ライフサイエンスコーパス: phosphinothricin

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1 r we report that pita has no activity toward phosphinothricin.

2 binding pocket is complementary to those of phosphinothricin.

3 erminated on the MS medium supplemented with phosphinothricin (5 mg/l), confirming that the male ster

4 Specifically, we test whether phosphinothricin acetyl transferase (PAT) that confers h

5 Bialaphos resistance (BAR) and phosphinothricin acetyltransferase (PAT) genes, which co

6 ajority of these have been assigned putative phosphinothricin acetyltransferase activity, their true

7 clear expression of a bar transgene encoding phosphinothricin acetyltransferase, a detoxifying enzyme

8 y resistance to the broad-spectrum herbicide phosphinothricin (also known as glufosinate) via N-acety

9 y was inhibited by serine, alanine, glycine, phosphinothricin, and methionine sulfoximine.

10 One oxygen of the phosphinyl group of phosphinothricin appears to be protonated, because of it

11 tripeptide, contains the unusual amino acid phosphinothricin attached to two alanine residues.

12 model is used to determine the structure of phosphinothricin complexed to GS by difference Fourier m

13 Synthetic phosphinothricin (glufosinate) is a component of two top

14 er free Nt-pCK2-Int plants were resistant to phosphinothricin herbicides since the pCK2 plastid vecto

15 y, the plastid-lethal markers, glyphosate or phosphinothricin herbicides, were used to develop a sele

16 Phosphinothricin is a potent inhibitor of the enzyme glu

17 Phosphinothricin occupies the glutamate substrate pocket

18 and PAT exhibit substrate preference toward phosphinothricin over the 20 proteinogenic amino acids (

19 Phosphinothricin (PPT) is the active component of a fami

20 d as opposed to only 0.41% recovery when bar/phosphinothricin (PPT) selection was used.

21 biotic fosfomycin, the widely used herbicide phosphinothricin (PT), and the clinical candidate for tr

22 The late stages of biosynthesis of phosphinothricin tripeptide (PTT) involve peptide format

23 c and biochemical studies showed that during phosphinothricin tripeptide biosynthesis 2-hydroxyethylp

24 biosynthesis of the antibiotics fosfomycin, phosphinothricin tripeptide, and dehydrophos (formerly A

25 One such compound, phosphinothricin tripeptide, contains the unusual amino

26 ynthetic pathway to the commercial herbicide phosphinothricin, uncovered an example of such an O-H-bo

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