Wu Leiming, Zhang Mingliang, Zhang Ran, Yu Haizhong, Wang Hailang, Li Jingyang, Wang Youmei, Hu Zhen, Wang Yanting, Luo Zi, Li Lin, Wang Lingqiang, Peng Liangcai, Xia Tao
Biomass & Bioenergy Research Centre, College of Plant Science & Technology, Huazhong Agricultural University, Wuhan, 430070, China.
National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan, China.
Biotechnol Biofuels. 2021 Dec 27;14(1):245. doi: 10.1186/s13068-021-02093-8.
As a major component of plant cell walls, cellulose provides the most abundant biomass resource convertible for biofuels. Since cellulose crystallinity and polymerization have been characterized as two major features accounting for lignocellulose recalcitrance against biomass enzymatic saccharification, genetic engineering of cellulose biosynthesis is increasingly considered as a promising solution in bioenergy crops. Although several transcription factors have been identified to regulate cellulose biosynthesis and plant cell wall formation, much remains unknown about its potential roles for genetic improvement of lignocellulose recalcitrance.
In this study, we identified a novel rice mutant (Osfc9/myb103) encoded a R2R3-MYB transcription factor, and meanwhile generated OsMYB103L-RNAi-silenced transgenic lines. We determined significantly reduced cellulose levels with other major wall polymers (hemicellulose, lignin) slightly altered in mature rice straws of the myb103 mutant and RNAi line, compared to their wild type (NPB). Notably, the rice mutant and RNAi line were of significantly reduced cellulose features (crystalline index/CrI, degree of polymerization/DP) and distinct cellulose nanofibers assembly. These alterations consequently improved lignocellulose recalcitrance for significantly enhanced biomass enzymatic saccharification by 10-28% at p < 0.01 levels (n = 3) after liquid hot water and chemical (1% HSO, 1% NaOH) pretreatments with mature rice straws. In addition, integrated RNA sequencing with DNA affinity purification sequencing (DAP-seq) analyses revealed that the OsMYB103L might specifically mediate cellulose biosynthesis and deposition by regulating OsCesAs and other genes associated with microfibril assembly.
This study has demonstrated that down-regulation of OsMYB103L could specifically improve cellulose features and cellulose nanofibers assembly to significantly enhance biomass enzymatic saccharification under green-like and mild chemical pretreatments in rice. It has not only indicated a powerful strategy for genetic modification of plant cell walls in bioenergy crops, but also provided insights into transcriptional regulation of cellulose biosynthesis in plants.
作为植物细胞壁的主要成分,纤维素提供了最丰富的可转化为生物燃料的生物质资源。由于纤维素结晶度和聚合度已被确定为导致木质纤维素对生物质酶解糖化具有抗性的两个主要特征,纤维素生物合成的基因工程越来越被视为生物能源作物的一种有前景的解决方案。尽管已经鉴定出几种转录因子来调节纤维素生物合成和植物细胞壁形成,但关于其在木质纤维素抗性遗传改良中的潜在作用仍有许多未知之处。
在本研究中,我们鉴定了一个编码R2R3-MYB转录因子的新型水稻突变体(Osfc9/myb103),同时构建了OsMYB103L-RNAi沉默转基因系。我们测定了在myb103突变体和RNAi系的成熟稻草中,纤维素水平显著降低,而其他主要细胞壁聚合物(半纤维素、木质素)略有改变,与野生型(NPB)相比。值得注意的是,水稻突变体和RNAi系的纤维素特征(结晶指数/CrI、聚合度/DP)显著降低,纤维素纳米纤维组装也不同。这些改变因此提高了木质纤维素的抗性,在对成熟稻草进行液体热水和化学(1%HSO、1%NaOH)预处理后,在p<0.01水平(n=3)下,生物质酶解糖化显著提高了10-28%。此外,综合RNA测序与DNA亲和纯化测序(DAP-seq)分析表明,OsMYB103L可能通过调节OsCesAs和其他与微纤丝组装相关的基因来特异性介导纤维素生物合成和沉积。
本研究表明,在水稻中进行类绿色和温和化学预处理时,下调OsMYB103L可特异性改善纤维素特征和纤维素纳米纤维组装,显著提高生物质酶解糖化。它不仅为生物能源作物中植物细胞壁的基因改造指明了一个有力策略,也为植物中纤维素生物合成的转录调控提供了见解。