellular, although there are some colonial and multicellular
ones.
·
At
the cellular level, many protists are very complex.
°
This
is to be expected of a single cell that must carry out the basic functions
performed by all the specialized cells in a multicellular organism.
·
Protists
are the most nutritionally diverse of all eukaryotes.
°
Some
are photoautotrophs, containing chloroplasts.
°
Some
are heterotrophs, absorbing organic molecules or ingesting food particles.
°
Some
are mixotrophs, combining photosynthesis and heterotrophic nutrition.
·
Protists
can be divided into three groups, based on their roles in biological
communities.
°
These
groups are not monophyletic.
°
Protists
include photosynthetic algal protists,
ingestive protozoans, and absorptive
protists.
·
Protist
habitats are also very diverse.
·
The
life cycles of protists vary greatly.
°
Some
are exclusively asexual, while most have life cycles including meiosis and
syngamy.
Endosymbiosis has a place in eukaryotic
evolution.
·
Much
of protist diversity is the result of endosymbiosis, a process in which
unicellular organisms engulfed other cells that evolved into organelles in the
host cell.
·
The
earliest eukaryotes acquired mitochondria by engulfing alpha proteobacteria.
°
The
early origin of mitochondria is supported by the fact that all eukaryotes
studied so far either have mitochondria or had them in the past.
·
Later
in eukaryotic history, one lineage of heterotrophic eukaryotes acquired an
additional endosymbiont—a photosynthetic cyanobacterium—that evolved into
plastids.
°
This
lineage gave rise to red and green algae.
°
This
hypothesis is supported by the observation that the DNA of plastids in red and
green algae closely resembles the DNA of cyanobacteria.
°
Plastids
in these algae are surrounded by two membranes, presumably derived from the cell
membranes of host and endosymbiont.
·
On
several occasions during eukaryotic evolution, red and green algae underwent secondary endosymbiosis.
°
They
were ingested in the food vacuole of a heterotrophic eukaryote and became
endosymbionts themselves.
§
For
example, algae known as chlorarachniophytes evolved when a heterotrophic
eukaryote engulfed a green alga.
§
This
process likely occurred comparatively early in evolutionary time, because the
engulfed alga still carries out photosynthesis with its plastids and contains a
tiny, vestigial nucleus called a nucleomorph.
Concept 28.2 Diplomads and parabasalids have
modified mitochondria
·
Most
diplomonads and parabasalids are found in anaerobic environments.
·
These
protists lack plastids, and their mitochondria lack DNA, an electron transport
chain, and the enzymes needed for the citric acid cycle.
·
In
some species, the mitochondria are very small and produce cofactors for enzymes
involved in ATP production in the cytosol.
·
Diplomonads have two equal-sized
nuclei and multiple flagella.
·
Giardia intestinalis is an infamous diplomonad
parasite that lives in the intestines of mammals.
°
The
most common method of acquiring Giardia
is by drinking water contaminated with feces containing the parasite in a
dormant cyst stage.
·
The
parabasalids include trichomonads.
·
The
best-known species, Trichomonas vaginalis,
inhabits the vagina of human females.
°
If
the normal acidity of the vagina is disturbed, T. vaginalis can outcompete beneficial bacteria and infect the
vaginal lining.
°
The
male urethra may also be infected but without symptoms.
°
The
infection is sexually transmitted.
°
Genetic
studies of T. vaginalis suggest that
the species became pathogenic after some individuals acquired a particular gene
through horizontal gene transfer from other vaginal bacteria.
§
The
gene allows T. vaginalis to feed on
epithelial cells.
Concept 28.3 Euglenozoans have flagella with a
unique internal structure
·
Euglenozoa
is a diverse clade that includes predatory heterotrophs, photosynthetic
autotrophs, and pathogenic parasites.
·
Members
of this group are distinguished by the presence of a spiral or crystalline rod
inside their flagella.
·
Most
euglenozoans have disc-shaped mitochondrial cristae.
·
The
best-studied groups of euglenozoans are the kinetoplastids and euglenids.
·
The
kinetoplastids have a single large
mitochondrion associated with a unique organelle, the kinetoplast.
°
The
kinetoplast houses extranuclear DNA.
°
Kinetoplastids
are symbiotic and include pathogenic parasites.
°
For
example, Trypanosoma causes African
sleeping sickness, a disease spread by the African tsetse fly, and Chagas’
disease, which is transmitted by bloodsucking bugs.
·
Trypanosomes
evade immune detection by switching surface proteins from generation to
generation, preventing the host from developing immunity.
°
One-third
of Trypanosoma’s genome codes for
these surface proteins.
·
Euglenids are characterized by an
anterior pocket from which one or two flagella emerge.
°
They
also have a unique glucose polymer, paramylon, as a storage molecule.
°
Many
species of the euglenid Euglena are
autotrophic but can become heterotrophic in the dark.
°
Other
euglenids can phagocytose prey.
Concept 28.4 Alveolates have sacs beneath the
plasma membrane
·
Members
of the clade Alveolata have alveoli, small membrane-bound cavities, under the
plasma membrane.
°
Their
function is not known, but they may help stabilize the cell surface or regulate
water and ion content.
·
Alveolata
includes flagellated protists (dinoflagellates), parasites (apicomplexans), and
ciliates.
·
Dinoflagellates are abundant components
of marine and freshwater phytoplankton.
°
Dinoflagellates
and other phytoplankton form the foundation of most marine and many freshwater
food chains.
°
Other
species of dinoflagellates are heterotrophic.
°
Most
dinoflagellates are unicellular, but some are colonial.
·
Each
dinoflagellate species has a characteristic shape, often reinforced by internal
plates of cellulose.
·
Two
flagella sit in perpendicular grooves in the “armor” and produce a spinning
movement.
·
Dinoflagellate
blooms, characterized by explosive population growth, can cause “red tides” in
coastal waters.
°
The
blooms are brownish red or pinkish orange because of the presence of
carotenoids in dinoflagellate plasmids.
°
Toxins
produced by some red-tide organisms have produced massive invertebrate and fish
kills.
°
These
toxins can be deadly to humans as well.
·
Some
dinoflagellates form mutualistic symbioses with coral polyps, the animals that
build coral reefs.
°
Photosynthetic
products from the dinoflagellates provide the main food resource for reef
communities.
·
All
apicomplexans are parasites of
animals, and some cause serious human diseases.
°
The
parasites disseminate as tiny infectious cells (sporozoites) with a complex
of organelles specialized for penetrating host cells and tissues at the apex of the sporozoite cell.
°
Apicomplexans
have a nonphotosynthetic plasmid called the apicoplast, which carries out vital
functions including the synthesis of fatty acids.
°
Most
apicomplexans have intricate life cycles with both sexual and asexual stages
and often require two or more different host species for completion.
·
Plasmodium, the parasite that causes
malaria, spends part of its life in mosquitoes and part in humans.
·
The
incidence of malaria was greatly diminished in the 1960s by the use of
insecticides against the Anopheles
mosquitoes, which spread the disease, and by drugs that killed the parasites in
humans.
°
However,
resistant varieties of Anopheles and Plasmodium have caused a malarial
resurgence.
°
About
300 million people are infected with malaria in the tropics, and up to 2
million die each year.
·
The
search for malarial vaccines has had little success because Plasmodium is evasive.
°
It
spends most of its time inside human liver and blood cells, and continually
changes its surface proteins, thereby changing its “face” to the human immune
system.
·
The
need for new treatments for malaria led to a major effort to sequence Plasmodium’s genome.
°
By
2003, researchers had identified the expression of most of the parasite’s genes
at specific points in its life cycle.
°
This
research could help scientists identify potential new targets for vaccines.
°
Identification
of a gene that may confer resistance to chloroquine, an antimalarial drug, may
lead to ways to block drug resistance in Plasmodium.
·
Ciliates are a diverse group of
protists, named for their use of cilia to move and feed.
°
The
cilia may cover the cell surface or be clustered into rows or tufts.
°
Some
ciliates scurry about on leglike structures constructed from many cilia.
°
A
submembrane system of microtubules coordinates ciliary movements.
·
The
cilia are associated with a submembrane system of microtubules that may
coordinate movement.
·
Ciliates
have two types of nuclei, one or more large macronuclei and tiny micronuclei.
°
Each
macronucleus has dozens of copies of the ciliate’s genome.
§
The
genes are not organized into chromosomes but are packaged into small units with
duplicates of a few genes.
§
Macronuclear
genes control the everyday functions of the cell such as feeding, waste
removal, and water balance.
°
Ciliates
generally reproduce asexually by binary fission of the macronucleus, rather
than mitotic division.
·
The
sexual shuffling of genes occurs during conjugation,
during which two individuals exchange haploid micronuclei.
·
In
ciliates, reproduction and conjugation are separate processes.
°
In
a real sense, ciliates have “sex without reproduction.”
·
Conjugation
provides an opportunity for ciliates to eliminate transposons and other types
of “selfish” DNA that can replicate within a genome.
°
During
conjugation, foreign genetic elements are excised when micronuclei develop from
macronuclei.
°
Up
to 15% of a ciliate’s genome may be removed every time it undergoes
conjugation.
Concept 28.5 Stramenopiles have “hairy” and smooth
flagella
·
The
clade Stramenopila includes both
heterotrophic and photosynthetic protists.
°
The
name of this group is derived from the presence of numerous fine, hairlike
projections on the flagella.
§
In
most cases, a “hairy” flagellum is paired with a smooth flagellum.
°
In
most stramenopile groups, the only flagellated stages are motile reproductive
cells.
·
The
heterotrophic stramenopiles, the oomycetes,
include water molds, white rusts,
and downy mildews.
°
Many
oomycetes have multinucleate filaments that resemble fungal hyphae.
°
However,
there are many differences between oomycetes and fungi.
§
Oomycetes
have cell walls made of cellulose, while fungal walls are made of chitin.
§
The
diploid condition, reduced in fungi, is dominant in oomycete life cycles.
§
Oomycetes
have flagellated cells, while almost all fungi lack flagella.
°
Molecular
systematics has confirmed that oomycetes are not closely related to fungi.
§
Their
superficial similarity is a case of convergent evolution.
§
In
both groups, the high surface-to-volume ratio of filamentous hyphae enhances
nutrient uptake.
·
Although
oomycetes descended from photosynthetic ancestors, they no longer have
plastids.
°
Instead,
they acquire nutrients as decomposers or parasites.
·
Water
molds are important decomposers, mainly in fresh water.
°
They
form cottony masses on dead algae and animals.
·
White
rusts and downy mildews are parasites of terrestrial plants.
°
They
are dispersed by windblown spores, and form flagellated zoospores at another
point in their life cycles.
°
One
species of downy mildew threatened French vineyards in the 1870s.
°
Another
species causes late potato blight, which contributed to the Irish famine in the
19th century.
°
Late
blight continues to cause crop losses today.
§
Researchers
are working to develop resistant potatoes by transferring genes from wild potatoes
that confer resistance to blight.
·
Diatoms are unicellular algae
with unique glasslike walls composed of hydrated silica embedded in an organic
matrix.
°
The
wall is divided into two parts that overlap like a shoebox and lid.
°
These
walls allow live diatoms to withstand immense pressure, providing a defense for
them from the crushing jaws of predators.
·
Most
of the year, diatoms reproduce asexually by mitosis with each daughter cell
receiving half of the cell wall and regenerating a new second half.
°
Some
species form cysts as resistant stages.
·
Sexual
stages are not common.
°
When
it occurs, it involves the formation of eggs and amoeboid or flagellated sperm.
·
Diatoms
are a highly diverse group of protists, with an estimated 100,000 species.
·
They
are abundant members of both freshwater and marine plankton.
·
Diatoms
store food reserves as the glucose polymer laminarin or, in a few diatoms, as
oil.
·
Massive
accumulations of fossilized diatoms are major constituents of diatomaceous
earth.
·
Golden algae, or chrysophytes, are
named for their yellow and brown carotenoids.
·
Their
cells are biflagellated, with both flagella attached near one end of the cell.
·
Some
species are mixotrophic, absorbing organic molecules or ingesting bacteria by
phagocytosis.
·
Many
chrysophytes live among freshwater and marine plankton.
°
While
most are unicellular, some are colonial.
°
At
high densities, they can form resistant cysts that remain viable for decades.
·
Brown algae, or phaeophytes, are the
largest and most complex protists known.
°
All
brown algae are multicellular, and most species are marine.
·
Brown
algae are especially common along temperate coasts in areas of cool water and
adequate nutrients.
°
They
owe their characteristic brown or olive color to carotenoids in their plastids,
which are homologous to the plastids of golden algae and diatoms.
·
The
largest marine algae, including brown, red, and green algae, are known
collectively as seaweeds.
·
Seaweeds
inhabit the intertidal and subtidal zones of coastal waters.
°
This
environment is characterized by extreme physical conditions, including wave
forces and exposure to sun and drying conditions at low tide.
·
Seaweeds
have a complex multicellular anatomy, with some differentiated tissues and
organs that resemble those in plants.
°
These
analogous features include the thallus,
or body, of the seaweed.
°
The
thallus typically consists of a rootlike holdfast
and a stemlike stipe, which supports
leaflike photosynthetic blades.
·
The
term “seaweed” refers to brown algae as well as some species of green and red
algae.
·
The
giant seaweeds known as kelps live in deep water beyond the intertidal zone.
°
The
stipes of these algae may be as long as 60 m.
·
Seaweeds
living in the intertidal zone must cope with rough water as well as twice-daily
low tides that expose the algae to hot sun and risk of desiccation.
·
Seaweeds
are important sources of food and commodities.
°
Many
seaweeds are eaten by coastal people, including Laminaria (“kombu” in
°
A
variety of gel-forming substances are extracted in commercial operations.
°
Algin
from brown algae and agar and carrageen from red algae are used as thickeners
in food, lubricants in oil drilling, or culture media in microbiology.
Some algae have life cycles with alternating
multicellular haploid and diploid generations.
·
The
multicellular brown, red, and green algae show complex life cycles with
alternation of multicellular haploid and multicellular diploid forms.
°
A
similar alternation of generations
had a convergent evolution in the life cycle of plants.
·
The
complex life cycle of the kelp Laminaria
provides an example of alternation of generations.
°
The
diploid individual, the sporophyte,
produces haploid spores (zoospores) by meiosis.
°
The
haploid individual, the gametophyte,
produces gametes by mitosis that fuse to form a diploid zygote.
·
In
Laminaria, the sporophyte and
gametophyte are structurally different, or heteromorphic.
·
In
other algae, the alternating generations look alike (isomorphic) but differ in the chromosome number.
Concept 28.6 Cercozoans and radiolarians have
threadlike pseudopodia
·
A
newly recognized clade, Cercozoa, contains the amoebas.
·
The
term “amoeba” used to refer to protists that move and feed by means of pseudopodia, cellular extensions that
bulge from the cell surface.
·
When
an amoeba moves, it extends a pseudopodium and anchors the tip.
·
Cytoplasm
then streams into the pseudopodium.
·
It
is now clear that amoebas are not a monophyletic group.
·
Those
that belong to the clade Cercozoa are distinguished by their threadlike
pseudopodia.
·
Cercozoans
include chlorarachniophytes and foraminiferans and are closely related to
radiolarians, which also have threadlike pseudopodia.
·
Foraminiferans, or forams, are named for their porous shells, or tests.
·
Forams
have multichambered, porous shells, consisting of organic materials hardened
with calcium carbonate.
°
Pseudopodia
extend through the pores for swimming, shell formation, and feeding.
°
Many
forams form symbioses with algae.
·
Forams
live in marine and fresh water.
°
Most
live in sand or attach to rocks or algae.
°
Some
are abundant in the plankton.
·
More
than 90% of the described forams are fossils.
°
The
calcareous skeletons of forams are important components of marine sediments.
°
Fossil
forams are often used as chronological markers to correlate the ages of
sedimentary rocks from different parts of the world.
·
Radiolarians are mostly marine
protists whose siliceous skeletons are fused into one delicate piece.
·
Pseudopodia
known as axopodia radiate from the central body and are reinforced by
microtubules.
·
The
microtubules are covered by a thin layer of cytoplasm, which phagocytoses
organisms that become attached to the axopodia.
·
After
death, radiolarian tests accumulate as an ooze that may be hundreds of meters
thick in some seafloor locations.
Concept 28.7 Amoebozoans have lobe-shaped
pseudopodia
·
Many
species of amoebas that have lobe-shaped pseudopodia belong to the clade
Amoebozoans, which includes gymnamoebas, entamoebas, and slime molds.
·
Gymnamoebas are a large and varied
group of Amoebozoans.
·
They
are common in soil as well as freshwater and marine environments.
·
Most
are heterotrophs that actively seek and consume bacteria and protists, while
some feed on detritus.
·
Entamoebas include free-living and
parasitic species.
·
Humans
host at least six species of Entamoeba.
°
One,
E. histolytica, causes amebic
dysentery, spread through contaminated drinking water and food.
°
This
disease kills 100,000 people each year.
·
Slime molds were once thought to be
fungi because they produce fruiting bodies that disperse their spores.
°
However,
this resemblance is due to evolutionary convergence.
·
Molecular
systematics places slime molds in the clade Amoebozoa and suggests that they
descended from unicellular, gymnamoeba-like ancestors.
·
Slime
molds have diverged into two lineages with distinctive life cycles: plasmodial
slime molds and cellular slime molds.
·
The
plasmodial slime molds are brightly
pigmented, heterotrophic organisms.
·
The
feeding stage is an amoeboid mass, the plasmodium,
which may be several centimeters in diameter.
°
The
plasmodium is not multicellular, but rather a single mass of cytoplasm with
multiple diploid nuclei.
°
The
diploid nuclei undergo synchronous mitotic divisions, thousands at a time.
°
Because
of this characteristic, plasmodial slime molds have been used for studies of
the molecular details of the cell cycle.
·
Within
the cytoplasm, cytoplasmic streaming distributes nutrients and oxygen
throughout the plasmodium.
·
The
plasmodium phagocytoses food particles from moist soil, leaf mulch, or rotting
logs.
·
If
the habitat begins to dry or if food levels drop, the plasmodium stops growing
and differentiates into a stage of the life cycle that produces fruiting
bodies, which function in sexual reproduction.
·
Plasmodial
slime molds are primarily diploid.
·
Cellular slime molds straddle the line between
individuality and multicellularity.
°
The
feeding stage consists of solitary cells that feed and divide mitotically as
individuals.
°
When
food is scarce, the cells form an aggregate (“slug”) that functions as a unit.
§
Each
cell retains its identity in the aggregate.
·
The
dominant stage in a cellular slime mold is the haploid stage.
·
Most
cellular slime molds lack flagellated stages.
·
Dictyostelium discoideum is a common cellular
slime mold that has become a model organism for addressing the evolution of
multicellularity.
·
As
the fruiting body forms, cells that form the stalk dry out and die, cells at
the top survive, form spores, and have the potential for future reproduction.
°
Scientists
have found that mutations to a single gene can turn individual Dictyostelium cells into “cheaters” that
never become part of the stalk.
°
Since
these mutants gain a strong reproductive advantage over noncheaters, why do all
Dictyostelium cells not cheat?
·
A
group of scientists recently found a possible answer to this puzzle.
°
Cheating
mutants lack a protein on their cell surface, and noncheating cells can
recognize this difference.
°
Noncheaters
preferentially aggregate with other noncheaters, depriving cheaters of the
opportunity to exploit them.
·
Such
recognition systems may have been important in the evolution of multicellular
animals and plants.
Concept 28.8 Red algae and green algae are the
closest relatives of land plants
·
More
than a billion years ago, a heterotrophic protist acquired a cyanobacterial
endosymbiont.
°
The
photosynthetic descendents of this ancient protist evolved into the red and
green algae.
·
At
least 475 million years ago, the lineage that produced green algae gave rise to
the land plants.
·
Unlike
other eukaryotic algae, red algae
have no flagellated stages in their life cycle.
·
There
are more than 6,000 known species of red algae, which are reddish due to the
accessory pigment phycoerythrin.
°
Coloration
varies among species and depends on the depth that they inhabit.
°
Some
species lack pigmentation and are parasites on other red algae.
·
Red
algae are the most common seaweeds in the warm coastal waters of tropical
oceans.
°
Red
algae inhabit deeper waters than other photosynthetic eukaryotes.
°
Their
photosynthetic pigments, especially phycobilins, allow them to absorb blue and
green wavelengths that penetrate down to deep water.
°
One
red algal species has been discovered off the
·
Some
red algae live in fresh water or on land.
·
Most
red algae are multicellular, with some reaching a size large enough to be
called “seaweeds.”
°
The
thalli of many red algal species are filamentous.
°
The
base of the thallus is usually differentiated into a simple holdfast.
·
The
life cycles of red algae are especially diverse.
°
In
the absence of flagella, fertilization depends entirely on water currents to
bring gametes together.
°
Alternation
of generations is common in red algae.
·
Green algae are named for their
grass-green chloroplasts.
°
These
are similar in ultrastructure and pigment composition to those of plants.
·
Molecular
systematics and cellular morphology provide considerable evidence that green
algae and land plants are closely related.
°
In
fact, some systematists advocate the inclusion of green algae into an expanded
“plant” kingdom, Viridiplantae.
·
Green
algae are divided into two main groups, chlorophytes and charophyceans.
·
Most
of the 7,000 species of chlorophytes have been identified.
°
Most
live in fresh water, but many are marine inhabitants.
°
Some
chlorophytes inhabit damp soil, while others are specialized to live on
glaciers and snowfields.
§
These
snow-dwelling chlorophytes carry out photosynthesis despite subfreezing
temperatures and intense visible and ultraviolet radiation.
§
They
are protected by radiation-blocking compounds in their cytoplasm and by the
snow itself, which acts as a shield.
°
Some
chlorophytes live symbiotically with fungi to form lichens, a mutualistic collective.
·
Large
size and complexity in chlorophytes has evolved by three different mechanisms:
1. Formation of colonies of
individual cells (e.g., Volvox).
2. The repeated division of
nuclei without cytoplasmic division to form multinucleate filaments (e.g.,
Caulerpa).
3. The formation of true
multicellular forms by cell division and cell differentiation (e.g., Ulva).
·
Some
multicellular marine chlorophytes are large and complex enough to qualify as
seaweeds.
·
Most
green algae have complex life cycles, with both sexual and asexual reproductive
stages.
°
Most
sexual species have biflagellated gametes with cup-shaped chloroplasts.
°
Alternation
of generations evolved in the life cycles of some green algae.
·
The
other main group of green algae is most closely related to land plants.