APPROACHES TO INFLUENCE STARCH QUANTITY AND STARCH QUALITY IN TRANSGENIC PLANTS

被引:36
作者
MULLERROBER, B
KOSSMANN, J
机构
[1] Institut Für Genbiologische Forschung Berlin Gmbh, Berlin, 14195
关键词
ADP-GLUCOSE PYROPHOSPHORYLASE; STARCH SYNTHASE; BRANCHING ENZYME; STARCH QUALITY (STRUCTURE); STARCH QUANTITY; TRANSGENIC PLANTS; SOLANUM TUBEROSUM;
D O I
10.1111/j.1365-3040.1994.tb00152.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Starch plays a major role as a transitory and long-term storage compound in higher plants, and therefore is of prime importance for plant growth and development. Additionally, starch serves as a widely used material for a variety of industrial uses. The formation of starch can arbitrarily be divided into three types of event: (I) those leading to the supply of glucose-1-phosphate in the plastids; (II) the conversion of glucose-1-phosphate to ADP-glucose catalysed by the enzyme ADP-glucose pyrophosphorylase; and (m) the enzymatic reactions converting ADP-glucose to long-chain glucans (amylopectin, amylose). In recent years, numerous cDNA and genomic sequences encoding enzymes involved in starch metabolism have been identified. Some of these have been used to down-regulate enzyme activities via the antisense RNA technique. Additionally, bacterial genes have been ectopically expressed in transgenic plants in order to increase corresponding enzyme activities. By modulating the activity of ADP-glucose pyrophosphorylase in plastids, it was possible to decrease and increase, respectively, the starch content in source and sink organs of transgenic plants. In addition, down-regulation of granule-bound starch synthase (isoform I) resulted in the production of starch that was almost completely free of amylose. Further experiments aimed to modulate starch structure are currently underway and will briefly be discussed.
引用
收藏
页码:601 / 613
页数:13
相关论文
共 94 条
[1]   ISOLATION AND ANALYSIS OF A CDNA CLONE ENCODING THE SMALL-SUBUNIT OF ADP-GLUCOSE PYROPHOSPHORYLASE FROM WHEAT [J].
AINSWORTH, C ;
TARVIS, M ;
CLARK, J .
PLANT MOLECULAR BIOLOGY, 1993, 23 (01) :23-33
[2]  
ANDERSON JM, 1989, J BIOL CHEM, V264, P12238
[3]   MOLECULAR CHARACTERIZATION OF THE GENE ENCODING A RICE ENDOSPERM-SPECIFIC ADPGLUCOSE PYROPHOSPHORYLASE SUBUNIT AND ITS DEVELOPMENTAL PATTERN OF TRANSCRIPTION [J].
ANDERSON, JM ;
LARSEN, R ;
LAUDENCIA, D ;
KIM, WT ;
MORROW, D ;
OKITA, TW ;
PREISS, J .
GENE, 1991, 97 (02) :199-205
[4]  
APREES T, 1992, ENV PLANT B, P115
[5]   SEQUENCE CONSERVATION OF THE CATALYTIC REGIONS OF AMYLOLYTIC ENZYMES IN MAIZE BRANCHING ENZYME-I [J].
BABA, T ;
KIMURA, K ;
MIZUNO, K ;
ETOH, H ;
ISHIDA, Y ;
SHIDA, O ;
ARAI, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 181 (01) :87-94
[6]  
BAE JM, 1990, MAYDICA, V35, P317
[7]   TOWARD A SCIENCE OF METABOLIC ENGINEERING [J].
BAILEY, JE .
SCIENCE, 1991, 252 (5013) :1668-1675
[8]  
BALL S, 1991, PLANTA, V185, P17, DOI 10.1007/BF00194509
[9]   PHYSIOLOGY OF STARCH STORAGE IN THE MONOCELLULAR ALGA CHLAMYDOMONAS-REINHARDTII [J].
BALL, SG ;
DIRICK, L ;
DECQ, A ;
MARTIAT, JC ;
MATAGNE, RF .
PLANT SCIENCE, 1990, 66 (01) :1-9
[10]   IDENTIFICATION AND MOLECULAR CHARACTERIZATION OF SHRUNKEN-2 CDNA CLONES OF MAIZE [J].
BHAVE, MR ;
LAWRENCE, S ;
BARTON, C ;
HANNAH, LC .
PLANT CELL, 1990, 2 (06) :581-588