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1 ucose serving as the terminal hydride donor (glucose dehydrogenase).
2 re-engineered component of glucometers: PQQ-glucose dehydrogenase.
3 ferentiated fiber cells also contain SDH and glucose dehydrogenase.
4 A (or ugd) that is predicted to encode a UDP-glucose dehydrogenase.
5 , that encodes a homologue of vertebrate UDP-glucose dehydrogenase.
6 ed with high similarity to the family of UDP-glucose dehydrogenases.
7 s flavus-derived flavin adenine dinucleotide glucose dehydrogenase (AfGDH) and an electron transfer d
8 a series of binary and ternary complexes of glucose dehydrogenase, an MDR enzyme from Haloferax medi
14 Using sensing electrode composed of wired glucose dehydrogenase and enzymatic reference electrode
16 second film (F2) contained also added enzyme glucose dehydrogenase and its cofactor beta-nicotinamide
17 ctate with using D-sorbitol dehydrogenase, D-glucose dehydrogenase and L-lactate dehydrogenase respec
18 that sqv-4 encodes a protein similar to UDP-glucose dehydrogenases and showed that the SQV-4 protein
19 arboxylethyl)-l-norvaline dehydrogenase, UDP-glucose dehydrogenase, and 6-phosphogluconate dehydrogen
20 minomethylpyridine)Cl].PF6, an FAD-dependent glucose dehydrogenase, and carbon nanotubes achieve curr
21 plexed electrodes with b2LOxS and a DET-type glucose dehydrogenase, and evaluated their performance i
22 sed of three enzymes (alcohol dehydrogenase, glucose dehydrogenase, and glucose oxidase) operating in
23 ity of these advances, alkaline phosphatase, glucose dehydrogenase, and laccase were screened for imm
26 lpha into pyrroloquinoline quinone-dependent glucose dehydrogenase by constructing and screening a co
28 engineering and application of FAD dependent glucose dehydrogenase complex (FADGDH) which is capable
29 which encodes a protein with homology to UDP-glucose dehydrogenase, compromise the synthesis of both
32 In this study, a novel fungus FAD dependent glucose dehydrogenase, derived from Aspergillus niger (A
33 he effect of possible contaminating enzymes (glucose dehydrogenase, EC 1.1.1.47; glucose 6-phosphatas
34 n aqueous solution, of the bacterial soluble glucose dehydrogenase enzyme.PQQ.glucose complex and int
37 Fungi-derived flavin adenine dinucleotide glucose dehydrogenases (FADGDHs) are currently the most
38 nascus thermophilus or soluble PQQ-dependent glucose dehydrogenase from Acinetobacter calcoaceticus.
39 the IPUT1 gene together with genes for a UDP-glucose dehydrogenase from Arabidopsis and a human UDP-G
40 elongata omega-transaminase (HeomegaT), and glucose dehydrogenase from Bacillus subtilis (BsGDH).
41 flavin adenine dinucleotide (FAD)-dependent glucose dehydrogenase from Glomerella cingulata (GcGDH)
42 s Blue-Reinecke salt, coated with the enzyme glucose dehydrogenase (from Bacillus sp.), and nicotinam
43 imary objectives were to: a) introduce a new glucose dehydrogenase (GD)-based electrochemical biosens
45 ors were developed using the model system of glucose dehydrogenase (GDH) and its nicotinamide adenine
47 a dealloyed nanoporous gold (NPG) supported glucose dehydrogenase (GDH) bioanode, immobilised with t
48 flavin adenine dinucleotide (FAD) dependent glucose dehydrogenase (GDH) complex, to elucidate its ch
49 lectrode based on the covalent attachment of glucose dehydrogenase (GDH) enzyme and safranin O to ami
50 es are being explored for efficiently wiring glucose dehydrogenase (GDh) enzymes capable of glucose (
51 s explored in order to covalently immobilize glucose dehydrogenase (GDH) in the CNT-CHIT films using
52 Flavin-adenine dinucleotide (FAD) dependent glucose dehydrogenase (GDH) is a thermostable, oxygen in
53 , which can be concurrently regenerated by a glucose dehydrogenase (GDH) using only 1.2 equiv of gluc
56 PQQ, the prosthetic group of the apo-enzyme glucose dehydrogenase (GDH), are used as the label to pr
57 (PQQ), the prosthetic group of the apoenzyme glucose dehydrogenase (GDH), are used to detect membrane
58 as a biocatalyst, NADPH as a cofactor, and a glucose dehydrogenase (GDH)-glucose cofactor regeneratio
62 nalyzed nucleotide sequence variation at the Glucose dehydrogenase (Gld) locus from four populations
63 (Adh), Alcohol dehydrogenase related (Adhr), Glucose dehydrogenase (Gld), and rosy (ry) genes (totali
64 ur immunity-related enzymes (phenol oxidase, glucose dehydrogenase, glucose oxidase, and lysozyme) we
65 substrate complex of a similar quinoprotein, glucose dehydrogenase, has recently been reported that s
68 e (PQQ) and the PQQ-dependent membrane-bound glucose dehydrogenase nearly eliminates bioleaching.
69 f cps2K, cps2J, or cps2H, which encode a UDP-glucose dehydrogenase necessary for side chain synthesis
71 systems of S. typhimurium; ugd, encoding UDP-glucose dehydrogenase; phoP, indicative that the phoPQ o
72 group 2 dehydrin proteins (pPCB2), a barely glucose dehydrogenase (pPCB6) and the glutathione S-tran
73 cally modified with pyrroloquinoline quinone glucose dehydrogenase (PQQ-GDH) and bilirubin oxidase (B
74 es with redox enzymes, pyroquinoline quinone glucose dehydrogenase (PQQ-GDH) and laccase functioning
75 ic current of pyrroloquinoline quinone (PQQ)-glucose dehydrogenase (PQQ-GDH) immobilized over electro
76 ogeneous reconstitution of the PQQ-dependent glucose dehydrogenase (PQQ-GDH) through the specific bin
78 hanism of electron transfer in PQQ-dependent glucose dehydrogenase (PQQ-sGDH) anodes has been determi
79 bling pyrroloquinoline quinone (PQQ)-soluble glucose dehydrogenase (PQQ-sGDH) from Acinetobacter calc
80 the anode pyrroloquinoline quinone dependent glucose dehydrogenase ((PQQ)GDH) has been immobilized on
81 ate arose predominantly by the action of UDP-glucose dehydrogenase rather than through the postulated
82 la Sugarless, a uridine 5'-diphosphate (UDP)-glucose dehydrogenase required for heparan sulfate, chon
83 arison of the GMD structure with that of UDP-glucose dehydrogenase reveals the structural basis of su
84 Mechanistically, this bacterium secretes glucose dehydrogenase (RyGDH), which acidifies the gut l
85 Asd and Acinetobacter calcoaceticus soluble glucose dehydrogenase (sGdh), with major structural diff
86 that Gcd1 encodes a novel NADP(+)-dependent glucose dehydrogenase that acts in a pathway with the Id
87 ort the crystal structure of the apo form of glucose dehydrogenase to a resolution of 1.8 A and a com
88 of substrates using a commercially available glucose dehydrogenase to drive its halogenase activity.
90 r dehydrogenase-based biosensing by allowing glucose dehydrogenase to spontaneously adsorb onto the N
92 induces transcription of the Salmonella UDP-glucose dehydrogenase ugd gene in an RcsA- and RcsB-depe
96 n zebrafish revealed a critical role for UDP-glucose dehydrogenase (UGDH) in valve development, so th
101 disrupts the single mouse gene encoding UDP-glucose dehydrogenase (Ugdh), an enzyme required for the
102 have generated a mesenchymal ablation of UDP-glucose dehydrogenase (Ugdh), an essential biosynthetic
103 aphite with glucose oxidase or FAD-dependent glucose dehydrogenase using a range of crosslinkers and
109 ter the NAD(+)/NADH ratio via the enzyme UDP-glucose dehydrogenase, which oxidizes the alcohol group
111 ation of glucose by Thermoplasma acidophilum glucose dehydrogenase with the concomitant oxidation of
112 EC was successfully prepared by constructing glucose dehydrogenase with two different catcher domains