Pillai Padmesh P, Nair Aswati R
Biotechnology and Bioinformatics Division, Jawaharlal Nehru Tropical Botanic Garden and Research Institute, Palode, Thiruvananthapuram 695 562, India.
School of Biotechnology, National Institute of Technology, Calicut 673 601, India.
C R Biol. 2014 Oct;337(10):571-80. doi: 10.1016/j.crvi.2014.08.002. Epub 2014 Sep 16.
The biochemical pathway to hypericin biosynthesis is presumed to be polyketide synthase (PKS) mediated, but it has not been experimentally validated, and no alternate route (chorismate/o-succinylbenzoate pathway) has been analyzed. We report here our earlier developed auxin inducible culture systems of Hypericum hookerianum as a model, to study the metabolic pathway to hypericin synthesis. Inhibitors of the alternate pathway at varying concentrations showed steady synthesis of total hypericins with means of 2.80±0.22, 18.75±0.01; 16.39±3.75, 29.60±1.90 (mevinolin) 2.53±0.10, 18.12±0.56; 0.14±0.01, 14.28±1.11 (fosmidomycin) and 2.7±0.35, 18.75±0.61; 0.14±0.01, 12.80±1.09 mg g(-1) DW (glyphosate) in the control and auxin-induced shoot and shoot-forming callus cultures, respectively. SSH analysis classified the differentially expressed sequences into protein synthesis (38%), modification (20%), electron transport (9%) and remaining as unclassified (11%) and unknown proteins (22%). Functional annotation of sequences indicates the presence of additional protein components besides PKS activity. Our results demonstrate direct biochemical and molecular evidence of PKS hypothesis of hypericin biosynthesis for the first time.
金丝桃素生物合成的生化途径据推测是由聚酮合酶(PKS)介导的,但尚未得到实验验证,且尚未分析其他途径(分支酸/邻琥珀酰苯甲酸途径)。我们在此报告我们早期开发的以滇金丝桃为模型的生长素诱导培养系统,用于研究金丝桃素合成的代谢途径。不同浓度的替代途径抑制剂在对照和生长素诱导的茎段及形成茎的愈伤组织培养物中显示出金丝桃素总量的稳定合成,其平均值分别为2.80±0.22、18.75±0.01;16.39±3.75、29.60±1.90(美伐他汀)2.53±0.10、18.12±0.56;0.14±0.01、14.28±1.11(磷霉素)以及2.7±0.35、18.75±0.61;0.14±0.01、12.80±1.09毫克/克干重(草甘膦)。抑制性消减杂交(SSH)分析将差异表达序列分为蛋白质合成(38%)、修饰(20%)、电子传递(9%),其余为未分类(11%)和未知蛋白质(22%)。序列的功能注释表明除了PKS活性外还存在其他蛋白质成分。我们的结果首次证明了金丝桃素生物合成的PKS假说的直接生化和分子证据。