» Articles » PMID: 1070006

Structure and Transformation of Chitin Synthetase Particles (chitosomes) During Microfibril Synthesis in Vitro

Overview
Specialty Science
Date 1976 Dec 1
PMID 1070006
Citations 36
Authors
Affiliations
Soon will be listed here.
Abstract

The fine structure of isolated chitin synthetase (UDP-2-acetamido-2-deoxy-D-glucose:chitin 4-beta-acetamido-deoxyglucosyltransferase; EC 2-4-1-16) particles (chitosomes) from Mucor rouxii and the elaboration of chitin microfibrils were studied by electron microscopy. Chitosomes are spheroidal, but often polymorphic, structures, mostly 40-70 nm in diameter. Their appearance after negative staining varies. Some reveal internal granular structure enclosed by a shell measuring 6-12 nm thick; others do not show internal structure but have a pronounced depression of the external surface. In thin sections, isolated chitosomes appear as microvesicular structures with a tripartite shell 6.5-7.0 nm thick. Morphologically similar structures can be seen in intact cells of M. rouxii. Isolated chitosomes undergo a seemingly irreversible series of transformations when substrate and activators are added. The internal structure changes, and a coiled microfibril (fibroid) appears inside the chitosome. The shell of the chitosome is opened or shed, and an extended microfibril arises from the fibroid particle. During prolonged incubation, the fibroid coils become less common and extended microfibrils appear thicker. We regard the chitosome as the cytoplasmic container and conveyor of chitin synthetase en route to its destination at the cell surface. Isolated chitosomes are well suited for integrated ultrastructural-biochemical studies of microfibril biogenesis in vitro.

Citing Articles

Chitin Biosynthesis in Species.

Brauer V, Pessoni A, Freitas M, Cavalcanti-Neto M, Ries L, Almeida F J Fungi (Basel). 2023; 9(1).

PMID: 36675910 PMC: 9865612. DOI: 10.3390/jof9010089.


Nanochitin: Chemistry, Structure, Assembly, and Applications.

Bai L, Liu L, Esquivel M, Tardy B, Huan S, Niu X Chem Rev. 2022; 122(13):11604-11674.

PMID: 35653785 PMC: 9284562. DOI: 10.1021/acs.chemrev.2c00125.


Recent Advances in Electron Microscopy of Carbohydrate Nanoparticles.

Ogawa Y, Putaux J Front Chem. 2022; 10:835663.

PMID: 35242740 PMC: 8886399. DOI: 10.3389/fchem.2022.835663.


The MIT domain of chitin synthase 1 from the oomycete interacts specifically with phosphatidic acid.

Brown C, Patrick J, Liebau J, Maler L Biochem Biophys Rep. 2022; 30:101229.

PMID: 35198741 PMC: 8851075. DOI: 10.1016/j.bbrep.2022.101229.


Wide distribution of the -bacterium endosymbiosis in naturally infected maize plants.

Perez-Rodriguez F, Gonzalez-Prieto J, Vera-Nunez J, Ruiz-Medrano R, Pena-Cabriales J, Ruiz-Herrera J Plant Signal Behav. 2020; 16(2):1855016.

PMID: 33356903 PMC: 7849723. DOI: 10.1080/15592324.2020.1855016.


References
1.
Brown Jr R, Montezinos D . Cellulose microfibrils: visualization of biosynthetic and orienting complexes in association with the plasma membrane. Proc Natl Acad Sci U S A. 1976; 73(1):143-7. PMC: 335856. DOI: 10.1073/pnas.73.1.143. View

2.
CABIB E, Ulane R, Bowers B . A molecular model for morphogenesis: the primary septum of yeast. Curr Top Cell Regul. 1974; 8(0):1-32. DOI: 10.1016/b978-0-12-152808-9.50008-0. View

3.
Reed L, Oliver R . The multienzyme alpha-keto acid dehydrogenase complexes. Brookhaven Symp Biol. 1968; 21(2):397-412. View

4.
Ray P, Shininger T, RAY M . ISOLATION OF beta-GLUCAN SYNTHETASE PARTICLES FROM PLANT CELLS AND IDENTIFICATION WITH GOLGI MEMBRANES. Proc Natl Acad Sci U S A. 1969; 64(2):605-12. PMC: 223387. DOI: 10.1073/pnas.64.2.605. View

5.
Ruiz-Herrera J, Sing V, Van Der Woude W, Bartnicki-Garcia S . Microfibril assembly by granules of chitin synthetase. Proc Natl Acad Sci U S A. 1975; 72(7):2706-10. PMC: 432839. DOI: 10.1073/pnas.72.7.2706. View