Views
3 years ago

Preface - kmutt

Preface - kmutt

KMUTT Annual Research

KMUTT Annual Research Abstracts 2005 begins with the fixation of CO 2 from atmosphere to the Calvin cycle. Passing through a series of reactions, triose phosphate from Calvin cycle is converted to sucrose which is transported to sink cells and is eventually formed the amylose and amylopectin (starch constituents). After validating the model with data from a number of literatures, the results show that the structured model is a good representative of studied system. The result of triose phosphate (DHAP and GAP) elevation due to lessening the aldolase activity is an illustration of validation. Furthermore, the representative model will be used to gain more understanding of starch production process such as the effect of CO 2 uptake on qualitative and quantitative aspects of starch biosynthesis. IC-322 AN APPLIED PROCESS CONTROL CONCEPT TO GENE MOTIF NETWORK MODELING FOR PREDICTING THE GENE EXPRESSION PROFILES Saowalak Kalapanulak, Natee Tang-amornsuksan, Asawin Meechai, Supapon Cheevadhanarak, Sakarindr Bhumiratana Bioinfo 2005 (the 2005 International Joint Conference of InCoB, AASBi and KSBI), September 22-24, 2005, BEXCO, Busan, Korea In this work, we applied the transfer function commonly used in process control theory to model and predict the expression of genes within a given regulatory motif of Saccharomyces cerevisiae. To demonstrate this technique, the cell cycle microarray data of S. cerevisiae at alpha-factor arrest condition obtained from literatures were used. The transfer function model of a feed-forward motif was created using two methods; i.e, the modified Gene Kim’s and the Control Station Software methods. The former required to express the array data as mathematical equations before formulating the transfer function, whereas the latter used the array data as input into the software to obtain the function. In comparison, the modified Gene Kim’s method provided a better transfer function model. This model can predict the expression data of CUP9 and YJR100C genes of fkh1, fkh2 mutant S. cerevisiae strains within 20% error. This model can predict not only the expression of the target genes but also the expression of the regulator genes. Moreover, identification of the most 189 effective regulator genes in each network motif is possible. IC-323 PROBING STARCH BIOSYNTHESIS ENZYME ISOFORMS BY VISUALIZATION OF CONSERVED SECONDARY STRUCTURE PATTERNS Tayvich Vorapreeda, Weerayuth Kittichotirat, Asawin Meechai, Sakarindr Bhumiratana, Supapon Cheevadhanarak Bioinfo 2005 (the 2005 International Joint Conference of InCoB, AASBi and KSBI), September 22-24, 2005, BEXCO, Busan, Korea Starch is an indispensable raw material in many industries. The utilization of starch mostly depends on its physical and chemical properties, which differ according to plant origins and their varieties, and the manufacturers often find them unsuitable for their industrial requirement. These problems are often handled by exposing the native form of starch to physical or chemical modification processes in ordered to tailor them appropriately according to the industrial needs. However, both physical and chemical modifications are cost intensive and generate high chemical waste. Moreover, large portion of starches are likely to be destroyed during the process. Thus, a major challenge would be to predict the effect of genetic changes on the functional properties of starch to produce designer starches that suit specific uses. The enzymes in starch biosynthesis pathway generally have a variety of isoforms that have specific roles, which are believed to affect starch properties, but their precise roles have not been identified. Understanding of relationships between enzyme isofoms in starch biosynthesis processes and properties of starch granule is therefore one of the main goals of plant molecular biologists. Because of the difficulties in obtaining experimental evidences of each enzyme isoform, as they are usually instable, hard to purify to homogeneity and exist in low abundance, classifying them into families based on the presence of shared features is one of the common strategies for functional analysis. Additionally since structures are more conserved than sequences in evolution and with the evidence that secondary structure agreement between predicted secondary structures can be used to identify distantly related protein sequences, we present a novel computational method for reclassifying starch enzyme isoforms International Conference

190 based on predicted secondary structures. IC-324 IN SILICO DISCOVERY OF SUBSTRATE SPECIFICITY OF SOLUBLE STARCH SYNTHASE VIA SECONDARY STRUCTURE FEATURES Tayvich Vorapreeda, Weerayuth Kittichotirat, Kriengkrai Porkaew, Asawin Meechai, Sakarindr Bhumiratana, Supapon Cheevadhanarak Starch Update 2005 : The 3 rd Conference on Starch Technology (BioThailand 2005), November 4-5, 2005, Queen Sirikit National Convention Center, Bangkok, Thailand, p. 388 The enzyme isoforms in starch biosynthesis pathway generally are believed to have a lot of influences on starch qualities and quantities. Understanding the relationships between enzyme isoforms and properties of starch is therefore of economical importance in the applications of starch in many industries. However, their precised roles have not been clearly identified by experimental approaches. Thus, we present a novel computational method for classifying and identifying starch enzyme isoforms based on predicted secondary structures. The method can automatically perform unsupervised cluster discovery from the secondary structure of starch biosynthesis enzyme isoforms data input based on their similarity. We applied our method to analyze a set of 36 soluble starch synthase isoforms, and found that the soluble starch synthase isoforms mostly contain structural regions that exhibit similar features in the C-terminal, with the distinctive features in the N-terminal region. The result suggests that the N-terminal variations (difference in both length and homology) in starch synthases may not directly involve in catalytic activity of these enzymes, but instead regulate the binding of glucose substrate to the enzymes. Furthermore, the N-terminus may play a role in targeting starch synthases to specific portions of the starch granule, and interacting with other enzymes in starch biosynthesis mechanism. IC-325 META-ANALYSIS OF THE TRANSCRIPTOME OF ARABIDOPSIS: A CHALLENGE IN STUDYING STARCH BIOSYNTHESIS IN HIGHER PLANTS Papapit Ingkasuwan, Sawannee Sutheeworapong, KMUTT Annual Research Abstracts 2005 Supatcharee Netrphan, Jeerayut Chaijaruwanich, Asawin Meechai, Supapon Cheevadhanarak, Sakarindr Bhumiratana Starch Update 2005 : The 3 rd Conference on Starch Technology (BioThailand 2005), November 4-5, 2005, Queen Sirikit National Convention Center, Bangkok, Thailand, p. 339 The transcriptome of Arabidopsis thaliana, a favorite plant model, is becoming an essential tool in the starch research. In this work, meta-analysis based on effect size methods was employed to extract global gene sets associated with the alteration of starch properties from multiple microarray data of A. thaliana grown under various environmental changes. This approach potentially yields sets of significant and differentially expressed genes and also voids the artifacts of individual studies. These gene sets and their expression profiles obtaining from meta-analysis were compared with the individual study. The results revealed that most of the significant global gene sets are outside the starch biosynthesis pathway, whereas only subtle changes in transcriptional profiles of most genes in starch biosynthesis under such conditions were observed. This indicates the complexity of regulatory systems of starch biosynthesis mechanism controlled by either the genes being external to the pathway or other levels of regulations, such as post-transcriptional regulation. The information of these coordinated genes may suggest multi-level of molecular mechanisms linked with the regulatory process in starch biosynthesis. With the appearance of novel algorithms and the sophisticated statistical tools for analyzing high-throughout data, this finding demonstrates the power of meta-analysis in generating new insight knowledge in starch metabolism of higher plant. IC-326 CASSAVA MOLECULAR BIOTECHNOLOGY CONSORTIUM (CASS- MOL-BIOTECH): A JOINT RESEARCH ON CASSAVA STARCH BIOSYNTHESIS IN THAILAND Supatcharee Netrphan, Malinee Suksanpanomrung, Yindee Chanvivattana, Sithichoke Tangphatsornruang, Tipaporn Limpaseni, Asawin Meechai, Kanokporn Triwitayakorn, Punchapat Sojikul, KittisakYokthongwattana, Jeerapun Worapong, Oranuch Bunseng, Supaporn Cheevadhanarak, International Conference

  • Page 2:

    ISBN 974-456-652-3

  • Page 6:

    CONTENTS Page Preface International

  • Page 10 and 11:

    KMUTT Annual Research Abstracts 200

  • Page 12 and 13:

    KMUTT Annual Research Abstracts 200

  • Page 14 and 15:

    KMUTT Annual Research Abstracts 200

  • Page 16 and 17:

    KMUTT Annual Research Abstracts 200

  • Page 18 and 19:

    KMUTT Annual Research Abstracts 200

  • Page 20 and 21:

    KMUTT Annual Research Abstracts 200

  • Page 22 and 23:

    KMUTT Annual Research Abstracts 200

  • Page 24 and 25:

    KMUTT Annual Research Abstracts 200

  • Page 26 and 27:

    KMUTT Annual Research Abstracts 200

  • Page 28 and 29:

    KMUTT Annual Research Abstracts 200

  • Page 30 and 31:

    KMUTT Annual Research Abstracts 200

  • Page 32 and 33:

    KMUTT Annual Research Abstracts 200

  • Page 34 and 35:

    KMUTT Annual Research Abstracts 200

  • Page 36 and 37:

    KMUTT Annual Research Abstracts 200

  • Page 38 and 39:

    KMUTT Annual Research Abstracts 200

  • Page 40 and 41:

    KMUTT Annual Research Abstracts 200

  • Page 42 and 43:

    KMUTT Annual Research Abstracts 200

  • Page 44 and 45:

    KMUTT Annual Research Abstracts 200

  • Page 46 and 47:

    KMUTT Annual Research Abstracts 200

  • Page 48 and 49:

    KMUTT Annual Research Abstracts 200

  • Page 50 and 51:

    KMUTT Annual Research Abstracts 200

  • Page 52 and 53:

    KMUTT Annual Research Abstracts 200

  • Page 54 and 55:

    KMUTT Annual Research Abstracts 200

  • Page 56 and 57:

    KMUTT Annual Research Abstracts 200

  • Page 58:

    National Journals

  • Page 61 and 62:

    54 นอยกวาแบบต

  • Page 63 and 64:

    56 (Least Square Matching Method)

  • Page 65 and 66:

    58 อุณหภูมิ 30 แ

  • Page 67 and 68:

    60 สเปกตรัม จา

  • Page 69 and 70:

    62 ขอมูลดานทร

  • Page 71 and 72:

    64 22.8 มาตรฐานเป

  • Page 73 and 74:

    66 2545 NJ-033 EFFECTS OF ELEVATED

  • Page 75 and 76:

    68 เปลือกที่ม

  • Page 77 and 78:

    70 ของการดูดซ

  • Page 79 and 80:

    72 การสกัดดวย

  • Page 81 and 82:

    74 collection of authentic texts th

  • Page 83 and 84:

    76 รอยละ 32 มีสา

  • Page 86 and 87:

    KMUTT Annual Research Abstracts 200

  • Page 88 and 89:

    KMUTT Annual Research Abstracts 200

  • Page 90 and 91:

    KMUTT Annual Research Abstracts 200

  • Page 92 and 93:

    KMUTT Annual Research Abstracts 200

  • Page 94 and 95:

    KMUTT Annual Research Abstracts 200

  • Page 96 and 97:

    KMUTT Annual Research Abstracts 200

  • Page 98 and 99:

    KMUTT Annual Research Abstracts 200

  • Page 100 and 101:

    KMUTT Annual Research Abstracts 200

  • Page 102 and 103:

    KMUTT Annual Research Abstracts 200

  • Page 104 and 105:

    KMUTT Annual Research Abstracts 200

  • Page 106 and 107:

    KMUTT Annual Research Abstracts 200

  • Page 108 and 109:

    KMUTT Annual Research Abstracts 200

  • Page 110 and 111:

    KMUTT Annual Research Abstracts 200

  • Page 112 and 113:

    KMUTT Annual Research Abstracts 200

  • Page 114 and 115:

    KMUTT Annual Research Abstracts 200

  • Page 116 and 117:

    KMUTT Annual Research Abstracts 200

  • Page 118 and 119:

    KMUTT Annual Research Abstracts 200

  • Page 120 and 121:

    KMUTT Annual Research Abstracts 200

  • Page 122 and 123:

    KMUTT Annual Research Abstracts 200

  • Page 124 and 125:

    KMUTT Annual Research Abstracts 200

  • Page 126 and 127:

    KMUTT Annual Research Abstracts 200

  • Page 128 and 129:

    KMUTT Annual Research Abstracts 200

  • Page 130 and 131:

    KMUTT Annual Research Abstracts 200

  • Page 132 and 133:

    KMUTT Annual Research Abstracts 200

  • Page 134 and 135:

    KMUTT Annual Research Abstracts 200

  • Page 136 and 137:

    KMUTT Annual Research Abstracts 200

  • Page 138 and 139:

    KMUTT Annual Research Abstracts 200

  • Page 140 and 141:

    KMUTT Annual Research Abstracts 200

  • Page 142 and 143:

    KMUTT Annual Research Abstracts 200

  • Page 144 and 145:

    KMUTT Annual Research Abstracts 200

  • Page 146 and 147: KMUTT Annual Research Abstracts 200
  • Page 148 and 149: KMUTT Annual Research Abstracts 200
  • Page 150 and 151: KMUTT Annual Research Abstracts 200
  • Page 152 and 153: KMUTT Annual Research Abstracts 200
  • Page 154 and 155: KMUTT Annual Research Abstracts 200
  • Page 156 and 157: KMUTT Annual Research Abstracts 200
  • Page 158 and 159: KMUTT Annual Research Abstracts 200
  • Page 160 and 161: KMUTT Annual Research Abstracts 200
  • Page 162 and 163: KMUTT Annual Research Abstracts 200
  • Page 164 and 165: KMUTT Annual Research Abstracts 200
  • Page 166 and 167: KMUTT Annual Research Abstracts 200
  • Page 168 and 169: KMUTT Annual Research Abstracts 200
  • Page 170 and 171: KMUTT Annual Research Abstracts 200
  • Page 172 and 173: KMUTT Annual Research Abstracts 200
  • Page 174 and 175: KMUTT Annual Research Abstracts 200
  • Page 176 and 177: KMUTT Annual Research Abstracts 200
  • Page 178 and 179: KMUTT Annual Research Abstracts 200
  • Page 180 and 181: KMUTT Annual Research Abstracts 200
  • Page 182 and 183: KMUTT Annual Research Abstracts 200
  • Page 184 and 185: KMUTT Annual Research Abstracts 200
  • Page 186 and 187: KMUTT Annual Research Abstracts 200
  • Page 188 and 189: KMUTT Annual Research Abstracts 200
  • Page 190 and 191: KMUTT Annual Research Abstracts 200
  • Page 192 and 193: KMUTT Annual Research Abstracts 200
  • Page 194 and 195: KMUTT Annual Research Abstracts 200
  • Page 198 and 199: KMUTT Annual Research Abstracts 200
  • Page 200 and 201: KMUTT Annual Research Abstracts 200
  • Page 202 and 203: KMUTT Annual Research Abstracts 200
  • Page 204 and 205: KMUTT Annual Research Abstracts 200
  • Page 206 and 207: KMUTT Annual Research Abstracts 200
  • Page 208 and 209: KMUTT Annual Research Abstracts 200
  • Page 210 and 211: KMUTT Annual Research Abstracts 200
  • Page 212 and 213: KMUTT Annual Research Abstracts 200
  • Page 214: National Conferences
  • Page 217 and 218: 210 จอมเทียนปา
  • Page 219 and 220: 212 การสกัดสาร
  • Page 221 and 222: 214 ไดแก อุณหภู
  • Page 223 and 224: 216 โดยกลไกของ
  • Page 225 and 226: 218 เคลือบเมื่
  • Page 227 and 228: 220 สําเริง จัก
  • Page 229 and 230: 222 ลดเวลาตลอด
  • Page 231 and 232: 224 อุณหภูมิสู
  • Page 233 and 234: 226 NC-043 การวิเคร
  • Page 235 and 236: 228 เกิดพฤติกร
  • Page 237 and 238: 230 เดียว เพื่อ
  • Page 239 and 240: 232 มากนอยเพีย
  • Page 241 and 242: 234 หลักที่พบใ
  • Page 243 and 244: 236 NC-073 การออกแบ
  • Page 245 and 246: 238 บทความนี้น
  • Page 247 and 248:

    240 นําเอาเวคเ

  • Page 249 and 250:

    242 งานวิจัยนี

  • Page 251 and 252:

    244 การอบแหงลด

  • Page 253 and 254:

    246 แยกเฟสต่ํา

  • Page 255 and 256:

    248 กลบ โดยเปรี

  • Page 257 and 258:

    250 นํามาใช คือ

  • Page 259 and 260:

    252 วิเคราะหหา

  • Page 261 and 262:

    254 NC-123 การวิเคร

  • Page 263 and 264:

    256 NC-129 เครื่องผ

  • Page 265 and 266:

    258 สามารถขยาย

  • Page 267 and 268:

    260 ครั้งที่ 43, 1-

  • Page 269 and 270:

    262 calculated with the use of the

  • Page 271 and 272:

    264 Version 1.3.1 และ Softwar

  • Page 273 and 274:

    266 ขนไกได จากก

  • Page 275 and 276:

    268 โครงสรางขอ

  • Page 277 and 278:

    270 การปลูกพืช

  • Page 279 and 280:

    272 ระดับพึงพอ

  • Page 281 and 282:

    274 ของแกสโซฮอ

  • Page 283 and 284:

    276 1) สภาพทั่วไ

  • Page 285 and 286:

    278 อนุปริญญา แ

  • Page 287 and 288:

    280 อาชีวศึกษา

  • Page 289 and 290:

    282 กระทบตอคุณ

  • Page 291 and 292:

    284 ตั้งกลไกแข

  • Page 293 and 294:

    286 นุชจรินทร เ

  • Page 295 and 296:

    288 โดยรวมผูบร

  • Page 297 and 298:

    290 แนนกระแสไฟ

  • Page 299 and 300:

    292 NC-222 ผลงานตีพ

  • Page 301 and 302:

    294 NC-227 เตาเผาไห

  • Page 303 and 304:

    296 จําเพาะรวม

  • Page 305 and 306:

    298 NC-238 จลนพลศาส

  • Page 307 and 308:

    300 ทนงเกียรติ

  • Page 309 and 310:

    302 ดีเซลนั้นม

  • Page 311 and 312:

    304 NC-254 การใชเทค

  • Page 313 and 314:

    306 อาคารศูนยก

  • Page 315 and 316:

    308 กระบวนการร

  • Page 317 and 318:

    310 บรรยากาศขอ

  • Page 319 and 320:

    312 metal ions on 2-AP biosyntheis

  • Page 321 and 322:

    314 total clones while the ethanol

  • Page 323 and 324:

    316 การประชุมท

  • Page 325 and 326:

    318 BioThailand (The 16 th Annual M

  • Page 327 and 328:

    320 สูงที่สุดพ

  • Page 329 and 330:

    322 นัยสําคัญท

  • Page 331 and 332:

    324 ความเขมขนร

  • Page 333 and 334:

    326 ปลูกแบบพรา

  • Page 335 and 336:

    328 นี้ทําใหทร

  • Page 337 and 338:

    330 ดุลชาติ มาน

  • Page 339 and 340:

    332 ไมโครเมตร ส

  • Page 341 and 342:

    334 In this study, we collected seq

  • Page 343 and 344:

    336 กนกรัตน นาค

  • Page 345 and 346:

    338 การพัฒนาสื

  • Page 347 and 348:

    340 one of the causes of difficulty

  • Page 349 and 350:

    342 ทวีรัตน วิจ

  • Page 351 and 352:

    344 program, Cytoscape. This model

  • Page 353 and 354:

    346 production demand. Nevertheless

  • Page 355 and 356:

    348 อุลตราไวโอ

  • Page 357 and 358:

    350 นี้อยูในชว

  • Page 359 and 360:

    352 เพื่อนําสว

  • Page 361 and 362:

    354 trichloroacetic acid (TCA) ม

  • Page 363 and 364:

    356 ทรัพยากรที

  • Page 365 and 366:

    358 ในประเทศสห

  • Page 367 and 368:

    360 8-9 ธันวาคม 2548,

  • Page 369 and 370:

    362 ซึ่งเกิดขอ

  • Page 371 and 372:

    364 NC-391 การวิเคร

  • Page 373 and 374:

    366 การประชุมว

  • Page 375 and 376:

    368 2547) พบวามหาว

  • Page 377 and 378:

    370 กนกพร ลีลาเ

  • Page 380:

    Authors Index

  • Page 383 and 384:

    376 จงจิตร หิรั

  • Page 385 and 386:

    378 ธ ธนธร ทองส

  • Page 387 and 388:

    380 พยุงศักดิ์

  • Page 389 and 390:

    382 วรรณพ วิเศษ

  • Page 391 and 392:

    384 สุดารัตน จิ

  • Page 393 and 394:

    386 อุลาวัณย กุ

  • Page 395 and 396:

    388 138, 141, 142 Jarunya Narangaja

  • Page 397 and 398:

    390 Panida Kongsawadworakul 191 Pan

  • Page 399 and 400:

    392 Sorakrich Maneewan 124, 136 Sor

  • Page 401 and 402:

    394 KMUTT Annual Research Abstracts

  • Page 404 and 405:

    KMUTT Annual Research Abstracts 200

  • Page 406 and 407:

    KMUTT Annual Research Abstracts 200

  • Page 408 and 409:

    KMUTT Annual Research Abstracts 200

  • Page 410 and 411:

    KMUTT Annual Research Abstracts 200

  • Page 412 and 413:

    KMUTT Annual Research Abstracts 200

  • Page 414 and 415:

    KMUTT Annual Research Abstracts 200

  • Page 416 and 417:

    KMUTT Annual Research Abstracts 200

  • Page 418 and 419:

    KMUTT Annual Research Abstracts 200

  • Page 420 and 421:

    KMUTT Annual Research Abstracts 200

  • Page 422 and 423:

    KMUTT Annual Research Abstracts 200

  • Page 424 and 425:

    KMUTT Annual Research Abstracts 200

  • Page 426 and 427:

    KMUTT Annual Research Abstracts 200

  • Page 428 and 429:

    KMUTT Annual Research Abstracts 200

  • Page 430 and 431:

    KMUTT Annual Research Abstracts 200

  • Page 432 and 433:

    KMUTT Annual Research Abstracts 200

  • Page 434 and 435:

    KMUTT Annual Research Abstracts 200

  • Page 436 and 437:

    KMUTT Annual Research Abstracts 200

  • Page 438 and 439:

    KMUTT Annual Research Abstracts 200

  • Page 440 and 441:

    KMUTT Annual Research Abstracts 200

  • Page 442 and 443:

    KMUTT Annual Research Abstracts 200

  • Page 444 and 445:

    KMUTT Annual Research Abstracts 200

  • Page 446 and 447:

    KMUTT Annual Research Abstracts 200

  • Page 448:

    KMUTT Annual Research Abstracts 200

  • Page 452:

    KMUTT Annual Research Abstracts 200

PE - kmutt