Autohydrolysis of birch wood

Holzforschung ◽  
2011 ◽  
Vol 65 (4) ◽  
Author(s):  
Lidia Testova ◽  
Sun-Li Chong ◽  
Maija Tenkanen ◽  
Herbert Sixta

Abstract Autohydrolysis of wood as a pretreatment stage before alkaline pulping is seen as an opportunity to approach the ideals of a forest biorefinery. In autohydrolysis the degradation products of primarily hemicelluloses and some other wood components are mainly dissolved (liquid phase) and they also escape partly as gas. In the present paper, birch was autohydrolysed at two intensity levels (characterised by P-factors of 200 and 1000) and the mass balances of autohydrolysis including solid, liquid, and gaseous phases were established. Approximately 10% and 25% of the total wood substance was transferred to the liquid phase at the two autohydrolysis intensities, respectively. In both cases about 50% of the degraded wood substance consisted of xylose-based material. The share of monomeric xylose was about 6% and 50% in the two samples, respectively. From the residual oligosaccharide fractions, 13% and 90% accounted for the DP2 to DP4 components in the P200 and P1000 samples, respectively. As expected, the weight-average molar mass of the components in the P1000 hydrolysate was substantially lower (0.4 kDa) than those in the corresponding P200 hydrolysate (2.1 kDa). Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) measurements revealed that relative to xylotriose the P1000 sample contained significantly fewer acidic pentosan fractions than the P200 sample. Xylooligosaccharides dissolved at both intensity levels remained highly acetylated, and some of these also carried 4-O-methylglucopyranosyluronic acid substituents.

2021 ◽  
Vol 54 (1) ◽  
pp. 52
Author(s):  
Udijanto Tedjosasongko ◽  
Dwi Mulia Ramadhaniati ◽  
Seno Pradopo

Background: Streptococcus mutans (S. mutans) bacteria mainly cause dental caries in children. These bacteria are not considered oral indigenous bacteria since they are transmitted from people around children during their deciduous teeth eruption. The detection of these bacteria can be used for dental caries prevention in children. Purpose: To determine the strain and serotype of S. mutans by using matrix assisted laser desorption ionization – time of flight mass spectrometry (MALDI-TOF MS) and polymerase chain reaction (PCR) on dental plaque samples taken from mother-child pairs. Methods: Sixteen dental plaque samples of mother-child pairs were cultured on brain heart infusion broth (BHIB) and mitis salivarius bacitracin (MSB) media until S. mutans colony isolates were obtained. Next, the isolates of S. mutans colony were introduced into the target plates of MALDI-TOF MS, and then ionized to become peptide mass fingerprint (PMF). Afterwards, the colony isolates were detected by database software. The detected S. mutans DNA then was extracted by using conventional 727 bp PCR (serotype C). Results: Six strains of S. mutans were detected by MALDI-TOF MS method. Five samples were classified into UA159, two samples were 3SN1, two samples were NFSM1, two samples were 11A1, two samples were U138, two samples were 4SM1, and one sample was classified into another bacterium. Five out of 16 samples were detected by PCR as serotype C (UA159). Conclusion: Six strains of S. mutans were detected, namely UA159, 3SN1, NFSM1, 11A1, U138, and 4SM1, one of them (UA159) was detected as serotype C.


Sign in / Sign up

Export Citation Format

Share Document