Protein Variants | Comment | Organism |
---|---|---|
additional information | in the homologous system with both components from barley leaves, the slightly more polar pFCC-1 is produced, whereas the combination of barley membranes with soluble protein from spinach yields the less polar pFCC-2 | Spinacia oleracea |
additional information | in the homologous system with both components from barley leaves, the slightly more polar pFCC-1 is produced, whereas the combination of barley membranes with soluble protein from spinach yields the less polar pFCC-2 | Hordeum vulgare |
Inhibitors | Comment | Organism | Structure |
---|---|---|---|
additional information | inactivation of RCCR by secondary compounds during tissue homogenization | Euptelea | |
additional information | inactivation of RCCR by secondary compounds during tissue homogenization | Ginkgo biloba | |
additional information | inactivation of RCCR by secondary compounds during tissue homogenization | Metasequoia |
Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|
chloroplast | - |
Auxenochlorella protothecoides | 9507 | - |
gerontoplast | - |
Spinacia oleracea | 34400 | - |
gerontoplast | - |
Selaginella sp. | 34400 | - |
gerontoplast | - |
Tropaeolum majus | 34400 | - |
gerontoplast | - |
Ginkgo biloba | 34400 | - |
gerontoplast | - |
Taxus baccata | 34400 | - |
gerontoplast | - |
Equisetum sp. | 34400 | - |
gerontoplast | - |
Cycas sp. | 34400 | - |
gerontoplast | - |
Cleome graveolens | 34400 | - |
gerontoplast | - |
Hordeum vulgare | 34400 | - |
gerontoplast | - |
Psilotum | 34400 | - |
gerontoplast | - |
Angiopteris | 34400 | - |
gerontoplast | - |
Metasequoia | 34400 | - |
gerontoplast | - |
Euptelea | 34400 | - |
gerontoplast | - |
Picea | 34400 | - |
gerontoplast | membrane | Solanum lycopersicum | 34400 | - |
gerontoplast | membrane | Selaginella sp. | 34400 | - |
gerontoplast | membrane | Tropaeolum majus | 34400 | - |
gerontoplast | membrane | Taxus sp. | 34400 | - |
gerontoplast | membrane | Carex | 34400 | - |
gerontoplast | membrane | Equisetum sp. | 34400 | - |
gerontoplast | membrane | Cleome graveolens | 34400 | - |
membrane | - |
Solanum lycopersicum | 16020 | - |
membrane | - |
Selaginella sp. | 16020 | - |
membrane | - |
Tropaeolum majus | 16020 | - |
membrane | - |
Taxus sp. | 16020 | - |
membrane | - |
Carex | 16020 | - |
membrane | - |
Equisetum sp. | 16020 | - |
membrane | - |
Cycas sp. | 16020 | - |
membrane | - |
Cleome graveolens | 16020 | - |
soluble | - |
Hordeum vulgare | - |
- |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Spinacia oleracea | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Selaginella sp. | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Tropaeolum majus | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Auxenochlorella protothecoides | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Ginkgo biloba | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Taxus baccata | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Equisetum sp. | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Cycas sp. | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Cleome graveolens | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Hordeum vulgare | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Psilotum | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Angiopteris | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Metasequoia | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Euptelea | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | Picea | - |
primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Angiopteris | - |
- |
- |
Auxenochlorella protothecoides | - |
- |
- |
Carex | - |
- |
- |
Cleome graveolens | - |
- |
- |
Cycas sp. | - |
- |
- |
Equisetum sp. | - |
- |
- |
Euptelea | - |
- |
- |
Ginkgo biloba | - |
- |
- |
Hordeum vulgare | Q9MTQ6 | - |
- |
Metasequoia | - |
- |
- |
Picea | - |
- |
- |
Psilotum | - |
- |
- |
Selaginella sp. | - |
- |
- |
Solanum lycopersicum | - |
- |
- |
Spinacia oleracea | - |
- |
- |
Taxus baccata | - |
- |
- |
Taxus sp. | - |
- |
- |
Tropaeolum majus | - |
- |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
cell culture | - |
Auxenochlorella protothecoides | - |
leaf | the enzyme is not only present in senescent leaves but also at other stages of leaf development | Solanum lycopersicum | - |
leaf | the enzyme is not only present in senescent leaves but also at other stages of leaf development | Selaginella sp. | - |
leaf | the enzyme is not only present in senescent leaves but also at other stages of leaf development | Tropaeolum majus | - |
leaf | the enzyme is not only present in senescent leaves but also at other stages of leaf development | Taxus sp. | - |
leaf | the enzyme is not only present in senescent leaves but also at other stages of leaf development | Carex | - |
leaf | the enzyme is not only present in senescent leaves but also at other stages of leaf development | Equisetum sp. | - |
leaf | the enzyme is not only present in senescent leaves but also at other stages of leaf development | Cycas sp. | - |
leaf | the enzyme is not only present in senescent leaves but also at other stages of leaf development | Cleome graveolens | - |
leaf | enzyme RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Selaginella sp. | - |
leaf | enzyme RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Tropaeolum majus | - |
leaf | enzyme RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Ginkgo biloba | - |
leaf | enzyme RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Taxus baccata | - |
leaf | enzyme RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Equisetum sp. | - |
leaf | enzyme RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Cycas sp. | - |
leaf | enzyme RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Cleome graveolens | - |
leaf | enzyme RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Psilotum | - |
leaf | enzyme RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Angiopteris | - |
leaf | enzyme RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Metasequoia | - |
leaf | enzyme RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Euptelea | - |
leaf | enzyme RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Picea | - |
leaf | primary leaves of barley which had been induced to senesce in permanent darkness for 3 days. RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Spinacia oleracea | - |
leaf | primary leaves of barley which had been induced to senesce in permanent darkness for 3 days. RCCR is a constitutive enzyme which is not only present in senescent leaves but also at other stages of leaf development | Hordeum vulgare | - |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Spinacia oleracea | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Selaginella sp. | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Tropaeolum majus | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Auxenochlorella protothecoides | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Ginkgo biloba | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Taxus baccata | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Equisetum sp. | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Cycas sp. | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Cleome graveolens | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Hordeum vulgare | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Psilotum | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Angiopteris | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Metasequoia | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Euptelea | ? | - |
? | |
additional information | when heterologous combinations of PaO and RCCR are tested, the type of primary fluorescent chlorophyll catabolite turns out to be invariably determined by the source of RCCR, i.e. the slightly more polar pFCC-1 or the less polar pFCC-2 | Picea | ? | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Spinacia oleracea | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Selaginella sp. | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Tropaeolum majus | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Auxenochlorella protothecoides | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Ginkgo biloba | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Taxus baccata | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Equisetum sp. | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Cycas sp. | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Cleome graveolens | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Hordeum vulgare | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Psilotum | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Angiopteris | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Metasequoia | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Euptelea | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Picea | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | - |
? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Tropaeolum majus | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | catabolite pFCC-0, possible representing a modified version of either pFCC-1 or -2 | ? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Cleome graveolens | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | catabolite pFCC-0, possible representing a modified version of either pFCC-1 or -2 | ? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Selaginella sp. | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | catabolite pFCC-3 | ? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Taxus baccata | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | catabolite pFCC-3 | ? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Equisetum sp. | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | catabolite pFCC-3 | ? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Cycas sp. | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | catabolite pFCC-3 | ? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Psilotum | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | catabolite pFCC-3 | ? | |
red chlorophyll catabolite + 2 reduced ferredoxin [iron-sulfur] cluster + 2 H+ | - |
Angiopteris | primary fluorescent chlorophyll catabolite + 2 oxidized ferredoxin [iron-sulfur] cluster | catabolite pFCC-3 | ? |
Synonyms | Comment | Organism |
---|---|---|
RCC reductase | - |
Spinacia oleracea |
RCC reductase | - |
Selaginella sp. |
RCC reductase | - |
Tropaeolum majus |
RCC reductase | - |
Auxenochlorella protothecoides |
RCC reductase | - |
Ginkgo biloba |
RCC reductase | - |
Taxus baccata |
RCC reductase | - |
Equisetum sp. |
RCC reductase | - |
Cycas sp. |
RCC reductase | - |
Cleome graveolens |
RCC reductase | - |
Hordeum vulgare |
RCC reductase | - |
Psilotum |
RCC reductase | - |
Angiopteris |
RCC reductase | - |
Metasequoia |
RCC reductase | - |
Euptelea |
RCC reductase | - |
Picea |
RCCR-1 | - |
Hordeum vulgare |
RCCR-2 | - |
Picea |
Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|
22 | - |
assay at room temperature | Hordeum vulgare |
pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|
8 | - |
assay at | Hordeum vulgare |
Cofactor | Comment | Organism | Structure |
---|---|---|---|
Ferredoxin | - |
Spinacia oleracea | |
Ferredoxin | - |
Selaginella sp. | |
Ferredoxin | - |
Tropaeolum majus | |
Ferredoxin | - |
Auxenochlorella protothecoides | |
Ferredoxin | - |
Ginkgo biloba | |
Ferredoxin | - |
Taxus baccata | |
Ferredoxin | - |
Equisetum sp. | |
Ferredoxin | - |
Cycas sp. | |
Ferredoxin | - |
Cleome graveolens | |
Ferredoxin | - |
Hordeum vulgare | |
Ferredoxin | - |
Psilotum | |
Ferredoxin | - |
Angiopteris | |
Ferredoxin | - |
Metasequoia | |
Ferredoxin | - |
Euptelea | |
Ferredoxin | - |
Picea |
General Information | Comment | Organism |
---|---|---|
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCC-2. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Spinacia oleracea |
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCC-2. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Selaginella sp. |
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCC-2. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Tropaeolum majus |
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCC-2. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Taxus baccata |
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCC-2. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Equisetum sp. |
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCC-2. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Cycas sp. |
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCC-2. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Cleome graveolens |
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCC-2. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Hordeum vulgare |
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCC-2. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Psilotum |
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCC-2. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Angiopteris |
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Ginkgo biloba |
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Metasequoia |
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Euptelea |
evolution | evolutionary tree of vascular plants based on analysis of several molecular data sets for enzymes RCCR, overview. Two forms of primary fluorescent chlorophyll catabolite, pFCC, are found in plants, the slightly more polar pFCC-1 or the less polar pFCC-2. A third form, pFCC-3 is found only in basal pteridophytes and in some gymnosperms, it seems to be produced by an ancestral type of RCCR. RCCR-1 appears to have evolved independently in some unrelated lineages. It has a restricted phylogenetic distribution and most likely represents recent derivations from RCCR-2. The situation within monocots appears to be quite clear cut. All the grasses and Carex tested are characterized by type 1 of RCCR, all other monocots produce pFCC-2 | Picea |
evolution | in chlorophyll breakdown, the basic mechanism of macrocycle cleavage appears to be the same in green algae and in angiosperms | Auxenochlorella protothecoides |