Demange P, Bateman A, Mertz C, Dell A, Piémont Y, Abdallah M A
URA 31 CNRS, Département de Chimie, Université Louis Pasteur, Strasbourg, France.
Biochemistry. 1990 Dec 18;29(50):11041-51. doi: 10.1021/bi00502a005.
Pyoverdins were isolated and characterized respectively from the cultures of Pseudomonas tolaasii NCPPB 2192 (pyoverdins Pt, Pt A, and Pt B) and Pseudomonas fluorescens CCM 2798 (Pyoverdins Pf/1, Pf/2, Pf, Pf/3/1, and Pf/3/2) each grown in iron-deficient conditions. Their structures were established by using FAB-MS, NMR, and CD techniques. These siderophores are chromopeptides, and all but one (pyoverdin Pf/3/3) possess at the N-terminal end of their peptide chain the same chromophore that has been reported in pyoverdin Pa from Pseudomonas aeruginosa ATCC 15692 [Wendenbaum, S., Demange, P., Dell, A., Meyer, J. M., & Abdallah, M. A. (1983) Tetrahedron Lett. 24, 4877-4880] and pseudobactin B 10 from Pseudomonas B10 [Teintze, M., Hossain, M. B., Barnes, C. L., Leong, J., & Van der Helm, D. (1981) Biochemistry 20, 6446-6457] which is derived from 2,3-diamino-6,7-dihydroxyquinoline. In pyoverdins Pt this chromophore is bound to a linear peptide chain D-Ser-L-Lys-L-Ser-D-Ser-L-Thr-D-Ser-L-OHOrn-L-Thr-D-Ser-D-OHOrn (cyclic) which has its C-terminal end blocked by cyclic D-N delta-hydroxyornithine. In pyoverdins Pf, the peptide chain is also linear, SerCTHPMD-Gly-L-Ser-D-threo-OHAsp-L-Ala-Gly-D-Ala-Gly-L-O HOrn(cyclic), and contains an unusual natural amino acid which is the result of the condensation of 1 mol of serine and 1 mol of 2,4-diaminobutyric acid, forming a cyclic amidine. The pyoverdins Pt differ only in substituent bound to the nitrogen on C-3 of the chromophore, which is succinic acid in pyoverdin Pt A, succinamide in pyoverdin Pt, and alpha-ketoglutaric acid bound to the chromophore by its C-5 carbon atom in pyoverdin Pt B. Similarly, pyoverdin Pf/1, pyoverdin Pf/2, pyoverdin Pf (the major compound), and pyoverdin Pf/3/2 are substituted respectively by L-malic acid, succinic acid, L-malic amide, and succinamide. Pyoverdin Pf/3/3 has the same chromophore as azotobactin, the peptidic siderophore of Azotobacter vinelandii. These pyoverdins are very similar to pseudobactin B 10, the siderophore of Pseudomonas B10: they are linear peptides containing three bidentate groups strongly chelating Fe(III) and blocked at their N-terminal end by the catecholic chromophore and at their C-terminal end by cyclic N delta-hydroxyornithine. They differ therefore from other pyoverdins such as those from P. aeruginosa ATCC 15692 which contain a partly cyclic peptide [Briskot, G., Taraz, K., & Budzikiewicz, H. (1989) Liebigs Ann. Chem., 375-384].
分别从在缺铁条件下培养的托拉斯假单胞菌NCPPB 2192(绿脓菌素Pt、Pt A和Pt B)和荧光假单胞菌CCM 2798(绿脓菌素Pf/1、Pf/2、Pf、Pf/3/1和Pf/3/2)的培养物中分离并鉴定了绿脓菌素。通过使用快原子轰击质谱(FAB-MS)、核磁共振(NMR)和圆二色性(CD)技术确定了它们的结构。这些铁载体是色肽,除一种(绿脓菌素Pf/3/3)外,所有色肽在其肽链的N末端都具有与铜绿假单胞菌ATCC 15692的绿脓菌素Pa [温登鲍姆,S.,德芒热,P.,戴尔,A.,迈耶,J. M.,& 阿卜杜拉,M. A.(1983年)《四面体快报》24,4877 - 4880]和假单胞菌B10的假杆菌素B 10 [泰因策,M.,侯赛因,M. B.,巴恩斯,C. L.,梁,J.,& 范德赫尔姆,D.(1981年)《生物化学》20,6446 - 6457]中报道的相同发色团,该发色团衍生自2,3 - 二氨基 - 6,7 - 二羟基喹啉。在绿脓菌素Pt中,该发色团与线性肽链D - 丝氨酸 - L - 赖氨酸 - L - 丝氨酸 - D - 丝氨酸 - L - 苏氨酸 - D - 丝氨酸 - L - OHOrn - L - 苏氨酸 - D - 丝氨酸 - D - OHOrn(环状)相连,其C末端被环状D - Nδ - 羟基鸟氨酸封闭。在绿脓菌素Pf中,肽链也是线性的,SerCTHPMD - 甘氨酸 - L - 丝氨酸 - D - 苏式 - OHAsp - L - 丙氨酸 - 甘氨酸 - D - 丙氨酸 - 甘氨酸 - L - OHOrn(环状),并且包含一种不寻常的天然氨基酸,它是1摩尔丝氨酸和1摩尔2,4 - 二氨基丁酸缩合的产物,形成一个环状脒。绿脓菌素Pt仅在与发色团C - 3位氮原子相连的取代基上有所不同,在绿脓菌素Pt A中是琥珀酸,在绿脓菌素Pt中是琥珀酰胺,在绿脓菌素Pt B中是α - 酮戊二酸通过其C - 5碳原子与发色团相连。同样,绿脓菌素Pf/1、绿脓菌素Pf/2、绿脓菌素Pf(主要化合物)和绿脓菌素Pf/3/2分别被L - 苹果酸、琥珀酸、L - 苹果酰胺和琥珀酰胺取代。绿脓菌素Pf/3/3具有与棕色固氮菌肽铁载体偶氮菌素相同的发色团。这些绿脓菌素与假单胞菌B10的铁载体假杆菌素B 10非常相似:它们是线性肽,含有三个强螯合Fe(III)的双齿基团,在其N末端被儿茶酚发色团封闭,在其C末端被环状Nδ - 羟基鸟氨酸封闭。因此,它们与其他绿脓菌素不同,例如来自铜绿假单胞菌ATCC 15692的那些绿脓菌素,后者含有部分环状肽[布里斯科特,G.,塔拉兹,K.,& 布齐基维茨,H.(1989年)《利比希化学纪事》,375 - 384]。