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Pheophytin

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In photosystem II, pheophytin plays a very similar role. It again acts as the first electron carrier intermediate in the photosystem. After P680 becomes excited to P680, it transfers an electron to pheophytin, which converts the molecule into a negatively charged radical. Two negatively charged
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and plastoquinone (Klimov, Allakhverdiev, Klevanik, Shuvalov). This discovery was met with fierce opposition, since many believed pheophytin to only be a byproduct of chlorophyll degradation. Therefore, more experiments ensued to prove that pheophytin is indeed the primary electron acceptor of
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molecule and leaves photosystem II. The reactions outlined above in the section concerning purple bacteria give a general illustration of the actual movement of the electrons through pheophytin and the photosystem. The overall scheme is:
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Pheophytin is the first electron carrier intermediate in the photoreaction center (RC P870) of purple bacteria. Its involvement in this system can be broken down into 5 basic steps. The first step is excitation of the
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passing an electron to pheophytin, producing a negatively charged radical (the pheophytin) and a positively charged radical (the special pair of chlorophylls), which results in a charge separation.
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Xiong, Ling, and Richard Sayre. "The Identification of Potential Pheophytin Binding Sites in the Photosystem II Reaction Center of Chlamydomondas by Site-Directed Mutagenesis." (2000).
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Klimov VV (2003). "Discovery of pheophytin function in the photosynthetic energy conversion as the primary electron acceptor of Photosystem II".
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pheophytin radicals quickly pass their extra electrons to two consecutive plastoquinone molecules. Eventually, the electrons pass through the
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In 1977, scientists Klevanik, Klimov, Shuvalov performed a series of experiments to demonstrate that it is pheophytin and not
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PSII, occurring between P680 and plastoquinone (Klimov, Allakhverdiev, Shuvalov). The data that was obtained is as follows:
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Photo-reduction of pheophytin occurs at temperatures as low as 100K, and is observed after the reduction of plastoquinone.
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The fifth and final step involves the filling of the “hole” in the special pair by an electron from a heme in cytochrome
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Photo-reduction of pheophytin has been observed in various mixtures containing PSII reaction centers.
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that serves as the primary electron acceptor in photosystem II. Using several experiments, including
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These observations are all characteristic of photo-conversions of reaction center components.
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molecule lacking a central Mg ion. It can be produced from chlorophyll by treatment with a
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The quantity of pheophytin is in direct proportion to the number of PSII reaction centers.
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or the special pair of chlorophylls. This can be seen in the following reaction.
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The third step is the rapid electron movement to the tightly bound menaquinone, Q
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Definition of pheo in The American Heritage Stedman's Medical Dictionary
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Merriam-Webster Medical Dictionary definition of Pheophytin
330: 151: 114:, producing a dark bluish waxy pigment. The probable 384: 435:http://dictionary.reference.com/browse/pheophytin 961: 389:(4th ed.). Redondo Beach, CA: Plycon Press. 269: 27:Chlorophyll molecules lacking a central Mg2+ ion 172: 766: 483: 447:http://dictionary.reference.com/browse/pheo- 497: 490: 476: 394:Nelson, David L.; Cox, Michael M. (2005). 347: 398:(4th ed.). New York: W. H. Freeman. 137: 29: 14: 962: 106:In biochemical terms, pheophytin is a 471: 387:Illustrated Guide to Food Preparation 396:Lehninger Principles of Biochemistry 230:). Two electron transfers convert Q 415:America Society of Plant Biologists 408:Library of 3-D Molecular Structures 24: 202:The second step involves the (Chl) 118:comes from this description, with 25: 986: 404:Photosynthetic Molecules Section. 77:, and the type II photosynthetic 421: 148:electron paramagnetic resonance 452: 440: 428: 13: 1: 385:McWilliams, Margaret (1982). 341: 270:Involvement in photosystem II 218:+ ·Pheo (charge separation) 101: 7: 304: 173:Reaction in purple bacteria 10: 991: 300:Regeneration of substrates 931: 908: 887: 812: 757: 727: 664: 655: 627: 618: 577: 564: 555: 517: 506: 67:electron transfer pathway 61:that serves as the first 704:Magnesium protoporphyrin 970:Photosynthetic pigments 362:10.1023/A:1024990408747 297:Plastoquinone reduction 234:to its reduced form (Q 46: 804:Protoporphyrinogen IX 138:History and discovery 33: 897:Bacteriochlorophyll 876:Bacteriochlorophyll 180:bacteriochlorophylls 65:intermediate in the 910:Isobacteriochlorins 745:Protochlorophyllide 719:Zinc protoporphyrin 258:(quinone reduction) 81:(RC P870) found in 45:without the Mg ion. 790:Coproporphyrinogen 194:+ 1 photon → (Chl) 47: 957: 956: 953: 952: 949: 948: 753: 752: 709:Protoporphyrin IX 637:Adenosylcobalamin 614: 613: 610: 609: 587:Phycoerythrobilin 294:Charge separation 59:chemical compound 16:(Redirected from 982: 923:Sirohydrochlorin 889:Bacteriochlorins 776:Uroporphyrinogen 764: 763: 662: 661: 625: 624: 569:Phytochromobilin 562: 561: 515: 514: 492: 485: 478: 469: 468: 462: 456: 450: 444: 438: 432: 399: 390: 381: 63:electron carrier 21: 990: 989: 985: 984: 983: 981: 980: 979: 960: 959: 958: 945: 927: 904: 883: 808: 759: 749: 729:Phytoporphyrins 723: 666:Protoporphyrins 651: 647:Methylcobalamin 606: 602:Phycoviolobilin 592:Phycocyanobilin 573: 551: 532:Stercobilinogen 510: 502: 496: 466: 465: 457: 453: 445: 441: 433: 429: 424: 417:. 22 Apr. 2007. 410:. 22 April 2007 356:(1–3): 247–53. 350:Photosynth. Res 344: 326:Reaction center 307: 283: 272: 257: 253: 249: 246:2·Pheo + 2H + Q 241: 237: 233: 229: 225: 217: 214:+ Pheo → ·(Chl) 213: 205: 197: 193: 185: 175: 140: 104: 92: 83:purple bacteria 79:reaction center 28: 23: 22: 15: 12: 11: 5: 988: 978: 977: 972: 955: 954: 951: 950: 947: 946: 944: 943: 937: 935: 929: 928: 926: 925: 920: 914: 912: 906: 905: 903: 902: 893: 891: 885: 884: 882: 881: 873: 855: 837: 822:Chlorophyllide 818: 816: 810: 809: 807: 806: 801: 787: 772: 770: 768:Porphyrinogens 761: 755: 754: 751: 750: 748: 747: 742: 733: 731: 725: 724: 722: 721: 716: 711: 706: 701: 670: 668: 659: 653: 652: 650: 649: 644: 642:Cyanocobalamin 639: 633: 631: 622: 616: 615: 612: 611: 608: 607: 605: 604: 599: 594: 589: 583: 581: 575: 574: 572: 571: 565: 559: 553: 552: 550: 549: 544: 539: 534: 529: 524: 518: 512: 504: 503: 495: 494: 487: 480: 472: 464: 463: 451: 439: 426: 425: 423: 420: 419: 418: 411: 400: 391: 382: 343: 340: 339: 338: 336:Chlorophyllide 333: 328: 323: 318: 313: 311:Photosynthesis 306: 303: 302: 301: 298: 295: 292: 281: 271: 268: 260: 259: 255: 251: 247: 239: 235: 231: 227: 223: 220: 219: 215: 211: 203: 200: 199: 195: 191: 183: 174: 171: 167: 166: 163: 160: 139: 136: 103: 100: 99: 98: 97:to each other. 90: 71:Photosystem II 26: 9: 6: 4: 3: 2: 987: 976: 975:Tetrapyrroles 973: 971: 968: 967: 965: 942: 941:Cofactor F430 939: 938: 936: 934: 930: 924: 921: 919: 916: 915: 913: 911: 907: 901: 900: 895: 894: 892: 890: 886: 880: 879: 874: 871: 870: 865: 864: 859: 856: 853: 852: 847: 846: 841: 838: 835: 834: 829: 828: 823: 820: 819: 817: 815: 811: 805: 802: 799: 795: 791: 788: 785: 781: 777: 774: 773: 771: 769: 765: 762: 756: 746: 743: 741: 740: 735: 734: 732: 730: 726: 720: 717: 715: 712: 710: 707: 705: 702: 699: 698: 693: 692: 687: 686: 681: 680: 675: 672: 671: 669: 667: 663: 660: 658: 654: 648: 645: 643: 640: 638: 635: 634: 632: 630: 626: 623: 621: 617: 603: 600: 598: 597:Phycourobilin 595: 593: 590: 588: 585: 584: 582: 580: 576: 570: 567: 566: 563: 560: 558: 554: 548: 545: 543: 540: 538: 535: 533: 530: 528: 525: 523: 520: 519: 516: 513: 509: 505: 501: 500:tetrapyrroles 493: 488: 486: 481: 479: 474: 473: 470: 460: 455: 448: 443: 436: 431: 427: 416: 412: 409: 405: 401: 397: 392: 388: 383: 379: 375: 371: 367: 363: 359: 355: 351: 346: 345: 337: 334: 332: 329: 327: 324: 322: 319: 317: 314: 312: 309: 308: 299: 296: 293: 290: 289: 288: 285: 278: 267: 265: 245: 244: 243: 209: 208: 207: 189: 188: 187: 181: 170: 164: 161: 158: 157: 156: 153: 149: 145: 144:plastoquinone 135: 133: 129: 125: 121: 117: 113: 109: 96: 88: 84: 80: 76: 72: 68: 64: 60: 56: 52: 49: 48: 44: 43: 37: 32: 19: 898: 877: 868: 862: 857: 850: 844: 832: 826: 738: 737:Chlorophyll 696: 690: 684: 678: 542:Urobilinogen 454: 442: 430: 414: 407: 395: 386: 353: 349: 279: 273: 263: 261: 221: 201: 198:(excitation) 176: 168: 141: 131: 127: 123: 119: 105: 94: 54: 50: 41: 40:chlorophyll 35: 840:Chlorophyll 579:Phycobilins 557:Phytobilins 537:Stercobilin 321:Chlorophyll 316:Photosystem 250:→ 2Pheo + Q 108:chlorophyll 73:(PS II) in 55:phaeophytin 34:Pheophytin 18:Phaeophytin 964:Categories 858:Pheophytin 760:porphyrins 714:Pterobilin 657:Porphyrins 629:Corrinoids 620:Macrocycle 527:Biliverdin 422:References 342:References 291:Excitation 277:cytochrome 132:vegetation 51:Pheophytin 522:Bilirubin 498:Types of 116:etymology 112:weak acid 102:Structure 95:analogous 933:Corphins 918:Siroheme 814:Chlorins 547:Urobilin 511:(Linear) 378:29278470 370:16228584 305:See also 130:meaning 122:meaning 758:Reduced 508:Bilanes 87:quinone 38:, i.e. 376:  368:  75:plants 374:S2CID 210:(Chl) 190:(Chl) 182:(Chl) 124:dusky 57:is a 674:Heme 459:phyt 366:PMID 331:P680 152:P680 128:phyt 126:and 120:pheo 798:III 784:III 358:doi 242:). 69:of 53:or 966:: 866:, 848:, 830:, 796:, 782:, 694:, 688:, 682:, 406:" 372:. 364:. 354:76 352:. 134:. 89:(Q 899:a 878:c 872:) 869:b 863:a 860:( 854:) 851:b 845:a 842:( 836:) 833:b 827:a 824:( 800:) 794:I 792:( 786:) 780:I 778:( 739:c 700:) 697:o 691:a 685:c 679:b 676:( 491:e 484:t 477:v 402:" 380:. 360:: 284:f 282:6 280:b 264:c 256:2 254:H 252:B 248:B 240:2 238:H 236:B 232:B 228:B 224:A 216:2 212:2 204:2 196:2 192:2 184:2 91:A 42:a 36:a 20:)

Index

Phaeophytin

chlorophyll a
chemical compound
electron carrier
electron transfer pathway
Photosystem II
plants
reaction center
purple bacteria
quinone
chlorophyll
weak acid
etymology
plastoquinone
electron paramagnetic resonance
P680
bacteriochlorophylls
cytochrome
Photosynthesis
Photosystem
Chlorophyll
Reaction center
P680
Chlorophyllide
doi
10.1023/A:1024990408747
PMID
16228584
S2CID

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