Protochlorophyllide

Last updated
Protochlorophyllide
Protochlorophyllide a.png
Names
IUPAC name
Magnesium (21R)-3-(2-carboxyethyl)-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxo-9-vinyl-3,4,23,25-tetradehydrophorbine-23,25-diide
Other names
Monovinyl protochlorophyllide
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
PubChem CID
  • InChI=1S/C35H34N4O5.Mg/c1-8-19-15(3)22-12-24-17(5)21(10-11-28(40)41)32(38-24)30-31(35(43)44-7)34(42)29-18(6)25(39-33(29)30)14-27-20(9-2)16(4)23(37-27)13-26(19)36-22;/h8,12-14,31H,1,9-11H2,2-7H3,(H3,36,37,38,39,40,41,42);/q;+2/p-2/t31-;/m1./s1
    Key: QBPCOMNNISRCTC-JSSVAETHSA-L
  • CCC1=C(C)C2=[N+]3C1=Cc1c(C)c4C(=O)[C@H](C(=O)OC)C5=C6C(CCC(O)=O)=C(C)C7=[N+]6[Mg--]3(n1c45)n1c(=C7)c(C)c(C=C)c1=C2
Properties
C35H32MgN4O5
Molar mass 612.957 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
The Arabidopsis mutant (FLU), unable to control biosynthesis of protochlorophyllide, glows red in the blue light. Flumutant.png
The Arabidopsis mutant (FLU), unable to control biosynthesis of protochlorophyllide, glows red in the blue light.

Protochlorophyllide, [1] or monovinyl protochlorophyllide, is an intermediate in the biosynthesis of chlorophyll a. It lacks the phytol side-chain of chlorophyll and the reduced pyrrole in ring D. [2] Protochlorophyllide is highly fluorescent; mutants that accumulate it glow red if irradiated with blue light. [3] In angiosperms, the later steps which convert protochlorophyllide to chlorophyll are light-dependent, and such plants are pale (chlorotic) if grown in the darkness. Gymnosperms, algae, and photosynthetic bacteria have another, light-independent enzyme and grow green in the darkness as well.

Contents

Conversion to chlorophyll

The enzyme that converts protochlorophyllide to chlorophyllide a, the next intermediate on the biosynthetic pathway, [4] is protochlorophyllide reductase, [5] EC 1.3.1.33. There are two structurally unrelated proteins with this activity: the light-dependent and the dark-operative. The light-dependent reductase needs light to operate. The dark-operative version is a completely different protein, consisting of three subunits that exhibit significant sequence similarity to the three subunits of nitrogenase, which catalyzes the formation of ammonia from dinitrogen. [6] This enzyme might be evolutionary older but (being similar to nitrogenase) is highly sensitive to free oxygen and does not work if its concentration exceeds about 3%. [7] Hence, the alternative, light-dependent version needed to evolve.

Most of the photosynthetic bacteria have both light-dependent and light-independent reductases. Angiosperms have lost the dark-operative form and rely on 3 slightly different copies of light-dependent version, frequently abbreviated as POR A, B, and C. Gymnosperms have much more copies of the similar gene (Loblolly pine has about 11 Loblolly Pine (Pinus taeda L.) Contains Multiple Expressed Genes Encoding Light-Dependent NADPH:Protochlorophyllide Oxidoreductase (POR)). In plants, POR is encoded in the cell nucleus and only later transported to its place of work, chloroplast. Unlike with POR, in plants and algae that have the dark-operative enzyme it is at least partially encoded in the chloroplast genome. [8]

Potential danger for plant

Chlorophyll itself is bound to proteins and can transfer the absorbed energy in the required direction. Protochlorophyllide, however, occurs mostly in the free form and, under light conditions, acts as a photosensitizer, forming highly toxic free radicals. Hence, plants need an efficient mechanism of regulating the amount of chlorophyll precursor. In angiosperms, this is done at the step of δ-aminolevulinic acid (ALA), one of the intermediate compounds in the biosynthetic pathway. Plants that are fed by ALA accumulate high and toxic levels of protochlorophyllide, as do mutants with a disrupted regulatory system.

ArabidopsisFLU mutant with damaged regulation can survive only either in a continuous darkness (protochlorophyllide is not dangerous in the darkness) or under continuous light, when the plant is can convert all produced protochlorophyllide into chlorophyll and does not over accumulate it despite the lack of regulation. In barley Tigrina mutant (mutated on the same gene, [9] ) light kills the majority of the leaf tissue that has developed in the darkness, but part of the leaf that originated during the day survives. As a result, the leaves are covered by white stripes of necrotic regions, and the number of the white stripes is close to the age of the leaf in days. Green regions survive the subsequent nights, likely because the synthesis of chlorophyll in the mature leaf tissue is greatly reduced anyway.

Biosynthesis regulatory protein FLU

In spite of numerous past attempts to find the mutant that overacumulates protochlorophyllide under usual conditions, only one such gene (flu) is currently (2009) known. Flu (first described in [3] ) is a nuclear-encoded, chloroplast-located protein that appears containing only protein-protein interaction sites. It is currently not known which other proteins interact through this linker. The regulatory protein is a transmembrane protein that is located in the thylakoid membrane. Later, it was discovered that Tigrina mutants in barley, known a long time ago, are also mutated in the same gene. [9] It is not obvious why no mutants of any other gene were observed; maybe mutations in other proteins, involved into the regulatory chain, are fatal. Flu is a single gene, not a member of the gene family.

Later, by the sequence similarity, a similar protein was found in Chlamydomonas algae, [10] showing that this regulatory subsystem existed a long time before the angiosperms lost the independent conversion enzyme. In a different manner, the Chlamydomonas regulatory protein is more complex: It is larger, crosses the thylakoid membrane twice rather than once, contains more protein-protein interactions sites, and even undergoes alternative splicing. It appears that the regulatory system underwent simplification during evolution.

Related Research Articles

<span class="mw-page-title-main">Chloroplast</span> Plant organelle that conducts photosynthesis

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.

<span class="mw-page-title-main">Chlorophyll</span> Green pigments found in plants, algae and bacteria

Chlorophyll is any of several related green pigments found in cyanobacteria and in the chloroplasts of algae and plants. Its name is derived from the Greek words χλωρός, khloros and φύλλον, phyllon ("leaf"). Chlorophyll allow plants to absorb energy from light.

<i>Chlamydomonas</i> Genus of algae

Chlamydomonas is a genus of green algae consisting of about 150 species of unicellular flagellates, found in stagnant water and on damp soil, in freshwater, seawater, and even in snow as "snow algae". Chlamydomonas is used as a model organism for molecular biology, especially studies of flagellar motility and chloroplast dynamics, biogenesis, and genetics. One of the many striking features of Chlamydomonas is that it contains ion channels (channelrhodopsins) that are directly activated by light. Some regulatory systems of Chlamydomonas are more complex than their homologs in Gymnosperms, with evolutionarily related regulatory proteins being larger and containing additional domains.

<span class="mw-page-title-main">Thylakoid</span> Membrane enclosed compartments in chloroplasts and cyanobacteria

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.

<span class="mw-page-title-main">RuBisCO</span> Key enzyme of the photosynthesis involved in carbon fixation

Ribulose-1,5-bisphosphate carboxylase/oxygenase, commonly known by the abbreviations RuBisCo, rubisco, RuBPCase, or RuBPco, is an enzyme involved in light-independent part of photosynthesis, including the carbon fixation by which atmospheric carbon dioxide is converted by plants and other photosynthetic organisms to energy-rich molecules such as glucose. It emerged approximately four billion years ago in primordial metabolism prior to the presence of oxygen on earth. It is probably the most abundant enzyme on Earth. In chemical terms, it catalyzes the carboxylation of ribulose-1,5-bisphosphate.

<span class="mw-page-title-main">Pyrenoid</span> Organelle found within the chloroplasts of algae and hornworts

Pyrenoids are sub-cellular micro-compartments found in chloroplasts of many algae, and in a single group of land plants, the hornworts. Pyrenoids are associated with the operation of a carbon-concentrating mechanism (CCM). Their main function is to act as centres of carbon dioxide (CO2) fixation, by generating and maintaining a CO2 rich environment around the photosynthetic enzyme ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO). Pyrenoids therefore seem to have a role analogous to that of carboxysomes in cyanobacteria.

Chlorophyll <i>b</i> Chemical compound

Chlorophyll b is a form of chlorophyll. Chlorophyll b helps in photosynthesis by absorbing light energy. It is more soluble than chlorophyll a in polar solvents because of its carbonyl group. Its color is green, and it primarily absorbs blue light.

<span class="mw-page-title-main">Etioplast</span>

Etioplasts are an intermediate type of plastid that develop from proplastids that have not been exposed to light, and convert into chloroplasts upon exposure to light. They are usually found in stem and leaf tissue of flowering plants (Angiosperms) grown either in complete darkness, or in extremely low-light conditions.

<span class="mw-page-title-main">Chlorophyllase</span>

Chlorophyllase is an essential enzyme in chlorophyll metabolism. It is a membrane proteins commonly known as chlase (EC 3.1.1.14, CLH) with systematic name chlorophyll chlorophyllidohydrolase. It catalyzes the reaction

<span class="mw-page-title-main">Divinyl chlorophyllide a 8-vinyl-reductase</span> Class of enzymes

In enzymology, divinyl chlorophyllide a 8-vinyl-reductase (EC 1.3.1.75) is an enzyme that catalyzes the chemical reaction

<span class="mw-page-title-main">Protochlorophyllide reductase</span>

In enzymology, protochlorophyllide reductases (POR) are enzymes that catalyze the conversion from protochlorophyllide to chlorophyllide a. They are oxidoreductases participating in the biosynthetic pathway to chlorophylls.

<span class="mw-page-title-main">Aldehyde dehydrogenase 18 family, member A1</span> Protein-coding gene in the species Homo sapiens

Delta-1-pyrroline-5-carboxylate synthetase (P5CS) is an enzyme that in humans is encoded by the ALDH18A1 gene. This gene is a member of the aldehyde dehydrogenase family and encodes a bifunctional ATP- and NADPH-dependent mitochondrial enzyme with both gamma-glutamyl kinase and gamma-glutamyl phosphate reductase activities. The encoded protein catalyzes the reduction of glutamate to delta1-pyrroline-5-carboxylate, a critical step in the de novo biosynthesis of proline, ornithine and arginine. Mutations in this gene lead to hyperammonemia, hypoornithinemia, hypocitrullinemia, hypoargininemia and hypoprolinemia and may be associated with neurodegeneration, cataracts and connective tissue diseases. Alternatively spliced transcript variants, encoding different isoforms, have been described for this gene. As reported by Bruno Reversade and colleagues, ALDH18A1 deficiency or dominant-negative mutations in P5CS in humans causes a progeroid disease known as De Barsy Syndrome.

<span class="mw-page-title-main">Phototropism</span> Growth of a plant in response to a light stimulus

In biology, phototropism is the growth of an organism in response to a light stimulus. Phototropism is most often observed in plants, but can also occur in other organisms such as fungi. The cells on the plant that are farthest from the light contain a hormone called auxin that reacts when phototropism occurs. This causes the plant to have elongated cells on the furthest side from the light. Phototropism is one of the many plant tropisms, or movements, which respond to external stimuli. Growth towards a light source is called positive phototropism, while growth away from light is called negative phototropism. Negative phototropism is not to be confused with skototropism, which is defined as the growth towards darkness, whereas negative phototropism can refer to either the growth away from a light source or towards the darkness. Most plant shoots exhibit positive phototropism, and rearrange their chloroplasts in the leaves to maximize photosynthetic energy and promote growth. Some vine shoot tips exhibit negative phototropism, which allows them to grow towards dark, solid objects and climb them. The combination of phototropism and gravitropism allow plants to grow in the correct direction.

Plastoglobulins is a family of proteins prominent found in lipid globules in plastids of flowering plants. It shows sequence similarities to the PAP/fibrillin family. PGL and similar proteins can be found in most algae, cyanobacteria and plants, but no other life forms; it suggests a role for PGL in oxygenic photosynthesis.

<span class="mw-page-title-main">Chlorophyllide-a oxygenase</span> Class of enzymes

Chlorophyllide-a oxygenase (EC 1.14.13.122), chlorophyllide a oxygenase, chlorophyll-b synthase, CAO) is an enzyme with systematic name chlorophyllide-a:oxygen 7-oxidoreductase. This enzyme catalyses the following chemical reactions

<span class="mw-page-title-main">Magnesium-protoporphyrin IX monomethyl ester (oxidative) cyclase</span> Class of enzymes

Magnesium-protoporphyrin IX monomethyl ester (oxidative) cyclase, is an enzyme with systematic name magnesium-protoporphyrin-IX 13-monomethyl ester, ferredoxin:oxygen oxidoreductase (hydroxylating). In plants this enzyme catalyses the following overall chemical reaction

Plastid terminal oxidase or plastoquinol terminal oxidase (PTOX) is an enzyme that resides on the thylakoid membranes of plant and algae chloroplasts and on the membranes of cyanobacteria. The enzyme was hypothesized to exist as a photosynthetic oxidase in 1982 and was verified by sequence similarity to the mitochondrial alternative oxidase (AOX). The two oxidases evolved from a common ancestral protein in prokaryotes, and they are so functionally and structurally similar that a thylakoid-localized AOX can restore the function of a PTOX knockout.

Circadian Clock Associated 1 (CCA1) is a gene that is central to the circadian oscillator of angiosperms. It was first identified in Arabidopsis thaliana in 1993. CCA1 interacts with LHY and TOC1 to form the core of the oscillator system. CCA1 expression peaks at dawn. Loss of CCA1 function leads to a shortened period in the expression of many other genes.

<span class="mw-page-title-main">Chlorophyllide</span> Chemical compound

Chlorophyllide a and Chlorophyllide b are the biosynthetic precursors of chlorophyll a and chlorophyll b respectively. Their propionic acid groups are converted to phytyl esters by the enzyme chlorophyll synthase in the final step of the pathway. Thus the main interest in these chemical compounds has been in the study of chlorophyll biosynthesis in plants, algae and cyanobacteria. Chlorophyllide a is also an intermediate in the biosynthesis of bacteriochlorophylls.

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.

References

  1. KEGG compound database entry
  2. Willows, Robert D. (2003). "Biosynthesis of chlorophylls from protoporphyrin IX". Natural Product Reports. 20 (6): 327–341. doi:10.1039/B110549N. PMID   12828371.
  3. 1 2 Meskauskiene R, Nater M, Goslings D, Kessler F, op den Camp R, Apel K. FLU: a negative regulator of chlorophyll biosynthesis in Arabidopsis thaliana. Proceedings of the National Academy of Sciences of the United States of America. 2001; 98(22):12826-31 pdf.
  4. R. Caspi (2007-07-18). "3,8-divinyl-chlorophyllide a biosynthesis I (aerobic, light-dependent)". MetaCyc Metabolic Pathway Database. Retrieved 2020-06-04.
  5. KEGG enzyme entry 1.3.1.33
  6. Yuichi FujitaDagger and Carl E. Bauer (2000). Reconstitution of Light-independent Protochlorophyllide Reductase from Purified Bchl and BchN-BchB Subunits. J. Biol. Chem., Vol. 275, Issue 31, 23583-23588.
  7. S.Yamazaki, J.Nomata, Y.Fujita (2006) Differential operation of dual protochlorophyllide reductases for chlorophyll biosynthesis in response to environmental oxygen levels in the cyanobacterium Leptolyngbya boryana. Plant Physiology, 2006, 142, 911-922
  8. J Li, M Goldschmidt-Clermont, M P Timko (1997). Chloroplast-encoded chlB is required for light-independent protochlorophyllide reductase activity in Chlamydomonas reinhardtii. Plant Cell 5(12): 1817–1829. .
  9. 1 2 Lee, Keun Pyo; Kim, Chanhong; Lee, Dae Won; Apel, Klaus (2003). "TIGRINA d, required for regulating the biosynthesis of tetrapyrroles in barley, is an ortholog of the FLU gene of Arabidopsis thaliana". FEBS Letters. 553 (1–2): 119–124. doi:10.1016/s0014-5793(03)00983-9. PMID   14550558. S2CID   34038176.
  10. A Falciatore, L Merendino, F Barneche, M Ceol, R Meskauskiene, K Apel, JD Rochaix (2005). The FLP proteins act as regulators of chlorophyll synthesis in response to light and plastid signals in Chlamydomonas. Genes & Dev, 19:176-187