Any feedback?
Please rate this page
(search_result.php)
(0/150)

BRENDA support

Refine search

Search Substrates and Products (Substrate)

show results
Don't show organism specific information (fast!)
Search organism in taxonomic tree (slow, choose "exact" as search mode, e.g. "mammalia" for rat,human,monkey,...)
(Not possible to combine with the first option)
Refine your search

Search term:

Results 1 - 10 of 69 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.1402 sucrose - Leuconostoc citreum ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.140more LC/MS product analysis Leuconostoc citreum ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.140more alternansucrase enzyme from Leuconostoc citreum SK24.002 is used to produce di-glycosyl-stevioside through acceptor reaction. Identification of the di-glycosyl-stevioside structure as 13-([alpha-D-glucopyranosyl-(1->3)-alpha-D-glucopyranosyl-(1->6)-beta-D glucopyranosyl-(1->2)-beta-D-glucopyranosyl]oxy)kaur-16-en-19-oic acid beta-D glucopyranosyl ester, method optimization and evaluation, overview Leuconostoc citreum ? - -
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.140more for the docking calculations, a model of the ASRDELTA2 glucosyl-enzyme intermediate is constructed based on the high resolution structure of the GH13 covalent intermediate (PDB ID 1S46). Maltose is the best known acceptor for ASR Leuconostoc citreum ? - -
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.140more product analysis, determination of alternan nanoparticle size distribution by dynamic light scattering Leuconostoc citreum ? - -
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.140stevioside + sucrose transglucosylation Leuconostoc citreum ? the product is composed of mono-, di-, and triglucosylated stevioside and their isomers ?
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.140sucrose + alpha-D-glucan - Leuconostoc citreum ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.140sucrose + maltose maltose undergoes alpha-1,6 glucosylation alone to give the oligodextran of DP3 (OD3 panose, alpha-D-Glcp-(1->6)-alpha-D-Glcp-(1->4)-D-Glc), which can be further elongated at either the O6 or the O3 position of the nonreducing unit to give the structures OD4 (alpha-D-Glcp-(1->6)-alpha-D-Glcp-(1->6)-alpha-D-Glcp-(1->4)-D-Glc) and OA4 (alpha-D-Glcp-(1->3)-alpha-D-Glcp-(1->6)-alpha-D-Glcp-(1->4)-D-Glc), respectively. The oligosaccharide OA4 is quick to appear at the beginning of the reaction (1 min) and accumulates at a much higher level than OD4, indicating that panose is preferentially elongated with an alpha-1,3 linkage. A very small peak of OD5 originating from OD4 only appears toward the end of the reaction (after about 30 min) and is not elongated further (no OD6 is found). As soon as the OA4 starts to accumulate, it is efficiently converts to OA5 (alpha-D-Glcp-(1->6)-alpha-D-Glcp-(1->3)-alpha-D-Glcp-(1->6)-alpha-D-Glcp-(1->4)-D-Glc). The OA5 itself can act as an acceptor for the formation of two OA6s (alpha-D-Glcp-(1->6)-alpha-D-Glcp-(1->6)-alpha-D-Glcp-(1->3)-alpha-D-Glcp-(1->6)-alpha-D-Glcp-(1->4)-DGlc and alpha-D-Glcp-(1->3)-alpha-D-Glcp-(1->6)-alpha-D-Glcp-(1->3)-alpha-D-Glcp-(1->6)-alpha-D-Glcp-(1->4)-D-Glc) Leuconostoc citreum ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.1402 sucrose - Leuconostoc citreum ABK-1 ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.140more product analysis, determination of alternan nanoparticle size distribution by dynamic light scattering Leuconostoc citreum ABK-1 ? - -
Results 1 - 10 of 69 > >>