Knowledge

Gibberellic acid

Source 📝

373: 260: 51: 533: 42: 605: 694:. Gibberellic acid is a very potent hormone whose natural occurrence in plants controls their development. Since GA regulates growth, applications of very low concentrations can have a profound effect while too much will have the opposite effect. It is usually used in concentrations between 0.01 and 10 mg/L. 875:
Camara, M. C. et al (2015) General Aspects and Applications of Gibberelins and Gibberellic Acid in Plants. In: Hardy, J.. (Org.). Gibberellins and Gibberellic Acid: Biosynthesis, Regulation and Physiological Effects. 1ed.Hauppauge: Nova Science Publishers, 2015, v., p.
760:
in the cherry industry. It is used on Clementine Mandarin oranges, which may otherwise cross-pollinate with other citrus and produce undesirable seeds. Applied directly on the blossoms as a spray, it allows for Clementines to produce a full crop of seedless fruit.
145: 685:
acid promoting growth and elongation of cells. It affects decomposition of plants and helps plants grow if used in small amounts, but eventually plants develop tolerance to it. GA stimulates the cells of germinating seeds to produce
541: 513: 789:
industry. A GA solution is sprayed on the barley after the steeping process is completed. This stimulates growth in otherwise partly dormant kernels and produces a uniform and rapid growth.
583: 396:
InChI=1S/C19H22O6/c1-9-7-17-8-18(9,24)5-3-10(17)19-6-4-11(20)16(2,15(23)25-19)13(19)12(17)14(21)22/h4,6,10-13,20,24H,1,3,5,7-8H2,2H3,(H,21,22)/t10-,11+,12-,13-,16+,17+,18+,19-/m1/s1
406:
InChI=1/C19H22O6/c1-9-7-17-8-18(9,24)5-3-10(17)19-6-4-11(20)16(2,15(23)25-19)13(19)12(17)14(21)22/h4,6,10-13,20,24H,1,3,5,7-8H2,2H3,(H,21,22)/t10-,11+,12-,13-,16+,17+,18+,19-/m1/s1
841:"Gibberellic acid fermented extract obtained by solid-state fermentation using citric pulp by Fusarium moniliforme: Influence on Lavandula angustifolia Mill. cultivated in vitro" 618: 966: 674:
Plants in their normal state produce large amounts of GA3. It is possible to produce the hormone industrially using microorganisms. Gibberellic acid is a simple
1028: 422: 744:. It is also widely used in the grape-growing industry as a hormone to induce the production of larger bunches and bigger grapes, especially 387: 1038: 1033: 890: 579: 569: 330: 778:'Variegatum' kept in water is about 7 days. To extend their life after cutting, conditioning with gibberellic acid or 717:("foolish seedling"), which causes them to rapidly elongate beyond their normal adult height. The plants subsequently 351: 532: 1018: 625: 724:
Gibberellins have a number of effects on plant development. They can stimulate rapid stem and root growth, induce
267: 587: 1008: 774: 255: 99:)-7,12-Dihydroxy-3-methyl-6-methylene-2-oxoperhydro-4a,7-methano-9b,3-propenoazulenofuran-4-carboxylic acid 1013: 197: 718: 555: 525: 63: 50: 839:
Silva ALL, Rodrigues C, Costa JL, Machado MP, Penha RO, Biasi LA, Vandenberghe LPS, Soccol CR (2013).
699: 814: 679: 368: 111: 157: 1023: 947: 217: 982: 937: 929: 725: 656: 497: 445: 339: 745: 697:
GA was first identified in Japan in 1926, as a metabolic by-product of the plant pathogen
372: 259: 177: 121: 753: 596: 942: 917: 1002: 809: 798: 779: 757: 687: 652: 486: 248: 736:
Gibberellic acid is sometimes used in laboratory and greenhouse settings to trigger
575: 319: 965:
Krzymińska-Bródka A, Ulczycka-Walorska M, Łysiak GP, Czuchaj P (December 2023).
804: 737: 675: 28: 894: 840: 41: 17: 769: 473: 208: 561: 765: 691: 682: 951: 491:
233 to 235 °C (451 to 455 °F; 506 to 508 K) (decomposition)
749: 741: 228: 987: 933: 237: 786: 713: 306: 268: 764:
It can be used to extend the shelf life of flowers and cut greens in
188: 595:
Except where otherwise noted, data are given for materials in their
27:
This article is about the chemical. For its function in plants, see
728:
in the leaves of some plants, and increase seed germination rates.
294: 819: 168: 144: 134: 704: 285: 356: 613: 918:"Dormancy in Seeds of Charlock (Sinapis arvensis L.)" 891:"Gibberellic Acid for Fruit Set and Seed Germination" 671:. When purified, it is a white to pale-yellow solid. 971:(L.) All. shoots depending on postharvest handling" 318: 430:O=C1O52\C=C/(O)1(5(C(=O)O)432CC(O)(C(=C)C3)C4)C 120: 8: 782:is used. This doubles their possible use. 371: 258: 216: 33: 986: 941: 338: 871: 869: 884: 882: 831: 427: 392: 367: 236: 249: 740:in seeds that would otherwise remain 399:Key: IXORZMNAPKEEDV-SNTJWBGVSA-N 196: 176: 7: 1029:Heterocyclic compounds with 5 rings 409:Key: IXORZMNAPKEEDV-SNTJWBGVBW 309: 293: 981:. Polish Botanical Society: 1–11. 25: 721:due to lack of support, and die. 785:GA is widely used in the barley 703:(thus the name), which afflicts 603: 531: 457: 49: 40: 655:found in plants and fungi. Its 599:(at 25 °C , 100 kPa). 756:valleys, it is also used as a 463: 451: 1: 1055: 848:Pakistan Journal of Botany 26: 711:-infected plants develop 593: 512: 507: 438: 418: 383: 104: 62: 57: 48: 39: 916:Edwards, Miriam (1976). 690:molecules that code for 570:Precautionary statements 1039:Plant growth regulators 969:Polygonatum multiflorum 775:Polygonatum multiflorum 967:"The longevity of cut 1034:Vinylidene compounds 700:Gibberella fujikuroi 934:10.1104/pp.58.5.626 815:6-Benzylaminopurine 498:Solubility in water 481: g·mol 158:Beilstein Reference 36: 692:hydrolytic enzymes 626:Infobox references 34: 1019:Tertiary alcohols 988:10.5586/aa/176280 975:Acta Agrobotanica 772:of cut shoots of 746:Thompson seedless 634:Chemical compound 632: 631: 556:Hazard statements 352:CompTox Dashboard 146:Interactive image 35:Gibberellic acid 16:(Redirected from 1046: 993: 992: 990: 962: 956: 955: 945: 913: 907: 906: 904: 902: 893:. Archived from 886: 877: 873: 864: 863: 861: 859: 845: 836: 758:growth regulator 726:mitotic division 657:chemical formula 638:Gibberellic acid 616: 610: 607: 606: 589: 585: 581: 577: 563: 535: 480: 465: 459: 453: 446:Chemical formula 376: 375: 360: 358: 342: 322: 311: 297: 270: 262: 251: 240: 220: 200: 180: 148: 124: 53: 44: 37: 21: 1054: 1053: 1049: 1048: 1047: 1045: 1044: 1043: 999: 998: 997: 996: 964: 963: 959: 915: 914: 910: 900: 898: 897:on 3 March 2008 889:Riley, John M. 888: 887: 880: 874: 867: 857: 855: 843: 838: 837: 833: 828: 795: 748:grapes. In the 734: 670: 666: 662: 649: 635: 628: 623: 622: 621:  ?) 612: 608: 604: 600: 572: 558: 544: 528: 500: 478: 468: 462: 456: 448: 434: 431: 426: 425: 414: 411: 410: 407: 401: 400: 397: 391: 390: 379: 361: 354: 345: 325: 312: 300: 280: 243: 223: 203: 183: 160: 151: 138: 127: 114: 100: 32: 23: 22: 18:Gibberelic acid 15: 12: 11: 5: 1052: 1050: 1042: 1041: 1036: 1031: 1026: 1021: 1016: 1011: 1009:Plant hormones 1001: 1000: 995: 994: 957: 928:(5): 626–630. 908: 878: 865: 854:(6): 2057–2064 830: 829: 827: 824: 823: 822: 817: 812: 807: 802: 794: 791: 733: 730: 668: 664: 660: 647: 642:gibberellin A3 633: 630: 629: 624: 602: 601: 597:standard state 594: 591: 590: 584:P305+P351+P338 573: 568: 565: 564: 559: 554: 551: 550: 545: 540: 537: 536: 529: 524: 521: 520: 510: 509: 505: 504: 503:5 g/L (20 °C) 501: 496: 493: 492: 489: 483: 482: 476: 470: 469: 466: 460: 454: 449: 444: 441: 440: 436: 435: 433: 432: 429: 421: 420: 419: 416: 415: 413: 412: 408: 405: 404: 402: 398: 395: 394: 386: 385: 384: 381: 380: 378: 377: 364: 362: 350: 347: 346: 344: 343: 335: 333: 327: 326: 324: 323: 315: 313: 305: 302: 301: 299: 298: 290: 288: 282: 281: 279: 278: 274: 272: 264: 263: 253: 245: 244: 242: 241: 233: 231: 225: 224: 222: 221: 213: 211: 205: 204: 202: 201: 193: 191: 185: 184: 182: 181: 173: 171: 165: 164: 161: 156: 153: 152: 150: 149: 141: 139: 132: 129: 128: 126: 125: 117: 115: 110: 107: 106: 102: 101: 66: 60: 59: 55: 54: 46: 45: 24: 14: 13: 10: 9: 6: 4: 3: 2: 1051: 1040: 1037: 1035: 1032: 1030: 1027: 1025: 1022: 1020: 1017: 1015: 1014:Cyclohexenols 1012: 1010: 1007: 1006: 1004: 989: 984: 980: 976: 972: 970: 961: 958: 953: 949: 944: 939: 935: 931: 927: 923: 922:Plant Physiol 919: 912: 909: 896: 892: 885: 883: 879: 872: 870: 866: 853: 849: 842: 835: 832: 825: 821: 818: 816: 813: 811: 810:Plant hormone 808: 806: 803: 800: 799:Abscisic acid 797: 796: 792: 790: 788: 783: 781: 780:benzyladenine 777: 776: 771: 767: 762: 759: 755: 751: 747: 743: 739: 731: 729: 727: 722: 720: 716: 715: 710: 706: 702: 701: 695: 693: 689: 684: 681: 677: 672: 658: 654: 650: 643: 640:(also called 639: 627: 620: 615: 598: 592: 574: 571: 567: 566: 560: 557: 553: 552: 549: 546: 543: 539: 538: 534: 530: 527: 523: 522: 518: 516: 511: 506: 502: 499: 495: 494: 490: 488: 487:Melting point 485: 484: 477: 475: 472: 471: 450: 447: 443: 442: 437: 428: 424: 417: 403: 393: 389: 382: 374: 370: 369:DTXSID0020656 366: 365: 363: 353: 349: 348: 341: 337: 336: 334: 332: 329: 328: 321: 317: 316: 314: 308: 304: 303: 296: 292: 291: 289: 287: 284: 283: 276: 275: 273: 271: 266: 265: 261: 257: 254: 252: 250:ECHA InfoCard 247: 246: 239: 235: 234: 232: 230: 227: 226: 219: 215: 214: 212: 210: 207: 206: 199: 195: 194: 192: 190: 187: 186: 179: 175: 174: 172: 170: 167: 166: 162: 159: 155: 154: 147: 143: 142: 140: 136: 131: 130: 123: 119: 118: 116: 113: 109: 108: 103: 98: 94: 90: 86: 82: 78: 74: 70: 65: 61: 56: 52: 47: 43: 38: 30: 19: 978: 974: 968: 960: 925: 921: 911: 899:. Retrieved 895:the original 856:. Retrieved 851: 847: 834: 784: 773: 763: 735: 723: 712: 708: 698: 696: 673: 645: 641: 637: 636: 547: 514: 198:ChEMBL566653 105:Identifiers 96: 92: 88: 84: 80: 76: 72: 68: 858:26 November 805:Gibberellin 738:germination 680:pentacyclic 676:gibberellin 542:Signal word 439:Properties 256:100.000.911 178:CHEBI:28833 29:Gibberellin 1003:Categories 826:References 770:shelf life 526:Pictograms 474:Molar mass 340:BU0A7MWB6L 209:ChemSpider 133:3D model ( 112:CAS Number 64:IUPAC name 766:floristry 709:Fujikuroi 683:diterpene 588:P337+P313 517:labelling 277:201-001-0 269:EC Number 1024:Lactones 952:16659732 793:See also 750:Okanagan 707:plants. 508:Hazards 229:DrugBank 787:malting 754:Creston 742:dormant 714:bakanae 653:hormone 651:) is a 619:what is 617: ( 548:Warning 479:346.379 307:PubChem 238:DB07814 218:7995349 122:77-06-5 950:  943:542271 940:  901:26 Oct 768:. The 614:verify 611:  423:SMILES 295:C01699 189:ChEMBL 163:54346 58:Names 876:1-21. 844:(PDF) 820:Auxin 801:(ABA) 719:lodge 388:InChI 169:ChEBI 135:JSmol 948:PMID 903:2012 860:2014 752:and 732:Uses 705:rice 688:mRNA 678:, a 659:is C 580:P280 576:P264 562:H319 331:UNII 320:6466 286:KEGG 983:doi 938:PMC 930:doi 644:or 515:GHS 357:EPA 310:CID 95:,12 91:,9b 87:,9a 79:,4a 71:,3a 1005:: 979:76 977:. 973:. 946:. 936:. 926:58 924:. 920:. 881:^ 868:^ 852:45 850:. 846:. 665:22 661:19 646:GA 586:, 582:, 578:, 519:: 461:22 455:19 83:,7 75:,4 67:(3 991:. 985:: 954:. 932:: 905:. 862:. 669:6 667:O 663:H 648:3 609:N 467:6 464:O 458:H 452:C 359:) 355:( 137:) 97:S 93:R 89:R 85:S 81:S 77:S 73:S 69:S 31:. 20:)

Index

Gibberelic acid
Gibberellin


IUPAC name
CAS Number
77-06-5
JSmol
Interactive image
Beilstein Reference
ChEBI
CHEBI:28833
ChEMBL
ChEMBL566653
ChemSpider
7995349
DrugBank
DB07814
ECHA InfoCard
100.000.911
Edit this at Wikidata
EC Number
KEGG
C01699
PubChem
6466
UNII
BU0A7MWB6L
CompTox Dashboard
DTXSID0020656

Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.