Elm1p, Pak1p, and Tos3p are upstream kinases for the SNF1 complex that have partially redundant functions.

Sphingosine kinases catalyze the formation of sphingosine 1-phosphate, a bioactive lipid involved in many aspects of cellular regulation, including the fundamental biological processes of cell growth and survival. A diverse range of cell agonists induce activation of human sphingosine kinase 1 (hSK1) and, commonly, its translocation to the plasma membrane. Although the activation of hSK1 in response to at least some agonists occurs directly via its phosphorylation at Ser 225 by ERK1/2, many aspects governing the regulation of this phosphorylation and subsequent translocation remain unknown. Here, in an attempt to understand some of these processes, we have examined the known interaction of hSK1 with calmodulin (CaM). By using a combination of limited proteolysis, peptide interaction analysis, and site-directed mutagenesis, we have identified that the CaM-binding site of hSK1 resides in the region spanned by residues 191-206. Specifically, Phe 197 and Leu 198 are critically involved in the interaction because a version of hSK1 incorporating mutations of both Phe 197 3 Ala and Leu 198 3 Gln failed to bind CaM. We have also shown for the first time that human sphingosine kinase 2 (hSK2) binds CaM, and does so via a CaM binding region that is conserved with hSK1 because comparable mutations in hSK2 also ablate CaM binding to this protein. By using the CaM-binding-deficient version of hSK1, we have begun to elucidate the role of CaM in hSK1 regulation by demonstrating that disruption of the CaM-binding site ablates agonist-induced translocation of hSK1 from the cytoplasm to the plasma membrane, while having no effect on hSK1 phosphorylation and catalytic activation.Sphingosine kinases are important signaling enzymes because of their role in the synthesis of the bioactive lipid sphingosine 1-phosphate (S1P).3 Many studies have shown that S1P can affect a diverse array of biological processes, including calcium mobilization, mitogenesis, apoptosis, atherosclerosis, inflammatory responses, cell motility, and angiogenesis (1-4). Although some of these varied effects of S1P result from its action as a ligand for S1P-specific cell-surface G-protein-coupled receptors (5), significant evidence now exists that indicates S1P can also function intracellularly as a second messenger, particularly in the regulation of cell proliferation and apoptosis (6).Two sphingosine kinases exist in humans (hSK1 and hSK2), with most studies to date focusing on hSK1. Although these two enzymes originate from different genes and differ in size, tissue distribution, developmental expression, substrate specificity, specific activity, and possibly in their cellular roles (7-10), their polypeptide sequences possess a high degree of similarity. In fact, almost all of the hSK1 sequence aligns with regions of the larger hSK2 sequence with 80% overall similarity (45% identity) (7). However, hSK2 also possesses two additional polypeptide regions at its N terminus and within the central region of its sequence that are quite distinct from hSK1.Although hSK...

Wine yeast, in common with other industrial Saccharomyces cerevisiae yeast, can produce hydrogen sulfide during alcoholic fermentation. The aim of this work was to evaluate a genetic strategy for reducing hydrogen sulfide production by lowering the activity of NADPH-dependent sulfite reductase, a key enzyme in the biosynthesis of the sulfur-containing amino acids. The role of amino acids predicted to be necessary for cofactor binding was investigated by comparisons with other proteins in the ferredoxin family. Substitutions in the glycine-rich loop domain (glycines 891 and 893) and at serine 953 of the alpha subunit, Met10p, appear to strongly affect NADPH binding. However, mutations in two amino acids that are completely conserved within the NADPH binding domain of the ferredoxin reductase family, lysine 959 and cysteine 987, have minimal effect on enzyme activity. Serine 820 is indicated to be essential for efficient FAD binding. The two-hybrid system was used to confirm that Met10p interacts with Met5p, the predicted beta subunit of sulfite reductase. Binding of the subunits could only be demonstrated in the absence of methionine, indicating that an additional factor, possibly siroheme, is required to mediate this interaction. Strategies to decrease, but not eliminate, sulfite reductase activity in the cell using identified mutants were tested, and the findings are discussed with the a view to producing improved wine strains.