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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
319: 140: 103:, producing a dark bluish waxy pigment. The probable 373: 424:http://dictionary.reference.com/browse/pheophytin 950: 378:(4th ed.). Redondo Beach, CA: Plycon Press. 258: 16:Chlorophyll molecules lacking a central Mg2+ ion 161: 755: 472: 436:http://dictionary.reference.com/browse/pheo- 486: 479: 465: 383:Nelson, David L.; Cox, Michael M. (2005). 336: 387:(4th ed.). New York: W. H. Freeman. 126: 18: 951: 95:In biochemical terms, pheophytin is a 460: 376:Illustrated Guide to Food Preparation 385:Lehninger Principles of Biochemistry 219:). Two electron transfers convert Q 404:America Society of Plant Biologists 397:Library of 3-D Molecular Structures 13: 191:The second step involves the (Chl) 107:comes from this description, with 14: 975: 393:Photosynthetic Molecules Section. 66:, and the type II photosynthetic 410: 137:electron paramagnetic resonance 441: 429: 417: 1: 374:McWilliams, Margaret (1982). 330: 259:Involvement in photosystem II 207:+ ·Pheo (charge separation) 90: 7: 293: 162:Reaction in purple bacteria 10: 980: 289:Regeneration of substrates 920: 897: 876: 801: 746: 716: 653: 644: 616: 607: 566: 553: 544: 506: 495: 56:electron transfer pathway 50:that serves as the first 693:Magnesium protoporphyrin 959:Photosynthetic pigments 351:10.1023/A:1024990408747 286:Plastoquinone reduction 223:to its reduced form (Q 35: 793:Protoporphyrinogen IX 127:History and discovery 22: 886:Bacteriochlorophyll 865:Bacteriochlorophyll 169:bacteriochlorophylls 54:intermediate in the 899:Isobacteriochlorins 734:Protochlorophyllide 708:Zinc protoporphyrin 247:(quinone reduction) 70:(RC P870) found in 34:without the Mg ion. 779:Coproporphyrinogen 183:+ 1 photon → (Chl) 36: 946: 945: 942: 941: 938: 937: 742: 741: 698:Protoporphyrin IX 626:Adenosylcobalamin 603: 602: 599: 598: 576:Phycoerythrobilin 283:Charge separation 48:chemical compound 971: 912:Sirohydrochlorin 878:Bacteriochlorins 765:Uroporphyrinogen 753: 752: 651: 650: 614: 613: 558:Phytochromobilin 551: 550: 504: 503: 481: 474: 467: 458: 457: 451: 445: 439: 433: 427: 421: 388: 379: 370: 52:electron carrier 979: 978: 974: 973: 972: 970: 969: 968: 949: 948: 947: 934: 916: 893: 872: 797: 748: 738: 718:Phytoporphyrins 712: 655:Protoporphyrins 640: 636:Methylcobalamin 595: 591:Phycoviolobilin 581:Phycocyanobilin 562: 540: 521:Stercobilinogen 499: 491: 485: 455: 454: 446: 442: 434: 430: 422: 418: 413: 406:. 22 Apr. 2007. 399:. 22 April 2007 345:(1–3): 247–53. 339:Photosynth. Res 333: 315:Reaction center 296: 272: 261: 246: 242: 238: 235:2·Pheo + 2H + Q 230: 226: 222: 218: 214: 206: 203:+ Pheo → ·(Chl) 202: 194: 186: 182: 174: 164: 129: 93: 81: 72:purple bacteria 68:reaction center 17: 12: 11: 5: 977: 967: 966: 961: 944: 943: 940: 939: 936: 935: 933: 932: 926: 924: 918: 917: 915: 914: 909: 903: 901: 895: 894: 892: 891: 882: 880: 874: 873: 871: 870: 862: 844: 826: 811:Chlorophyllide 807: 805: 799: 798: 796: 795: 790: 776: 761: 759: 757:Porphyrinogens 750: 744: 743: 740: 739: 737: 736: 731: 722: 720: 714: 713: 711: 710: 705: 700: 695: 690: 659: 657: 648: 642: 641: 639: 638: 633: 631:Cyanocobalamin 628: 622: 620: 611: 605: 604: 601: 600: 597: 596: 594: 593: 588: 583: 578: 572: 570: 564: 563: 561: 560: 554: 548: 542: 541: 539: 538: 533: 528: 523: 518: 513: 507: 501: 493: 492: 484: 483: 476: 469: 461: 453: 452: 440: 428: 415: 414: 412: 409: 408: 407: 400: 389: 380: 371: 332: 329: 328: 327: 325:Chlorophyllide 322: 317: 312: 307: 302: 300:Photosynthesis 295: 292: 291: 290: 287: 284: 281: 270: 260: 257: 249: 248: 244: 240: 236: 228: 224: 220: 216: 212: 209: 208: 204: 200: 192: 189: 188: 184: 180: 172: 163: 160: 156: 155: 152: 149: 128: 125: 92: 89: 88: 87: 86:to each other. 79: 60:Photosystem II 15: 9: 6: 4: 3: 2: 976: 965: 964:Tetrapyrroles 962: 960: 957: 956: 954: 931: 930:Cofactor F430 928: 927: 925: 923: 919: 913: 910: 908: 905: 904: 902: 900: 896: 890: 889: 884: 883: 881: 879: 875: 869: 868: 863: 860: 859: 854: 853: 848: 845: 842: 841: 836: 835: 830: 827: 824: 823: 818: 817: 812: 809: 808: 806: 804: 800: 794: 791: 788: 784: 780: 777: 774: 770: 766: 763: 762: 760: 758: 754: 751: 745: 735: 732: 730: 729: 724: 723: 721: 719: 715: 709: 706: 704: 701: 699: 696: 694: 691: 688: 687: 682: 681: 676: 675: 670: 669: 664: 661: 660: 658: 656: 652: 649: 647: 643: 637: 634: 632: 629: 627: 624: 623: 621: 619: 615: 612: 610: 606: 592: 589: 587: 586:Phycourobilin 584: 582: 579: 577: 574: 573: 571: 569: 565: 559: 556: 555: 552: 549: 547: 543: 537: 534: 532: 529: 527: 524: 522: 519: 517: 514: 512: 509: 508: 505: 502: 498: 494: 490: 489:tetrapyrroles 482: 477: 475: 470: 468: 463: 462: 459: 449: 444: 437: 432: 425: 420: 416: 405: 401: 398: 394: 390: 386: 381: 377: 372: 368: 364: 360: 356: 352: 348: 344: 340: 335: 334: 326: 323: 321: 318: 316: 313: 311: 308: 306: 303: 301: 298: 297: 288: 285: 282: 279: 278: 277: 274: 267: 256: 254: 234: 233: 232: 198: 197: 196: 178: 177: 176: 170: 159: 153: 150: 147: 146: 145: 142: 138: 134: 133:plastoquinone 124: 122: 118: 114: 110: 106: 102: 98: 85: 77: 73: 69: 65: 61: 57: 53: 49: 45: 41: 38: 37: 33: 32: 26: 21: 887: 866: 857: 851: 846: 839: 833: 821: 815: 727: 726:Chlorophyll 685: 679: 673: 667: 531:Urobilinogen 443: 431: 419: 403: 396: 384: 375: 342: 338: 268: 262: 252: 250: 210: 190: 187:(excitation) 165: 157: 130: 120: 116: 112: 108: 94: 83: 43: 39: 30: 29:chlorophyll 24: 829:Chlorophyll 568:Phycobilins 546:Phytobilins 526:Stercobilin 310:Chlorophyll 305:Photosystem 239:→ 2Pheo + Q 97:chlorophyll 62:(PS II) in 44:phaeophytin 23:Pheophytin 953:Categories 847:Pheophytin 749:porphyrins 703:Pterobilin 646:Porphyrins 618:Corrinoids 609:Macrocycle 516:Biliverdin 411:References 331:References 280:Excitation 266:cytochrome 121:vegetation 40:Pheophytin 511:Bilirubin 487:Types of 105:etymology 101:weak acid 91:Structure 84:analogous 922:Corphins 907:Siroheme 803:Chlorins 536:Urobilin 500:(Linear) 367:29278470 359:16228584 294:See also 119:meaning 111:meaning 747:Reduced 497:Bilanes 76:quinone 27:, i.e. 365:  357:  64:plants 363:S2CID 199:(Chl) 179:(Chl) 171:(Chl) 113:dusky 46:is a 663:Heme 448:phyt 355:PMID 320:P680 141:P680 117:phyt 115:and 109:pheo 787:III 773:III 347:doi 231:). 58:of 42:or 955:: 855:, 837:, 819:, 785:, 771:, 683:, 677:, 671:, 395:" 361:. 353:. 343:76 341:. 123:. 78:(Q 888:a 867:c 861:) 858:b 852:a 849:( 843:) 840:b 834:a 831:( 825:) 822:b 816:a 813:( 789:) 783:I 781:( 775:) 769:I 767:( 728:c 689:) 686:o 680:a 674:c 668:b 665:( 480:e 473:t 466:v 391:" 369:. 349:: 273:f 271:6 269:b 253:c 245:2 243:H 241:B 237:B 229:2 227:H 225:B 221:B 217:B 213:A 205:2 201:2 193:2 185:2 181:2 173:2 80:A 31:a 25:a

Index


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
29278470

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