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Loline alkaloid

Loline alkaloid is a science topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand Loline alkaloid rather than just read about it. In short: A loline alkaloid is a member of the 1-aminopyrrolizidines (often referred to as lolines), which are bioactive natural products with several distinct biological and chemical features. The lolines are insecticidal and insect-deterrent compounds that are produced in grasses infected by endophytic fungal symbionts of the genus Epichloë (anamorph species: Neotyphodium).

Loline alkaloid — main illustration
Loline alkaloid — illustration

Key takeaways

  • Loline alkaloid belongs to science; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Loline alkaloid to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Loline alkaloid from memory before moving on to harder problems.

Reference excerpt

A loline alkaloid is a member of the 1-aminopyrrolizidines (often referred to as lolines), which are bioactive natural products with several distinct biological and chemical features. The lolines are insecticidal and insect-deterrent compounds that are produced in grasses infected by endophytic fungal symbionts of the genus Epichloë (anamorph species: Neotyphodium). Lolines increase resistance of endophyte-infected grasses to insect herbivores, and may also protect the infected plants from environmental stresses such as drought and spatial competition. They are alkaloids, organic compounds containing basic nitrogen atoms. The basic chemical structure of the lolines comprises a saturated pyrrolizidine ring, a primary amine at the C-1 carbon, and an internal ether bridge—a hallmark feature of the lolines, which is uncommon in organic compounds—joining two distant ring (C-2 and C-7) carbons (see Fig. 1). Different substituents at the C-1 amine, such as methyl, formyl, and acetyl groups, yield loline species that have variable bioactivity against insects. Besides endophyte–grass symbionts, loline alkaloids have also been identified in some other plant species; namely, Adenocarpus species (family Fabaceae) and Argyreia mollis (family Convolvulaceae).

Discovery A member of the loline alkaloids was first isolated from the grass Lolium temulentum and its elemental composition determined in 1892. It was initially named temuline and later renamed norloline. Studies in the 1950s and 1960s by Russian researchers established the name loline and identified the characteristic 2,7 ether bridge in its molecular structure. Since then the analytical methods for purification and analysis of the lolines have been refined and several different loline species have been identified in many Lolium and related grasses infected by the Epichloë/Neotyphodium (epichloae) endophytes. Lolines are absent in grass plants that do not harbor the epichloae endophytes, and not all epichloae produce the lolines. Because of the very intimate association of plant and endophyte and difficulties to reproduce the symbiotic conditions in vitro, it was long unknown if the fungus was the producer of the lolines, or if they were synthesized by the plant in response to endophyte infection. In 2001, it was demonstrated that the endophyte Neotyphodium uncinatum produces lolines in some chemically defined growth media, which suggests that the endophyte is also the producer of the lolines in the grass plant. The lolines have also been reported from some plants in several plant families, suggesting a more widespread occurrence of these compounds in nature.

Mechanism of action Lolines are insecticidal and deterrent to a broad range of insects, including species in the Hemiptera, Coleoptera, Hymenoptera, Lepidoptera, and Blattodea, such as the bird cherry-oat aphid (genus Rhopalosiphum), large milkweed bug (Oncopeltus fasciatus), and American cockroach (Periplaneta americana). LC50 values of N-formylloline or N-acetylloline from grass seed extracts are 1-20 μg/ml for aphids and milkweed bugs and impair insect development and fecundity and cause avoidance of loline-containing grass tissues. However, results of feeding tests with grass extracts are occasionally difficult to interpret due to the presence of other endophyte alkaloids in these extracts, and the exact mechanisms of the insecticidal actions of the lolines are unknown. The lolines may be neurotoxic to the insects, and differences in the chemical groups at the C-1-amine result in different levels of insect toxicity; for example, N-formylloline (see Fig. 2), which occurs in higher concentrations in endophyte-infected grass plants, has greater insect toxicity than some other lolines, which occur at lower concentrations in the grass plant.

Loline bioactivities show some unexpected variability with variation in their concentration in grass tissues. For example, the tall fescue endophyte, N. coenophialum, has been associated with enhanced resistance to the migratory root-endoparasitic nematode, Pratylenchus scribneri. At low concentrations, N-formylloline serves as a chemoattractant for P. scribneri, but acts as a repellant at higher concentrations. However, ergot alkaloids also have repellent and immobilizing effects on P. scribneri, and an endophyte of perennial ryegrass lacking lolines, and genetically engineered to produce no ergot alkaloids, exhibits resistance to this nematode. Therefore, the relative importance of the loline and ergot alkaloids to nematode resistance remains unclear. Many epichloae endophytes—including N. coenophialum symbiotic with Lolium arundinaceum (syn. Festuca arundinacea, tall fescue)—also produce ergot alkaloids that are toxic to mammalian herbivores. The ergot alkaloids occur at relatively low concentrations in the plant and are often difficult to detect analytically. By contrast, the lolines frequently accumulate to very high levels in grass tissues, and were, therefore, initially associated also with toxicity to mammalian herbivores. Specifically, the lolines were thought to be responsible for toxic symptoms called fescue toxicosis displayed by livestock grazing on grasses infected by N. coenophialum. However, subsequently it was demonstrated that only the endophyte-produced ergot alkaloids are responsible for the symptoms of fescue toxicosis (or summer syndrome), and not the lolines which, even at high doses, have only very small physiological effects on mammalians feeders. Another group of alkaloids, the senecio-type alkaloids, are produced by various plants and like the lolines, the senecio alkaloids possess a pyrrolizidine ring structure. Unlike the lolines, however, the senecio alkaloids exhibit strong hepatotoxicity, owing to a double bond between C-1 and C-2 in their ring structure. This double bond is absent in the lolines, explaining the lack of hepatotoxicity of this group of compounds. The lolines have been suggested to inhibit seed germination or growth of other plants (allelopathy), and to increase resistance of infected grasses against drought, but such effects have not been substantiated under more natural conditions of cultivation or in habitats.

Production and distribution in the grass plant

… excerpt ends here. Continue reading the full article.

Illustrations

Loline alkaloid: Figure 1. General structure of the loline alkaloids produced in grasses infected by fungi of the Epichloë/Neotyphodium complex  (epichloae endophytes); R' and R'' denote variable substituents that can include methyl, formyl, and acetyl groups giving rise to different loline species.
Figure 1. General structure of the loline alkaloids produced in grasses infected by fungi of the Epichloë/Neotyphodium complex (epichloae endophytes); R' and R'' denote variable substituents that can include methyl, formyl, and acetyl groups giving rise to different loline species.
Loline alkaloid: Figure 2. N-formylloline, one of the most abundant lolines in endophyte-infected grasses.
Figure 2. N-formylloline, one of the most abundant lolines in endophyte-infected grasses.
Loline alkaloid: Figure 3. Neotyphodium coenophialum hyphae in tall fescue leaf tissue. Lolines commonly accumulate in the N. coenophialum–tall fescue symbiosis, providing protection from insects and other environmental stresses.[1]
Figure 3. Neotyphodium coenophialum hyphae in tall fescue leaf tissue. Lolines commonly accumulate in the N. coenophialum–tall fescue symbiosis, providing protection from insects and other environmental stresses.[1]

Worked examples

Example 1 — a first encounter with Loline alkaloid

Start with the simplest possible case. Write down what Loline alkaloid claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In science, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to Loline alkaloid before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about Loline alkaloid ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of Loline alkaloid

In research
Loline alkaloid appears in science research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses Loline alkaloid in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
Loline alkaloid is common in secondary-school and first-year university syllabi. It links to neighbouring topics Insecticides, Mycotoxins, Pyrrolizidine alkaloids, so understanding it makes those chapters shorter.
In everyday life
Look for Loline alkaloid outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.
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How to study Loline alkaloid in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Loline alkaloid means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain Loline alkaloid out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Loline alkaloid in simple terms?

A loline alkaloid is a member of the 1-aminopyrrolizidines (often referred to as lolines), which are bioactive natural products with several distinct biological and chemical features. The lolines are insecticidal and insect-deterrent compounds that are produced in grasses infected by endophytic fun…

Why does Loline alkaloid matter?

Because it connects several science ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study Loline alkaloid?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on Loline alkaloid.

Tags

  • Insecticides
  • Mycotoxins
  • Pyrrolizidine alkaloids

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