Chou Chung-Jung, Shockley Keith R, Conners Shannon B, Lewis Derrick L, Comfort Donald A, Adams Michael W W, Kelly Robert M
Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695-7905, USA.
Appl Environ Microbiol. 2007 Nov;73(21):6842-53. doi: 10.1128/AEM.00597-07. Epub 2007 Sep 7.
Glycoside linkage (cellobiose versus maltose) dramatically influenced bioenergetics to different extents and by different mechanisms in the hyperthermophilic archaeon Pyrococcus furiosus when it was grown in continuous culture at a dilution rate of 0.45 h(-1) at 90 degrees C. In the absence of S(0), cellobiose-grown cells generated twice as much protein and had 50%-higher specific H(2) generation rates than maltose-grown cultures. Addition of S(0) to maltose-grown cultures boosted cell protein production fourfold and shifted gas production completely from H(2) to H(2)S. In contrast, the presence of S(0) in cellobiose-grown cells caused only a 1.3-fold increase in protein production and an incomplete shift from H(2) to H(2)S production, with 2.5 times more H(2) than H(2)S formed. Transcriptional response analysis revealed that many genes and operons known to be involved in alpha- or beta-glucan uptake and processing were up-regulated in an S(0)-independent manner. Most differentially transcribed open reading frames (ORFs) responding to S(0) in cellobiose-grown cells also responded to S(0) in maltose-grown cells; these ORFs included ORFs encoding a membrane-bound oxidoreductase complex (MBX) and two hypothetical proteins (PF2025 and PF2026). However, additional genes (242 genes; 108 genes were up-regulated and 134 genes were down-regulated) were differentially transcribed when S(0) was present in the medium of maltose-grown cells, indicating that there were different cellular responses to the two sugars. These results indicate that carbohydrate characteristics (e.g., glycoside linkage) have a major impact on S(0) metabolism and hydrogen production in P. furiosus. Furthermore, such issues need to be considered in designing and implementing metabolic strategies for production of biofuel by fermentative anaerobes.
当嗜热古菌激烈火球菌在90℃下以0.45 h⁻¹的稀释率进行连续培养时,糖苷键(纤维二糖与麦芽糖)通过不同机制在不同程度上显著影响生物能量学。在没有硫单质(S(0))的情况下,以纤维二糖为碳源生长的细胞产生的蛋白质是麦芽糖生长培养物的两倍,且比麦芽糖生长培养物的比产氢速率高50%。向以麦芽糖为碳源生长的培养物中添加硫单质使细胞蛋白质产量提高了四倍,并使气体产生完全从氢气转变为硫化氢。相比之下,在以纤维二糖为碳源生长的细胞中存在硫单质仅使蛋白质产量增加了1.3倍,并且从产氢到产硫化氢的转变不完全,生成的氢气是硫化氢的2.5倍。转录响应分析表明,许多已知参与α-或β-葡聚糖摄取和加工的基因和操纵子以不依赖硫单质的方式上调。在以纤维二糖为碳源生长的细胞中,大多数对硫单质有差异转录反应的开放阅读框(ORF)在以麦芽糖为碳源生长的细胞中对硫单质也有反应;这些ORF包括编码膜结合氧化还原酶复合物(MBX)和两种假设蛋白(PF2025和PF2026)的ORF。然而,当硫单质存在于以麦芽糖为碳源生长的细胞培养基中时,有额外的基因(242个基因;108个基因上调,134个基因下调)发生了差异转录,这表明细胞对这两种糖有不同的反应。这些结果表明,碳水化合物特性(如糖苷键)对激烈火球菌中硫单质代谢和产氢有重大影响。此外,在设计和实施发酵厌氧菌生产生物燃料中的代谢策略时需要考虑这些问题。