Knowledge

Arabinoxylan

Source 📝

106:
Due to its importance in food, the structure of arabinoxylan from wheat grain and other cereals has been intensively studied. In particular, the arabinoxylan from wheat endosperm that gives rise to white flour has a simpler structure than that from most tissues. Apart from the structural features
90:
As with all xylan, the backbone of arabinoxylan chains is composed of a large number of 1,4-linked β-D-xylopyranosyl units. In arabinoxylan many of these xylose units are 3-linked with single α-L-arabinofuranosyl units and some of these arabinose in turn have ester-linked ferulic acid residues.
127:
and others. These acylated arabinosyl residues are frequently additionally substituted with 2-linked sugars. In lignified cell walls, there is strong evidence that feruloyl residues on arabinoxylan can be crosslinked into the lignin polymer, increasing recalcitrance to digestion.
118:
resides and other sugars and these arabinoxylan polymers are sometimes termed glucuronarabinoxylans or heteroxylans. Both backbone and sidechain sugar residues can be acetylated. Arabinosyl residues can be acylated with phenolics other than ferulic acid, in particular
69:
between arabinoxylan chains and with lignin. Whilst arabinose has been found linked to xylan in non-commelinid plants, ferulic acid has not been reported on these and unlike feruloyl-arabinoxylan these arabinoxylans are not
291:
Dervilly-Pinel, G; et al. (2004). "Investigation of the distribution of arabinose residues on the xylan backbone of water-soluble arabinoxylans from wheat flour".
111:
residues. Due to a low degree of crosslinking into the cell wall, some of this endosperm arabinoxylan is extractable in water, giving rise to soluble dietary fiber.
95:
and possibly higher oligomers that covalently crosslink arabinoxylan chains. This mode of cross-linking is a key feature of both primary and secondary cell walls in
235:
Marcotuli, Ilaria; Hsieh, Yves S.-Y.; Lahnstein, Jelle; Yap, Kuok; Burton, Rachel Anita; Blanco, Antonio; Fincher, Geoffrey Bruce; Gadaleta, Agata (13 April 2016).
354:
Rao, RS; Muralikrishna, G (2006). "Water soluble feruloyl arabinoxylans from rice and ragi: changes upon malting and their consequence on antioxidant activity".
327:
Izydorczyk, MS; Dexter, JE (2008). "Barley β-glucans and arabinoxylans: Molecular structure, physicochemical properties, and uses in food products–a Review".
389:
Guillon, F; Champ, M (2000). "Structural and physical properties of dietary fibres, and consequences of processing on human physiology".
163:
which are shown to exert various health benefits. In addition, arabinoxylans, owing to their bound phenolic acids, are shown to have
184: 114:
Arabinoxylans from tissues other than endosperm are structurally more complex. The xylan backbone is often heavily substituted with
167:
activity. Their ion exchange capacity and viscosity are also partly responsible for their beneficial metabolic effects.
223: 237:"Structural Variation and Content of Arabinoxylans in Endosperm and Bran of Durum Wheat ( Triticum turgidum L.)" 58: 92: 422: 8: 427: 192: 236: 402: 371: 266: 152:
to them. Phenolic acids may also be involved in defense including protection against
367: 398: 363: 336: 300: 256: 248: 74:. The remainder of this article refers to feruloyl-arabinoxylan from cell walls of 340: 304: 153: 120: 115: 124: 416: 270: 252: 160: 149: 145: 20: 375: 141: 71: 54: 164: 107:
described above, it has xylose units di-substituted with 2 and 3-linked
100: 79: 50: 261: 137: 66: 27: 159:
Arabinoxylans are one of the main components of soluble and insoluble
108: 45:. The term arabinoxylan usually refers to feruloyl-arabinoxylan from 42: 91:
These feruloyl units can undergo radical oxidative coupling forming
96: 75: 46: 35: 317:
Wakabayashi K, et al (2005). Physiologia Plantarum. 125:127–134
62: 31: 38: 23: 218:
Scheller, H. V., & Ulvskov, P. (2010). Hemicelluloses.
234: 136:
Arabinoxylans chiefly serve a structural role in the
140:. They are also the reservoirs of large amounts of 414: 353: 326: 290: 388: 241:Journal of Agricultural and Food Chemistry 260: 224:doi:10.1146/annurev-arplant-042809-112315 34:contains substantial amounts of another 26:found in both the primary and secondary 191:. University of Georgia. Archived from 415: 214: 212: 210: 53:containing moieties of the phenolic 13: 220:Annual Review of Plant Biology, 61 14: 439: 207: 185:"Hemicellulosic Polysaccharides" 368:10.1016/j.phytochem.2005.09.036 30:of plants which in addition to 382: 347: 320: 311: 284: 228: 177: 1: 403:10.1016/s0963-9969(00)00038-7 341:10.1016/j.foodres.2008.04.001 305:10.1016/j.carbpol.2003.09.004 170: 131: 85: 7: 391:Food Research International 329:Food Research International 10: 444: 93:ferulic acid dehydrodimers 253:10.1021/acs.jafc.6b00103 293:Carbohydrate Polymers 61:(in the same way as 59:oxidative coupling 247:(14): 2883–2892. 195:on April 16, 2021 150:covalently linked 57:that can undergo 19:is a form of the 435: 407: 406: 397:(3–4): 233–245. 386: 380: 379: 351: 345: 344: 324: 318: 315: 309: 308: 288: 282: 281: 279: 277: 264: 232: 226: 216: 205: 204: 202: 200: 181: 154:fungal pathogens 443: 442: 438: 437: 436: 434: 433: 432: 423:Polysaccharides 413: 412: 411: 410: 387: 383: 352: 348: 325: 321: 316: 312: 289: 285: 275: 273: 233: 229: 217: 208: 198: 196: 183: 182: 178: 173: 134: 121:p-coumaric acid 116:glucuronic acid 88: 65:units) forming 12: 11: 5: 441: 431: 430: 425: 409: 408: 381: 356:Phytochemistry 346: 335:(9): 850–868. 319: 310: 299:(2): 171–177. 283: 227: 206: 175: 174: 172: 169: 161:dietary fibers 146:phenolic acids 133: 130: 125:sinapinic acid 87: 84: 9: 6: 4: 3: 2: 440: 429: 426: 424: 421: 420: 418: 404: 400: 396: 392: 385: 377: 373: 369: 365: 361: 357: 350: 342: 338: 334: 330: 323: 314: 306: 302: 298: 294: 287: 272: 268: 263: 258: 254: 250: 246: 242: 238: 231: 225: 221: 215: 213: 211: 194: 190: 186: 180: 176: 168: 166: 162: 157: 155: 151: 147: 143: 139: 129: 126: 122: 117: 112: 110: 104: 102: 98: 94: 83: 81: 77: 73: 68: 64: 60: 56: 52: 48: 44: 40: 37: 33: 29: 25: 22: 21:hemicellulose 18: 394: 390: 384: 359: 355: 349: 332: 328: 322: 313: 296: 292: 286: 274:. Retrieved 262:11586/173594 244: 240: 230: 219: 197:. Retrieved 193:the original 188: 179: 158: 142:ferulic acid 135: 113: 105: 89: 72:monophyletic 55:ferulic acid 17:Arabinoxylan 16: 15: 362:(1): 91–9. 222:, 263-289. 165:antioxidant 138:plant cells 51:commelinids 428:Copolymers 417:Categories 276:5 February 171:References 148:which are 144:and other 101:commelinid 99:and other 80:commelinid 78:and other 67:crosslinks 49:and other 28:cell walls 271:0021-8561 132:Functions 123:but also 109:arabinose 103:species. 86:Structure 82:species. 43:arabinose 376:16289622 199:April 1, 189:uga.edu 97:grasses 76:grasses 47:grasses 36:pentose 374:  269:  63:lignin 32:xylose 39:sugar 24:xylan 372:PMID 278:2023 267:ISSN 201:2020 399:doi 364:doi 337:doi 301:doi 257:hdl 249:doi 419:: 395:33 393:. 370:. 360:67 358:. 333:41 331:. 297:55 295:. 265:. 255:. 245:64 243:. 239:. 209:^ 187:. 156:. 41:, 405:. 401:: 378:. 366:: 343:. 339:: 307:. 303:: 280:. 259:: 251:: 203:.

Index

hemicellulose
xylan
cell walls
xylose
pentose
sugar
arabinose
grasses
commelinids
ferulic acid
oxidative coupling
lignin
crosslinks
monophyletic
grasses
commelinid
ferulic acid dehydrodimers
grasses
commelinid
arabinose
glucuronic acid
p-coumaric acid
sinapinic acid
plant cells
ferulic acid
phenolic acids
covalently linked
fungal pathogens
dietary fibers
antioxidant

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