1 ed by replacement of external Cl- by SCN- or isethionate.

2 ctedly, by reduction of sulfoacetaldehyde to isethionate (2-hydroxyethanesulfonate) by an NADH-depend

3 ng this enzyme negatively affects the use of isethionate and taurine as sulfur sources by S. cerevisi

4 ized, with the best natural substrates being isethionate and taurocholate.

5 tants of D. alaskensis G20 did not grow with isethionate as the terminal electron acceptor.

6  and Desulfovibrio alaskensis G20, which use isethionate but not taurine; corresponding knockout muta

7    After replacing external NaCl with sodium isethionate, E(rev) for the second component shifted to

8 erapy (nystatin eye ointment and propamidine isethionate eye drops) was administered, resulting in si

9                                              Isethionate is then cleaved to sulfite and acetaldehyde

10 roximately proprionate (Prop-) approximately isethionate (Ise-) approximately F- approximately PO4-.

11 -) is a sacrificial anion such as glycolate, isethionate, or nitrate.

12 ble B. wadsworthia to metabolise taurine and isethionate, producing H(2)S, acetate, and ethanol.

13 h-clamp studies employing symmetrical sodium isethionate solutions.

14 uncharacterized glycyl radical enzyme (GRE), isethionate sulfite-lyase (IslA).

15 es the radical-mediated C-S bond cleavage of isethionate to form sulfite and acetaldehyde.

16 evelopment of a new oral form of pentamidine isethionate VLX103, led to investigations of the effecti

17     Of the various drugs tested, pentamidine isethionate was most effective against amebas (ca. 90% i