Polymyxin-resistant mutants of Escherichia coli and Salmonella typhimurium accumulate a novel minor lipid that can donate 4-amino-4-deoxy-l-arabinose units (l-Ara4N) to lipid A. We now report the purification of this lipid from a pss(-) pmrA(C) mutant of E. coli and assign its structure as undecaprenyl phosphate-α-L-Ara4N. Approximately 0.2 mg of homogeneous material was isolated from an 8-liter culture by solvent extraction, followed by chromatography on DEAE-cellulose, C18 reverse phase resin, and silicic acid. Matrix-assisted laser desorption ionization/time of flight mass spectrometry in the negative mode yielded a single species [M - H](-) at m/z 977.5, consistent with undecaprenyl phosphate-α-L-Ara4N (M(r) = 978.41). (31)P NMR spectroscopy showed a single phosphorus atom at -0.44 ppm characteristic of a phosphodiester linkage. Selective inverse decoupling difference spectroscopy demonstrated that the undecaprenyl phosphate group is attached to the anomeric carbon of the l-Ara4N unit. One- and two-dimensional (1)H NMR studies confirmed the presence of a polyisoprene chain and a sugar moiety with chemical shifts and coupling constants expected for an equatorially substituted arabinopyranoside. Heteronuclear multiple-quantum coherence spectroscopy analysis demonstrated that a nitrogen atom is attached to C-4 of the sugar residue. The purified donor supports in vitro conversion of lipid IV(A) to lipid II(A), which is substituted with a single l-Ara4N moiety. The identification of undecaprenyl phosphate-α-L-Ara4N implies that l-Ara4N transfer to lipid A occurs in the periplasm of polymyxin-resistant strains, and establishes a new enzymatic pathway by which Gram-negative bacteria acquire antibiotic resistance.

Escherichia coli, lipid A, polymyxin-resistant mutants, Salmonella typhimurium

13C NMR data:
Linkage	Residue	C1	C2	C3	C4	C5
1,0	aLArap4N	99.5	72.4	70.8	51.0	63.0
1	P
	Und


1H NMR data:
Linkage	Residue	H1	H2	H3	H4	H5
1,0	aLArap4N	4.902	3.611	3.810	3.292	3.709-3.955
1	P
	Und


1H/13C HSQC data:
Linkage	Residue	C1/H1	C2/H2	C3/H3	C4/H4	C5/H5
1,0	aLArap4N	99.5/4.902	72.4/3.611	70.8/3.810	51.0/3.292	63.0/3.709-3.955
1	P
	Und

There is only one chemically distinct structure:

SVGMWSMILES3D molIonize

 

CCCCCCCCCCCOP(=O)(O)O[C@@H]1OC[C@H](N)[C@H](O)[C@H]1O

383.422 g/mol (C₁₆H₃₄NO₇P)