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In this study, a novel strain for degrading chitin was identified as Bacillus paralicheniformis HL37, and the key chitinase CH1 was firstly mined through recombinant expression in Bacillus amyloliquefaciens HZ12. Subsequently, the sequence composition and catalytic mechanism of CH1 protein were analyzed. The molecular docking indicated that the triplet of Asp526, Asp528, and Glu530 was a catalytic active center. The enzymatic properties analysis revealed that the optimal reaction temperature and pH was 65 °C and 6.0, respectively. Especially, the chitinase activity showed no significant change below 55 °C and it could maintain over 60% activity after exposure to 85 °C for 30 min. Moreover, the optimal host strain and signal peptide were obtained to enhance the expression of chitinase CH1 significantly. As far as we know, it was the first time finding the highly efficient chitin-degrading enzymes in B. paralicheniformis, and detailed explanations were provided on the catalytic mechanism and enzymatic properties on CH1.

Mushroom dietary fiber is a type of bioactive macromolecule derived from the mycelia, fruiting bodies, or sclerotia of edible or medicinal fungi. The use of mushroom dietary fiber as a prebiotic has recently gained significant attention for providing health benefits to the host by promoting the growth of beneficial microorganisms; therefore, mushroom dietary fiber has promising prospects for application in the functional food industry and in drug development. This review summarizes methods for the preparation and modification of mushroom dietary fiber, its degradation and metabolism in the intestine, its impact on the gut microbiota community, and the generation of short-chain fatty acids (SCFAs); this review also systematically summarizes the beneficial effects of mushroom dietary fiber on host health. Overall, this review aims to provide theoretical guidance and a fresh perspective for the prebiotic application of mushroom dietary fiber in the development of new functional foods and drugs.

L-tyrosine is a key precursor for synthesis of various functional substances, but the microbial production of L-tyrosine faces huge challenges. The development of new microbial chassis cell and gene resource is especially important for the biosynthesis of L-tyrosine. In this study, the optimal host strain Bacillus amyloliquefaciens HZ-12 was firstly selected by detecting the production capacity of L-tyrosine. Subsequently, the recombinant expression of 15 prephenate dehydrogenase genes led to the discovery of the best gene, Bao-tyrA from B. amyloliquefaciens HZ-12. After the overexpression of Bao-tyrA, the L-tyrosine yield of the recombinant strain HZ/P43-Bao-tyrA reach 411 mg/L, increased by 42% compared with the control strain (HZ/pHY300PLK). Moreover, the nucleic acid sequence and deduced amino acid sequence of the gene Bao-tyrA were analyzed, and their conservative sites and catalytic mechanisms were proposed. Finally, the expression of Bao-tyrA was regulated through a promoter and 5′-UTR sequence to obtain the optimal expression elements. Thereby, the maximum L-tyrosine yield of 475 mg/L was obtained from HZ/P43-UTR3-Bao-tyrA. B. amyloliquefaciens was applied for the first time to produce L-tyrosine, and the optimal prephenate dehydrogenase gene Bao-tyrA and corresponding expression elements were obtained. This study provides new microbial host and gene resource for the construction of efficient L-tyrosine chassis cells, and also lays a solid foundation for the production of various functional tyrosine derivatives.

Grain yield (GY) prediction for wheat based on canopy spectral reflectance can improve selection efficiency in breeding programs. Time-series spectral information from different growth stages such as flowering to maturity is considered to have high accuracy in predicting GY and combining this information from multiple growth stages could effectively improve prediction accuracy. For this, 207 wheat cultivars and breeding lines were grown in full and limited irrigation treatments, and their canopy spectral reflectance was measured at the flowering, early, middle, and late grain fill stages. The potential of temporal spectral information at multiple growth stages for GY prediction was evaluated by a new method based on stacking the multiple growth stages data. Twenty VIs derived from spectral reflectance were used as the input feature of a support vector regression (SVR) to predict GY at each growth stage. The predicted GY values at multiple growth stages were trained by multiple linear regression (MLR) to establish a second-level prediction model. Results suggested that the prediction accuracy (R2) of VIs data from single growth stages ranged from 0.60 to 0.66 and 0.35 to 0.42 in the full and limited irrigation treatments, respectively. The prediction accuracy was increased by an average of 0.06, 0.07, and 0.07 after stacking the VIs of two, three, and four growth stages, respectively, under full irrigation. Similarly, under limited irrigation, the prediction accuracy was increased by 0.03, 0.04, and 0.04 by stacking the VIs of two, three, and four growth stages, respectively. Stacking of VIs of multiple important growth stages can increase the accuracy of GY prediction and application of a stable stacking model could increase the usefulness of data obtained from different phenotyping platforms.