Elaioplasts are one of the three possible forms of leucoplasts, sometimes broadly referred to as such. [1] The main function of elaioplasts are synthesis and storage of fatty acids, terpenes, and other lipids, and they can be found in the embryonic leaves of oilseeds, citrus fruits, as well as the anthers of many flowering plants. [1] [2] [3] [4]
Like most leucoplasts, elaioplasts are non-pigmented organelles capable of alternating between the different forms of plastids. The elaioplast specifically is primarily responsible for the storage and metabolism of lipids, [5] among these roles, recent studies have shown that these organelles participate in the formation of terpenes and fatty acids. [2] [3] Typically, they appear as small, rounded organelles filled by oil droplets. [1] Lipids found inside elaioplasts mirror those synthesized by prokaryotes, chiefly triacylglycerol and sterol esters, which cluster into the droplets visible by microscope. [1] As for their other components, elaioplasts also contain plastoglobuli associated proteins such as fibrillins, a protein family believed to be retained from the cyanobacterial ancestors of plastids. [4] Alongside the tapetosomes (clusters of oil and proteins produced by the endoplasmic reticulum), elaioplasts are frequently found in the tapetum of angiosperm anthers, where their products, oil from the plastid and protein from the tapetosome, are used to form the pollen coat of developing grains. [1] Following the maturation of pollen grains, these organelles are degraded and released into the anther loculus. [1] Found also in oilseeds, elaioplasts in this group provide lipids to be converted into carbohydrates which will serve as fuel in the embryo's germination. [4] Citrus specimens have been shown to have especially high amounts of elaioplasts in their fruit peels, where they are essential to the production of terpenes. [5]
Within the plant, elaioplasts, as well as all other plastids, arise from proplastids in the dividing portion of the stem (meristem). These proplastids have not yet differentiated and, as such, can develop into any variety of known plastids, determined by the tissues they are present in. [6] In vegetative cells, proplastids usually follow a unidirectional pathway of development with no reversals between one form and the next. Reproductive cells, however, may have plastids that inter-convert frequently. [7] In the anthers of flowering plants, elaioplasts represent the final stage of plastid development within the tapetum, either emerging directly from proplastids or the conversion of other plastids, depending on the species and pollination strategy. [7]
Plastids are hypothesized to have originated with an endosymbiotic event between an ancient eukaryote and cyanobacterial ancestor more than 1 billion years ago, where the bacteria was engulfed by the other and retained where it served as the metabolic center for photosynthesis. [8] Evidence of this can be observed today in the independent genomes characteristic of plastids, found to be closely related to modern cyanobacteria. [9] Since their ancient symbiotic event, the plastid genome has been reduced significantly, with the organelles themselves coding for around 100 of the 2500 associated proteins, everything else being transferred to the nuclear genome. [1]
Like most plastids, elaioplasts reproduce through binary fission independent from the division of the parent cell, a feature indicative of their bacterial ancestry. [1] This fission occurs just before cytokinesis, with the products then being transported to the daughter cells as a component of the cytoplasm. [1]
As a result of the ability to inter-convert between other types of the plastid family, elaioplasts share the same plastome (plastid genome) with all other plastids and are predominately inherited maternally in angiosperms. [5] [7] As its name implies, maternal inheritance excludes the plastome of the father through one of two ways: during pollen development or in pollen tube formation. [7] During pollen development, paternal plastids are halted by microfilaments in the cytoskeleton just prior to microspore division or degeneration just after. [7] Paternal plastome contribution can also be prevented during pollen tube formation, where the plastids are separated from sperm cells as they fuse with the egg. [7]
In cell biology, the cytoplasm describes all material within a eukaryotic cell, enclosed by the cell membrane, except for the cell nucleus. The material inside the nucleus and contained within the nuclear membrane is termed the nucleoplasm. The main components of the cytoplasm are the cytosol, the organelles, and various cytoplasmic inclusions. The cytoplasm is about 80% water and is usually colorless.
A chloroplast is a type of membrane-bound organelle known as a plastid that conducts photosynthesis mostly in plant and algal cells. The photosynthetic pigment chlorophyll captures the energy from sunlight, converts it, and stores it in the energy-storage molecules ATP and NADPH while freeing oxygen from water in the cells. The ATP and NADPH is then used to make organic molecules from carbon dioxide in a process known as the Calvin cycle. Chloroplasts carry out a number of other functions, including fatty acid synthesis, amino acid synthesis, and the immune response in plants. The number of chloroplasts per cell varies from one, in unicellular algae, up to 100 in plants like Arabidopsis and wheat.
Plant cells are the cells present in green plants, photosynthetic eukaryotes of the kingdom Plantae. Their distinctive features include primary cell walls containing cellulose, hemicelluloses and pectin, the presence of plastids with the capability to perform photosynthesis and store starch, a large vacuole that regulates turgor pressure, the absence of flagella or centrioles, except in the gametes, and a unique method of cell division involving the formation of a cell plate or phragmoplast that separates the new daughter cells.
Symbiogenesis is the leading evolutionary theory of the origin of eukaryotic cells from prokaryotic organisms. The theory holds that mitochondria, plastids such as chloroplasts, and possibly other organelles of eukaryotic cells are descended from formerly free-living prokaryotes taken one inside the other in endosymbiosis. Mitochondria appear to be phylogenetically related to Rickettsiales bacteria, while chloroplasts are thought to be related to cyanobacteria.
The plastid is a membrane-bound organelle found in the cells of plants, algae, and some other eukaryotic organisms. They are considered to be intracellular endosymbiotic cyanobacteria. Examples include chloroplasts, chromoplasts, and leucoplasts.
Thylakoids are membrane-bound compartments inside chloroplasts and cyanobacteria. They are the site of the light-dependent reactions of photosynthesis. Thylakoids consist of a thylakoid membrane surrounding a thylakoid lumen. Chloroplast thylakoids frequently form stacks of disks referred to as grana. Grana are connected by intergranal or stromal thylakoids, which join granum stacks together as a single functional compartment.
Chloroplasts contain several important membranes, vital for their function. Like mitochondria, chloroplasts have a double-membrane envelope, called the chloroplast envelope, but unlike mitochondria, chloroplasts also have internal membrane structures called thylakoids. Furthermore, one or two additional membranes may enclose chloroplasts in organisms that underwent secondary endosymbiosis, such as the euglenids and chlorarachniophytes.
Leucoplasts are a category of plastid and as such are organelles found in plant cells. They are non-pigmented, in contrast to other plastids such as the chloroplast.
Chromoplasts are plastids, heterogeneous organelles responsible for pigment synthesis and storage in specific photosynthetic eukaryotes. It is thought that like all other plastids including chloroplasts and leucoplasts they are descended from symbiotic prokaryotes.
A stromule is a microscopic structure found in plant cells. Stromules are highly dynamic structures extending from the surface of all plastid types, including proplastids, chloroplasts, etioplasts, leucoplasts, amyloplasts, and chromoplasts. Protrusions from and interconnections between plastids were observed in 1888 and 1908 and have been described sporadically in the literature since then. Stromules were recently rediscovered in 1997 and have since been reported to exist in a number of angiosperm species including Arabidopsis thaliana, wheat, rice and tomato, but their role is not yet fully understood.
A nuclear gene is a gene that has its DNA nucleotide sequence physically situated within the cell nucleus of a eukaryotic organism. This term is employed to differentiate nuclear genes, which are located in the cell nucleus, from genes that are found in mitochondria or chloroplasts. The vast majority of genes in eukaryotes are nuclear.
Proteinoplasts are specialized organelles found only in plant cells. Proteinoplasts belong to a broad category of organelles known as plastids. Plastids are specialized double-membrane organelles found in plant cells. Plastids perform a variety of functions such as metabolism of energy, and biological reactions. There are multiple types of plastids recognized including Leucoplasts, Chromoplasts, and Chloroplasts. Plastids are broken up into different categories based on characteristics such as size, function and physical traits. Chromoplasts help to synthesize and store large amounts of carotenoids. Chloroplasts are photosynthesizing structures that help to make light energy for the plant. Leucoplasts are a colorless type of plastid which means that no photosynthesis occurs here. The colorless pigmentation of the leucoplast is due to not containing the structural components of thylakoids unlike what is found in chloroplasts and chromoplasts that gives them their pigmentation. From leucoplasts stems the subtype, proteinoplasts, which contain proteins for storage. They contain crystalline bodies of protein and can be the sites of enzyme activity involving those proteins. Proteinoplasts are found in many seeds, such as brazil nuts, peanuts and pulses. Although all plastids contain high concentrations of protein, proteinoplasts were identified in the 1960s and 1970s as having large protein inclusions that are visible with both light microscopes and electron microscopes. Other subtypes of Leucoplasts include amyloplast, and elaioplasts. Amyloplasts help to store and synthesize starch molecules found in plants, while elaioplasts synthesize and store lipids in plant cells.
An apicoplast is a derived non-photosynthetic plastid found in most Apicomplexa, including Toxoplasma gondii, and Plasmodium falciparum and other Plasmodium spp., but not in others such as Cryptosporidium. It originated from algae through secondary endosymbiosis; there is debate as to whether this was a green or red alga. The apicoplast is surrounded by four membranes within the outermost part of the endomembrane system. The apicoplast hosts important metabolic pathways like fatty acid synthesis, isoprenoid precursor synthesis and parts of the heme biosynthetic pathway.
A transplastomic plant is a genetically modified plant in which genes are inactivated, modified or new foreign genes are inserted into the DNA of plastids like the chloroplast instead of nuclear DNA.
The CoRR hypothesis states that the location of genetic information in cytoplasmic organelles permits regulation of its expression by the reduction-oxidation ("redox") state of its gene products.
Chloroplast DNA (cpDNA) is the DNA located in chloroplasts, which are photosynthetic organelles located within the cells of some eukaryotic organisms. Chloroplasts, like other types of plastid, contain a genome separate from that in the cell nucleus. The existence of chloroplast DNA was identified biochemically in 1959, and confirmed by electron microscopy in 1962. The discoveries that the chloroplast contains ribosomes and performs protein synthesis revealed that the chloroplast is genetically semi-autonomous. The first complete chloroplast genome sequences were published in 1986, Nicotiana tabacum (tobacco) by Sugiura and colleagues and Marchantia polymorpha (liverwort) by Ozeki et al. Since then, a great number of chloroplast DNAs from various species have been sequenced.
Cyanidioschyzon merolae is a small (2μm), club-shaped, unicellular haploid red alga adapted to high sulfur acidic hot spring environments. The cellular architecture of C. merolae is extremely simple, containing only a single chloroplast and a single mitochondrion and lacking a vacuole and cell wall. In addition, the cellular and organelle divisions can be synchronized. For these reasons, C. merolae is considered an excellent model system for study of cellular and organelle division processes, as well as biochemistry and structural biology. The organism's genome was the first full algal genome to be sequenced in 2004; its plastid was sequenced in 2000 and 2003, and its mitochondrion in 1998. The organism has been considered the simplest of eukaryotic cells for its minimalist cellular organization.
A plastid is a membrane-bound organelle found in plants, algae and other eukaryotic organisms that contribute to the production of pigment molecules. Most plastids are photosynthetic, thus leading to color production and energy storage or production. There are many types of plastids in plants alone, but all plastids can be separated based on the number of times they have undergone endosymbiotic events. Currently there are three types of plastids; primary, secondary and tertiary. Endosymbiosis is reputed to have led to the evolution of eukaryotic organisms today, although the timeline is highly debated.
Christoph Benning is a German–American plant biologist. He is an MSU Foundation Professor and University Distinguished Professor at Michigan State University. Benning's research into lipid metabolism in plants, algae and photosynthetic bacteria, led him to be named Editor-in-Chief of The Plant Journal in October 2008.