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1 phospholipids, diacylglycerols, sterols, and sulfolipids.
2 e preparation of other analogues and natural sulfolipids.
3 ion in the expression of envelope-associated sulfolipids.
4 are minor constituents of acyltrehaloses and sulfolipids.
5   Consequently, pks2 mutant does not produce sulfolipids.
6 cids that are the major acyl constituents of sulfolipids.
7 ip similar to that between Chp1 and MmpL8 in sulfolipid 1 biosynthesis.
8 acterized as the terminal acyltransferase in sulfolipid 1 biosynthesis.
9 lar to that of another trehalose glycolipid, sulfolipid 1.
10 ons in vitro and identify the Mtb glycolipid sulfolipid-1 (SL-1) as the nociceptive molecule.
11                  One of the most abundant is sulfolipid-1 (SL-1), a tetraacyl-sulfotrehalose glycolip
12 ctors, phthiocerol dimycocerosate (PDIM) and sulfolipid-1 (SL-1), are controlled by the availability
13                         One such glycolipid, Sulfolipid-1 (SL-1), consists of a trehalose-2-sulfate (
14 ents, notably the cell wall-associated lipid sulfolipid-1 (SL-1), which functions through the mTOR co
15 able lipids is a sulfated glycolipid, termed sulfolipid-1 (SL-1), which is thought to mediate specifi
16 ic machinery has no cross-talk with that for sulfolipid-1 despite their related structures.
17 rehalose is required for the biosynthesis of sulfolipid-1, the most abundant sulfated metabolite foun
18  studied M. tuberculosis cell wall component sulfolipid-1.
19 relevant glycolipids such as cord factor and sulfolipid-1.
20  Here, we describe an acylated derivative of sulfolipid, 2'-O-acyl-sulfoquinovosyldiacylglycerol (ASQ
21  consistently with a phosphatidylglycerol-to-sulfolipid and a phosphatidycholine-to-betaine lipid rep
22 ltransferase Chp1 accepts a synthetic diacyl sulfolipid and transfers an acyl group regioselectively
23                             Tetra-O-acylated sulfolipids are metabolites found in the cell wall of My
24 ould have been recruited for sulfolactate or sulfolipid biosyntheses.
25  arises from the sugar nucleotide pathway of sulfolipid biosynthesis by acylation of the 2'-hydroxyl
26            A novel gene, sqdX, essential for sulfolipid biosynthesis in the cyanobacterium Synechococ
27 SQD2 in Escherichia coli reconstituted plant sulfolipid biosynthesis in this bacterium.
28                                              Sulfolipid biosynthesis involves the transfer of sulfoqu
29 syltransferase catalyzing the second step of sulfolipid biosynthesis.
30      The results support the hypothesis that sulfolipid can function as a substitute of anionic phosp
31 is of the sulfoquinovosyl headgroup of plant sulfolipids, catalyzing the transfer of SO(3)(-) to UDP-
32 revalent in the understudied polychlorinated sulfolipid class of natural products.
33                        Despite the fact that sulfolipids comprise a mere 4-7% of total leaf lipids, a
34             Along with phosphatidylglycerol, sulfolipid contributes to maintaining a negatively charg
35                                              Sulfolipid deficiency in pks2 mutant was confirmed by tw
36                                    With this sulfolipid-deficient mutant, it should be possible to te
37 ine phosphatase activity and substitution of sulfolipids for phospholipids, which are both indicators
38 s, flavonoids, peptides, fatty acids/amides, sulfolipids, glucosinolates and carotenoids.
39 inovosidases (SQases), which release SQ from sulfolipid glycoconjugates, so SQ can enter catabolism p
40                                              Sulfolipid-I (SL-I) is an abundant metabolite found in t
41  gene in Arabidopsis led to complete lack of sulfolipid in the respective sqd2 mutant.
42 nd quantify phospholipids, galactolipids and sulfolipids in sap using mass spectrometry.
43  environmental genome showed that the use of sulfolipids in subtropical gyres was confined primarily
44  test for the postulated important roles for sulfolipids in the pathogenesis of M. tuberculosis.
45                    Unlike the galactolipids, sulfolipid is anionic at physiological pH because of its
46  cavity in the cyanobacterial complex, and a sulfolipid is bound in the algal complex at a position c
47  were higher, while phosphatidylglycerol and sulfolipid levels were lower than in mature leaves, cons
48             Recently, we described synthetic sulfolipids named Sulfavants as a novel class of molecul
49 rolyze sulfate esters in glycosaminoglycans, sulfolipids, or steroid sulfates, thereby playing key ro
50 substrate for sulfotransferases that produce sulfolipids, putative virulence factors, in Mycobacteriu
51 s strain showed that the synthesis of mature sulfolipid SL-1 was interrupted and that a more polar su
52 lucose) is the polar head group of the plant sulfolipid SQ-diacylglycerol, and SQ comprises a major p
53                                          The sulfolipid sulfoquinovosyl diacylglycerol (SQDG), produc
54 thetic organisms and is the headgroup of the sulfolipid sulfoquinovosyl diacylglycerol.
55 ad group of plant, algal, and cyanobacterial sulfolipids: sulfoquinovosyl diacylglycerols.
56  revealed an increase in the dipalmitic acid sulfolipid sulfoquinovosyldiacylglycerol (SQDG), a chlor
57 d major anionic lipid in chloroplasts is the sulfolipid sulfoquinovosyldiacylglycerol (SQDG).
58                                          The sulfolipid sulfoquinovosyldiacylglycerol is a component
59                                          The sulfolipid sulfoquinovosyldiacylglycerol is one of the t
60                                          The sulfolipid sulfoquinovosyldiacylglycerol is present in t
61 th standards and served as substrate for the sulfolipid synthase associated with spinach chloroplast
62 942 is proposed to encode the cyanobacterial sulfolipid synthase catalyzing the last reaction of the
63 ethyl-branched fatty acids normally found in sulfolipids that is translocated to the cell surface.
64 protein Sap and MmpL8 are both essential for sulfolipid transport.
65  is potentiated by the previously identified sulfolipid transporter MmpL8.
66 , fatty acids, in addition to a new class of sulfolipids were annotated for the first time in Moringa
67 mmon plant phospholipids, but only traces of sulfolipids, with total lipid concentrations in extracte