author_facet Webster, D
Jondorf, W. R
Dixon, H B. F.
Webster, D
Jondorf, W. R
Dixon, H B. F.
author Webster, D
Jondorf, W. R
Dixon, H B. F.
spellingShingle Webster, D
Jondorf, W. R
Dixon, H B. F.
Biochemical Journal
Phosphonomethyl analogues of hexose phosphates
Cell Biology
Molecular Biology
Biochemistry
author_sort webster, d
spelling Webster, D Jondorf, W. R Dixon, H B. F. 0264-6021 Portland Press Ltd. Cell Biology Molecular Biology Biochemistry http://dx.doi.org/10.1042/bj1550433 <jats:p>The analogue of fructose 1,6-bisphosphate in which the phosphate group, -O-PO3H2, on C-6 is replaced by the phosphonomethyl group, -CH2-PO3H2, was made enzymically from the corresponding analogue of 3-phosphoglycerate. It was a substrate for aldolase, which was used to form it, but not for fructose 1,6-bisphosphatase. It was hydrolysed chemically to yield the corresponding analogue of fructose 6-phosphate [i.e. 6-deoxy-6-(phosphonomethyl)-D-fructose, or, more strictly, 6,7-dideoxy-7-phosphono-D-arabino-2-heptulose]. This proved to be a substrate for the sequential actions of glucose 6-phosphate isomerase, glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase. Thus seven out of the nine enzymes of the glycolytic and pentose phosphate pathways so far tested catalyse the reactions of the phosphonomethyl isosteres of their substrates.</jats:p> Phosphonomethyl analogues of hexose phosphates Biochemical Journal
doi_str_mv 10.1042/bj1550433
facet_avail Online
Free
finc_class_facet Biologie
Chemie und Pharmazie
format ElectronicArticle
fullrecord blob:ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTA0Mi9iajE1NTA0MzM
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTA0Mi9iajE1NTA0MzM
institution DE-Bn3
DE-Brt1
DE-Zwi2
DE-D161
DE-Gla1
DE-Zi4
DE-15
DE-Pl11
DE-Rs1
DE-105
DE-14
DE-Ch1
DE-L229
DE-D275
imprint Portland Press Ltd., 1976
imprint_str_mv Portland Press Ltd., 1976
issn 0264-6021
issn_str_mv 0264-6021
language English
mega_collection Portland Press Ltd. (CrossRef)
match_str webster1976phosphonomethylanaloguesofhexosephosphates
publishDateSort 1976
publisher Portland Press Ltd.
recordtype ai
record_format ai
series Biochemical Journal
source_id 49
title Phosphonomethyl analogues of hexose phosphates
title_unstemmed Phosphonomethyl analogues of hexose phosphates
title_full Phosphonomethyl analogues of hexose phosphates
title_fullStr Phosphonomethyl analogues of hexose phosphates
title_full_unstemmed Phosphonomethyl analogues of hexose phosphates
title_short Phosphonomethyl analogues of hexose phosphates
title_sort phosphonomethyl analogues of hexose phosphates
topic Cell Biology
Molecular Biology
Biochemistry
url http://dx.doi.org/10.1042/bj1550433
publishDate 1976
physical 433-441
description <jats:p>The analogue of fructose 1,6-bisphosphate in which the phosphate group, -O-PO3H2, on C-6 is replaced by the phosphonomethyl group, -CH2-PO3H2, was made enzymically from the corresponding analogue of 3-phosphoglycerate. It was a substrate for aldolase, which was used to form it, but not for fructose 1,6-bisphosphatase. It was hydrolysed chemically to yield the corresponding analogue of fructose 6-phosphate [i.e. 6-deoxy-6-(phosphonomethyl)-D-fructose, or, more strictly, 6,7-dideoxy-7-phosphono-D-arabino-2-heptulose]. This proved to be a substrate for the sequential actions of glucose 6-phosphate isomerase, glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase. Thus seven out of the nine enzymes of the glycolytic and pentose phosphate pathways so far tested catalyse the reactions of the phosphonomethyl isosteres of their substrates.</jats:p>
container_issue 2
container_start_page 433
container_title Biochemical Journal
container_volume 155
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
_version_ 1792332777859842061
geogr_code not assigned
last_indexed 2024-03-01T14:02:14.315Z
geogr_code_person not assigned
openURL url_ver=Z39.88-2004&ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fvufind.svn.sourceforge.net%3Agenerator&rft.title=Phosphonomethyl+analogues+of+hexose+phosphates&rft.date=1976-05-01&genre=article&issn=0264-6021&volume=155&issue=2&spage=433&epage=441&pages=433-441&jtitle=Biochemical+Journal&atitle=Phosphonomethyl+analogues+of+hexose+phosphates&aulast=Dixon&aufirst=H+B.+F.&rft_id=info%3Adoi%2F10.1042%2Fbj1550433&rft.language%5B0%5D=eng
SOLR
_version_ 1792332777859842061
author Webster, D, Jondorf, W. R, Dixon, H B. F.
author_facet Webster, D, Jondorf, W. R, Dixon, H B. F., Webster, D, Jondorf, W. R, Dixon, H B. F.
author_sort webster, d
container_issue 2
container_start_page 433
container_title Biochemical Journal
container_volume 155
description <jats:p>The analogue of fructose 1,6-bisphosphate in which the phosphate group, -O-PO3H2, on C-6 is replaced by the phosphonomethyl group, -CH2-PO3H2, was made enzymically from the corresponding analogue of 3-phosphoglycerate. It was a substrate for aldolase, which was used to form it, but not for fructose 1,6-bisphosphatase. It was hydrolysed chemically to yield the corresponding analogue of fructose 6-phosphate [i.e. 6-deoxy-6-(phosphonomethyl)-D-fructose, or, more strictly, 6,7-dideoxy-7-phosphono-D-arabino-2-heptulose]. This proved to be a substrate for the sequential actions of glucose 6-phosphate isomerase, glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase. Thus seven out of the nine enzymes of the glycolytic and pentose phosphate pathways so far tested catalyse the reactions of the phosphonomethyl isosteres of their substrates.</jats:p>
doi_str_mv 10.1042/bj1550433
facet_avail Online, Free
finc_class_facet Biologie, Chemie und Pharmazie
format ElectronicArticle
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
geogr_code not assigned
geogr_code_person not assigned
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTA0Mi9iajE1NTA0MzM
imprint Portland Press Ltd., 1976
imprint_str_mv Portland Press Ltd., 1976
institution DE-Bn3, DE-Brt1, DE-Zwi2, DE-D161, DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229, DE-D275
issn 0264-6021
issn_str_mv 0264-6021
language English
last_indexed 2024-03-01T14:02:14.315Z
match_str webster1976phosphonomethylanaloguesofhexosephosphates
mega_collection Portland Press Ltd. (CrossRef)
physical 433-441
publishDate 1976
publishDateSort 1976
publisher Portland Press Ltd.
record_format ai
recordtype ai
series Biochemical Journal
source_id 49
spelling Webster, D Jondorf, W. R Dixon, H B. F. 0264-6021 Portland Press Ltd. Cell Biology Molecular Biology Biochemistry http://dx.doi.org/10.1042/bj1550433 <jats:p>The analogue of fructose 1,6-bisphosphate in which the phosphate group, -O-PO3H2, on C-6 is replaced by the phosphonomethyl group, -CH2-PO3H2, was made enzymically from the corresponding analogue of 3-phosphoglycerate. It was a substrate for aldolase, which was used to form it, but not for fructose 1,6-bisphosphatase. It was hydrolysed chemically to yield the corresponding analogue of fructose 6-phosphate [i.e. 6-deoxy-6-(phosphonomethyl)-D-fructose, or, more strictly, 6,7-dideoxy-7-phosphono-D-arabino-2-heptulose]. This proved to be a substrate for the sequential actions of glucose 6-phosphate isomerase, glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase. Thus seven out of the nine enzymes of the glycolytic and pentose phosphate pathways so far tested catalyse the reactions of the phosphonomethyl isosteres of their substrates.</jats:p> Phosphonomethyl analogues of hexose phosphates Biochemical Journal
spellingShingle Webster, D, Jondorf, W. R, Dixon, H B. F., Biochemical Journal, Phosphonomethyl analogues of hexose phosphates, Cell Biology, Molecular Biology, Biochemistry
title Phosphonomethyl analogues of hexose phosphates
title_full Phosphonomethyl analogues of hexose phosphates
title_fullStr Phosphonomethyl analogues of hexose phosphates
title_full_unstemmed Phosphonomethyl analogues of hexose phosphates
title_short Phosphonomethyl analogues of hexose phosphates
title_sort phosphonomethyl analogues of hexose phosphates
title_unstemmed Phosphonomethyl analogues of hexose phosphates
topic Cell Biology, Molecular Biology, Biochemistry
url http://dx.doi.org/10.1042/bj1550433